Synthetic Hemorphin Analogs Containing Non-Natural Amino Acids: History
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Subjects: Chemistry, Organic | Chemistry, Medicinal | Chemistry, Analytical
Contributor:
Petar Todorov
,
Stela Georgieva
,
Jana Tchekalarova

The endogenous hemorphins are bioactive peptides with activity on opioid receptors. During the last decade, several research teams have synthesized, characterized, and pharmacologically evaluated synthetic hemorphin analogs containing unusual amino acids, D-amino acids, α-aminophosphonic acids, and their derivatives. The present review focuses on the structure-activity relationship analysis, details on specific methods for their characterization, and the advantage of synthetic hemorphin analogs compared to endogenous peptides as potent biologically active compounds with a complex mechanism of action.

  • hemorphins
  • non-natural amino acids
  • unusual amino acids
  • non-proteinogenic amino acids
  • biological activity
  • electrochemical behavior of peptides
  • characterization

1. Introduction

The endogenous peptides have biological activity and originate from precursor proteins via enzyme degradation in vesicles. They are released from the cell upon stimulation to function as neurotransmitters, hormones, and some short-chain peptides with unclear functions. Over the last decade, peptides derived from hemoglobin (Hb) have been extensively explored [1]. In the 1980s, endogenous opioid peptides were identified, leading to the isolation and characterization of Hb-active peptides with opioid-like effects [2]. The proteasomes and oligopeptides are enzymes producing hemoglobin (HB)-derived peptides with variable activities. These Hb-derived short-chain peptides consist of 4 to 10 amino acid residues, obtained from 35–38 and 35–39 fragments of β, γ, δ, and ε chains of Hb in humans, called hemorphins [3][4][5][6][7][8][9][10][11][12]. Hemorphins are endogenous peptides with opioid receptor affinity and morphinomimetic properties [13]. Several review articles have been written about hemorphins, including their isolation, purification, and structure–activity analysis [1][14][15]. Some of the structurally related hemorphins function as opioid receptor ligands with an affinity for µ-, δ-, and k-receptors and antinociceptive activity. In the peripheral nervous system, hemorphins affect cardiovascular, digestive, and endocrine functions. Some hemorphins play an essential role in the regulation of blood pressure by suppressing the activity of angiotensin-converting enzyme (ACE) and insulin-regulating aminopeptidase (IRAP).
The first known opioidergic peptide extracted from Hb (ß-chain 35–38) was hemorphin-4 with a possessed amino acid sequence: Tyr-Pro-Trp-Thr. By treating bovine blood with gastrointestinal enzymes with analytical techniques, its structure has been proven [16]. Hemorphin-4 can also be obtained by enzymatic hydrolysis of casein and Hb [17]. Yang et al. (1999) studied the effects of eight opioid tetrapeptides with similar amino acid sequences: endomorphin-1 (Tyr-Pro-Trp-Phe-NH2), endomorphin-2 (Tyr-Pro-Phe-Phe-NH2), morphiceptin (Tyr-Pro-Phe-Pro-NH2), hemorphin-4 (Tyr-Pro-Trp-Thr), Tyr-MIF-1 (Tyr-Pro-Leu-Gly-NH2), Tyr-W-MIF-1 (Tyr-Pro-Trp-Gly-NH2), TAPS (Tyr-D-Arg-Phe-Sar), and DALDA (Tyr-D-Arg-Phe-Lys-NH2), expressed in the rat locus coeruleus neurons whose brain structure is part of the reticular activating system involved in physiological responses to stress and panic [17]. All of these tetrapeptides spontaneously inhibited the tested neurons in the locus coeruleus. Hemorphin-4 has a similar structure and amino acid sequence close to that of endomorphins. Endomorphins have high affinity and selectivity for opioid receptors and are most responsible for the analgesic effects in the central nervous system. These properties of theirs are due to the presence of Pro, which represents a crucial factor for the structural and conformational properties of the ligand [18][19][20]. Proline plays the role of a stereochemical spacer capable of inducing a favorable spatial orientation of aromatic rings, which, in turn, is a crucial factor for ligand recognition and their interaction with the receptors. Therefore, the replacement of natural amino acids with other small non-natural amino acid modifications and their incorporation into opioid-based peptides have been the subject of intense research in recent years. Mollica et al. (2012, 2014, and 2015) performed detailed and valuable research on the use of various non-natural amino acid modifications as building blocks for drug discovery [18][19][20]. Thus, for example, the replacement of native proline with the divalent amino acid cis-4-amino-L-proline (cAmp) combining the conformational rigidity of the ring in opioid peptides can affect the stereochemistry of the entire molecule peptide, thereby leading to a significant increase in μ-opioid affinity and activity and to the correct fit of the peptide to the receptor [18][19][20]. Due to the interesting structural properties of the cAmp residue, its insertion into a peptide backbone can lead to both the usual linear analogs and some structurally interesting cyclical patterns. Conformational flexibility around Pro can be further enhanced by incorporating achiral analogs of Cα,α-disubstituted glycines, 1-aminocyclopentanecarboxylic acid (Ac5c), and 1-aminocyclohexanecarboxylic acid (Ac6c), etc. It should also be mentioned that the non-natural amino acid 2,6-dimethyltyrosine (Dmt) can increase the bioactivity of the peptide molecule [20], and the insertion of a conformationally restricted α-methylene-β-aminopropanoic acids (Map) residue into peptide molecules can lead to an improvement in the permeability of the blood-brain barrier [21].
The endogenous opioid heptapeptide VV-Hemorphin-5, known as valorphin (Val-Val-Tyr-Pro-Trp-Thr-Gln), is a part of the hemorphin family [22][23][24]. It is produced in the body by proteolytic cleavage of the region 33–39 of the β-globin chain of Hb [24][25]. Valorphin belongs to the endogenous opioid receptor agonists with a preference for the μ-opioid receptor, producing analgesia in animals [23][24]. Despite the relatively low affinity of valorphin for opioid receptors, this peptide, as with classical opioid peptides, effectively inhibits tumor cell growth [26][27]. Over the past decade, several common features have identified a family of growth-inhibitory oligopeptides. They all have a substituted N-terminus, which makes them more resistant to aminopeptidases, a very low optimally active dose (typically picomolar amounts administered in vivo and in vitro), and preferences for certain cells and tissues. This group of peptides includes valorphin, which reversibly inhibits cell proliferation, both in tumor and normal cells [27][28].
The decapeptide LVV-hemorphin-7 (Leu-Val-Val-Tyr-Pro-Trp-Thr-Gln-Arg-Phe) is the largest hemorphin found in high abundance in the mammalian nervous system. It is also the most stable and hydrophobic, in contrast to the other hemorphins [29][30][31]. The structure–activity relationship and potential antihypertensive action of LVV-hemorphins, particularly analogs of LVV-hemorphin-7, have been investigated in detail. The mechanisms by which these analogs act in cardiovascular diseases in rats have also been clarified. It is known that a number of cardiovascular changes, including blood pressure, can be activated via the sympathetic nervous system thanks to the amino acid sequence -Arg-Phe at the C-terminus of hemorphins, as well as all derivatives with a free –COOH or –CONH2 group at the C-terminus of the molecule [32]. Furthermore, LVV-hemorphin-6 and LVV-hemorphin-7 can produce anxiolytic effects by reducing anxiety in Wistar rats [33]. Recently, Hung et al. reported a positive link between alcohol-induced anti-nociception and the plasma level of LVV-hemorphin-7 [34]. These findings support the idea for further studies and efforts in developing novel analogs of LVV-hemorphin-7as potential analgesics for alcohol-induced anemia.
The Hb-derived bioactive peptides exert a modulatory role on a cannabinoid–opioid system whose mechanism underlies their implication for treating mood disorders and related behavioral changes. At the end of 2019 and the beginning of 2020, a team of scientists showed the first structural study on the binding of LVV-hemorphin-7 to ACE, IRAP, and the µ-opioid (MOR) receptor. The LVV-hemorphin-7 is a unique peptide in mammals and camels due to arginine replacing the amino acids glutamine. The results showed that camel LVV-hemorphin-7 (Leu-Val-Val-Tyr-Pro-Trp-Thr-Arg-Arg-Phe) has more stable and persistent interactions with all three receptors—MOR, ACE, and IRAP—in contrast to non-camel LVV-hemorphin-7 (Leu-Val-Val-Tyr-Pro-Trp-Thr-Gln-Arg-Phe). Further studies at the cellular and molecular level may elucidate the potential of hemorphin analogs as therapeutic agents in memory loss, hypertension, and analgesia [35][36][37].

2. Chemistry and Biology of Synthetic Hemorphin Analogs Containing Non-Natural Amino Acids

As can be seen in Figure 1, the most schematic pathway from the synthesis of a peptide to its biological tests is:
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Figure 1. An overview of the peptide pathway—from design to biological testing.
-
Design of the peptide—planning of the desired peptide compound with expected biological activity, what modifications to be made, in which part of the molecule to be made, what properties we expect to obtain, etc.
-
Choice of a reliable method used to obtain the desired peptide—peptide synthesis in solution or solid-phase peptide synthesis (SPPS). The solid-phase peptide synthesis by the Fmoc-strategy is the most widespread and acceptable method due to the number of its advantages, including reduced reaction time for creating a peptide bond; quantitative progression of condensation reactions; the easy removal of excess reagents and solvents by washing the peptidyl-resin; minimal losses when receiving the final product.
-
The synthesized peptide must be purified using chromatography (the most used is reversed-phase high-performance liquid chromatography (RP-HPLC)).
-
Followed by the complete characterization of the peptide using modern instrumental methods and techniques: spectroscopy measurements (UV-Vis; FT-IR, NMR, fluorimetry, etc.); mass spectrometry.
-
Screening tests for potential biological activity.
Changes occurring in the amino acid scaffold can lead to the preparation of new biologically active molecules with potential application in drug design and medicinal chemistry [20][32][38][39][40]. Some of the most usually used non-natural and non-proteinogenic amino acids that are introduced into peptide chains are shown in Figure 2:
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Figure 2. Some of the most used unnatural amino acids.
Natural amino acids are replaced by non-natural and unusual amino acids, D-amino acids, α-aminophosphonic acids, and their derivatives with very different purposes: obtaining a desired conformation of the peptide; obtaining the desired biological activity; increasing their resistance to enzymatic degradation; improving the stability, efficacy, bioavailability, and other essential properties of the peptides. Therefore, the proper manipulation of amino acid residues in the peptide chain, if successful, would significantly impact the future application of synthetic peptides with non-natural amino acids [32][39][40][41][42][43].
In Table 1, the most active peptide hemorphin analogs, synthesized by our research team over the last five years, are shown.
 
Table 1. Newly synthesized synthetic peptide hemorphin analogs.
№ Abbreviations Given in Articles Peptide Molecular Formula Biological Activity, Reference
    Hemorphin-4 analogs    
1 P4-1 Tyr-Ac5c-Trp-Thr-NH2 C30H38N6O6 anticonvulsant activity, [44]
2 P4-2 Tyr-Ac6c-Trp-Thr-NH2 C31H40N6O6 anticonvulsant activity, [44]
3 P4-3 Aaa-Tyr-Pro-Trp-Thr-NH2 C40H50N6O7 anticonvulsant activity, [44]
4 P4-4 Aaa-Tyr-Ac5c-Trp-Thr-NH2 C41H52N6O7 anticonvulsant activity, [44]
5 P4-5 Aaa-Tyr-Ac6c-Trp-Thr-NH2 C42H54N6O7 anticonvulsant activity, [44]
6 Dm-4 Pharmaceuticals 15 01425 i001 C36H44N8O9 anticonvulsant activity, [45]
7 Ph-4 Pharmaceuticals 15 01425 i002 C46H48N8O9 anticonvulsant activity, [45]
8 Az-H4 Pharmaceuticals 15 01425 i003 C43H47N9O7 anticonvulsant activity, [46]
9 Rh-1 rhodamineB-Gly-Tyr-Pro-Trp-Thr-NH2 C59H69N9O9 antiviral activity, [47]
10 Rh-2 rhodamineB-β-Ala-Tyr-Pro-Trp- Thr-NH2 C60H71N9O9 antiviral activity, [47]
11 Rh-3 rhodamineB-γ-Abu-Tyr-Pro-Trp-Thr-NH2 C61H73N9O9 antiviral activity, [47]
    Hemorphin-5 analogs    
12 V2/H2 Val-Val-Tyr-Pro-Trp-Thr-Dap-NH2 C42H60N10O9 antinociceptive and anticonvulsant activity, [48][49]
13 V3/H3 Val-Val-Tyr-Pro-Trp-Thr-Dab-NH2 C43H62N10O9 antinociceptive and anticonvulsant activity, [48][49]
14 V4/H4 Val-Val-Tyr-Pro-Trp-Thr-Orn-NH2 C44H64N10O9 antinociceptive and anticonvulsant activity, [48][49]
15 V5/H5 Val-Val-Tyr-Pro-Trp-Thr-Lys-NH2 C45H66N10O9 antinociceptive and anticonvulsant activity, [48][49]
16 V6/H6 Ile-Val-Val-Tyr-Pro-Trp-Thr-Gln-NH2 C50H73N11O11 antinociceptive and anticonvulsant activity, [48][49]
17 V7/H7 Aib-Val-Val-Tyr-Pro-Trp-Thr-Gln-NH2 C48H69N11O11 antinociceptive and anticonvulsant activity, [48][49]
18 V2p Pharmaceuticals 15 01425 i004 C42H60N9O12P antinociceptive and anticonvulsant activity, [50][51]
19 V3p Pharmaceuticals 15 01425 i005 C43H62N9O12P antinociceptive and anticonvulsant activity, [50][51]
20 V4p Pharmaceuticals 15 01425 i006 C47H69N10O13P antinociceptive and anticonvulsant activity, [50][51]
21 V5p Pharmaceuticals 15 01425 i007 C48H71N10O13P antinociceptive and anticonvulsant activity, [50][51]
22 V6p Pharmaceuticals 15 01425 i008 C53H80N11O14P antinociceptive and anticonvulsant activity, [50][51]
23 Dm-5 Pharmaceuticals 15 01425 i009 C51H70N12O13 anticonvulsant activity, [45]
24 Ph-5 Pharmaceuticals 15 01425 i010 C61H74N12O13 anticonvulsant activity, [45]
25 C-V Cys-Val-Val-Tyr-Pro-Trp-Thr-Glu-NH2 C47H66N10O12S antiviral and antibacterial activity, [52]
26 H-V His-Val-Val-Tyr-Pro-Trp-Thr-Glu-NH2 C50H68N12O12 antiviral and antibacterial activity, [52]
27 AC-V Aaa-Cys-Val-Val-Tyr-Pro-Trp-Thr-Glu-NH2 C58H80N10O13S antiviral and antibacterial activity, [52]
28 AH-V Aaa-His-Val-Val-Tyr-Pro-Trp-Thr-Glu-NH2 C61H82N12O13 antiviral and antibacterial activity, [52]
    Hemorphin-7 analogs    
29 2 Val-Val-Tyr-Ac5c-Trp-Thr-Gln-Arg-Phe-NH2 C60H85N15O12 anticonvulsant activity, [53]
30 3 Val-Val-Tyr-Ac6c-Trp-Thr-Gln-Arg-Phe-NH2 C61H87N15O12 anticonvulsant activity, [53]
31 4 Val-Val-Tyr-Pro-Trp-Thr-Dap-Arg-Phe-NH2 C57H81N15O11 anticonvulsant activity, [53]
32 5 Val-Val-Tyr-Pro-Trp-Thr-Dab-Arg-Phe-NH2 C58H83N15O11 anticonvulsant activity, [53]
33 6 Val-Val-Tyr-Ac5c-Trp-Thr-Dap-Arg-Phe-NH2 C58H83N15O11 anticonvulsant activity, [53]
34 7 Val-Val-Tyr-Ac5c-Trp-Thr-Dab-Arg-Phe-NH2 C59H85N15O11 anticonvulsant activity, [53]
35 8 Val-Val-Tyr-Ac6c-Trp-Thr-Dap-Arg-Phe-NH2 C59H85N15O11 anticonvulsant activity, [53]
36 9 Val-Val-Tyr-Ac6c-Trp-Thr-Dab-Arg-Phe-NH2 C60H87N15O11 anticonvulsant activity, [53]
37 H7-1 Ile-Val-Val-Tyr-Pro-Trp-Thr-Gln-Arg-D-Phe-NH2 C65H94N16O13 anticonvulsant activity, [54]
38 H7-2 Ile-Val-Tyr-Pro-Trp-Thr-Gln-Arg-D-Phe-NH2 C60H85N15O12 anticonvulsant activity, [54]
39 H7-3 D-Leu-Val-Val-Tyr-Pro-Trp-Thr-Gln-Arg-D-Phe-NH2 C65H94N16O13 anticonvulsant activity, [54]
40 H7-4 D-Val-Val-Tyr-Pro-Trp-Thr-Gln-Arg-D-Phe-NH2 C59H83N15O12 anticonvulsant activity, [54]
41 H7-5 Pharmaceuticals 15 01425 i011 C68H101N16O16P anticonvulsant activity, [54]
42 H7-6 Pharmaceuticals 15 01425 i012 C68H101N16O16P anticonvulsant activity, [54]
43 H7-7 Pharmaceuticals 15 01425 i013 C62H90N15O15P anticonvulsant activity, [54]
44 H7-8 Pharmaceuticals 15 01425 i014 C62H90N15O15P anticonvulsant activity, [54]
45 Dm-7 Pharmaceuticals 15 01425 i015 C72H102N18O16 anticonvulsant activity, [45]
46 Ph-7 Pharmaceuticals 15 01425 i016 C82H106N18O16 anticonvulsant activity, [45]
47 RGD1 Val-Val-Tyr-Pro-Trp-Thr-Gln-Arg-Phe-Arg-Gly-Asp-NH2 C71H103N21O17 antinociceptive activity, [55]
48 RGD2 Asp-Gly-Arg-Val-Val-Tyr-Pro-Trp-Thr-Gln-Arg-Phe-Arg-Gly-Asp-NH2 C83H123N27O22 antinociceptive activity, [55]
49 NH7C Nic-Leu-Val-Val-Tyr-Pro-Trp-Thr-Glu-Arg-Phe-Cys-NH2 C74H101N17O16S antiviral and antibacterial activity, [52]
50 NCH7 Nic-Cys-Leu-Val-Val-Tyr-Pro-Trp-Thr-Glu-Arg-Phe-NH2 C74H101N17O16S antiviral and antibacterial activity, [52]
The structure–activity relationship of a series of new analogs of the shortest of all hemorphins, hemorphin-4, was elucidated by Todorov et al. (compounds P4-1, P4-2, P4-3, P4-4, and P4-5) [44]. Modifications have been made by replacing Pro at position 2 with the unnatural and conformationally restricted amino acids Ac5c and Ac6c, as well as introducing the adamantane residue from the N-terminus of the hemorphin-4 molecule that would lead to multiple target systems. The most potent anticonvulsant activity has been exhibited by the peptide analog P4-5, which contains an adamantane residue at the N-terminus and a cyclohexane ring at position 2 (Figure 3). The peptide analog P4-5 had the lowest ED50 among other hemorphin-4 peptide analogs and the protective index (PI) with an appropriate safety margin in the MES test (Table 2) that proves the efficacy of active agents against partial and generalized seizure-type epilepsy [56]. In addition, the P4-5 analog exhibited higher potency in the MES test than in the referent angiotensin (Ang) IV [44]. Furthermore, the structure–activity relationship analysis suggests that the presence of an adamantane residue at the N-terminus seems crucial for the anticonvulsant activity in the MES test, and, therefore, against the seizure spread. Interestingly, the expressed biological activity of P4-5 is likely due to an appropriate conformational fit of the peptide to the insulin-regulated aminopeptidase (IRAP) receptor and the great lipophilicity and hydrophobicity of the molecule [44]. It is known that hemorphins and Ang IV could bind to the receptor system (IRAP) and share a common metabolic pathway [30]. Recently, it has been reported that both P4-4 and P4-5 peptide analogs are positively charged based on their pKa constants and the isoelectric points at pH 7.4 [44]. In the 6 Hz test, considered a model of drug-resistant epilepsy [57], the P4-5 peptide analog exerted an effect comparable to those of the other two peptide analogs as follows: P4-1: ED50 = 0.52; P 4-4: ED50 = 0.44; P4-5: ED50 = 0.64 mg/kg (Table 3). It is suggested that sodium channels are the targets of drugs with activity against 6 Hz psychomotor seizures [58]. The P4-4 and P4-5 peptide analogs demonstrated the lowest seizure threshold for intravenous pentylenetetrazol (ivPTZ)-induced clonic seizures (Table 4). It is suggested that drugs with potency against the clonic phase in this test might affect the GABAA receptor complex and GABA-ergic neurotransmission [59].
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Figure 3. Chemical structure of peptide analog P4-5.
 
Table 2. Quantitative assessment of anticonvulsant activity of hemorphin peptides in the MES test in mice.
Drug TPE a ED50 b µg 95% Confidence Interval TD50 c PI d
(min)
Phenytoin 60 4.92 mg.kg−1 (2.57–9.39) >100 mg.kg−1 >20.35
Hemorphin-4 analogs 10        
P4-1   - - - -
P4-2   2.33 (1.13–4.83) >10 >4.29
P4-3   1.66 (1.24–2.24) >10 >6.02
P4-4   2.33 (1.13–4.83) >10 >4.29
P4-5   0.41 (0.19–0.90) >10 >24.39
Peptide-based chemosensor bearing azobenzene side chain bio photoswitch 10        
Cis Az-H4   1.71 (1.16–2.51) >10 >5.85
Trans A-H4   1.51 (1.04–2.02) >10 >6.62
VV-Hemorphin-5 analogs 10        
V2   - - - -
V3   - - - -
V4   3.63 (2.45–5.38) >20 >5.51
V5   3.19 (2.62–3.87) >20 >6.27
V6   16.77 (11.08–25.36) >20 >1.19
V7   16.55 (12.78–21.41) >20 >1.21
5,5-dimethyl- and 5,5-diphenylhydantoin-conjugated hemorphin derivatives 10        
Dm-4   0.36 (0.13–1.0) >3 >8.33
Dm-5   0.74 (0.06–8.8) >5 >6.76
Dm-7   0.7 (0.05–9.58) >10 >14.29
Ph-4   0.56 (0.06–5.34) >8 >14.29
Ph-5   0.25 (0.10–0.60) >5 >20
LVV- and VV-hemorphin-7 analogs 10        
H7-1   - - - -
H7-2   0.94 (0.36–2.47) >8 >8.51
H7-3   0.68 (0.19–2.51) >8 >11.76
H7-4   2.54 (1.38–4.64) >15 >5.91
H7-5   1.53 (0.60–3.88) >3 >1.96
H7-6   0.38 (0.13–1.15) >3 >7.89
H7-7   1.58 (0.68–3.70) >5 >3.16
H7-8   1.67 (1.11–2.51) >7 >4.19
 
Table 3. Quantitative assessment of anticonvulsant activity of hemorphin peptides in the 6 Hz test in mice.
Drug TPE a ED50 b 95% Confidence Interval TD50 c PI d
(min) µg
Hemorphin-4 analogs 10        
P4-1   0.52 (0.33–0.82) >5 >9.62
P4-2   2.16 (1.87–2.49) >5 >2.31
P4-3   0.83 (0.57–1.19) >5 >6.02
P4-4   0.44 (0.25–0.78) >5 >11.36
P4-5   0.64 (0.40–1.02) >5 >7.81
VV-Hemorphin-5 analogs 10        
V2   9.97 (9.07−10.90) >20 2
V4   5.09 (4.31–6.02) >20 3.93
V5   9.89 (8.64–11.34) >20 2.02
V6   5.55 (5.51–5.58) >20 7.84
V7   6.61 (6.59–6.62) >20 3.03
N-modified analogs of VV-hemorphin-5 with aminophosphonate moiety 10        
V2p          
V3p   6.47 (3.96–10.57) >20 3.09
V4p   4.31 (2.76–10.47) >20 4.64
V5p   12.55 (9.26–16.99) >30 2.39
V6p   14.11 (9.17 –21.47) >40 2.83
5,5-dimethyl- and 5,5-diphenylhydantoin-conjugated hemorphin derivatives 10        
Dm-4   0.53 (0.38–0.73) >5 9.43
Dm-5   0.64 (0.40–1.01) >5 7.81
Dm-7   0.54 (0.26–1.11) >5 9.26
Ph-4   0.22 (0.13–0.37) >5 22.72
Ph-5   0.27 (0.11–0.69) >5 18.52
Ph-7   0.23 (0.10–0.52) >5 21.74
VV Hemorphin-7 analogs containing unnatural amino acids 10        
VV-H-2   5.69 (3.67–8.81) >30 >5.27
VV-H-3   5.69 (3.67–8.81) >30 >5.27
VV-H-4   3.83 (1.50–9.76) >20 >5.22
VV-H-5   0.89 (0.54–1.46) >20 >22.47
VV-H-6   2.67 (4.67–8.19) >20 >7.49
VV-H-7   0.89 (0.66–2.00) >20 >22.47
VV-H-8   1.01 (0.29–3.55) >20 >19.80
VV-H-9   1.09 (0.40–3.00) >30 >27.52
LVV- and VV-hemorphin-7 analogs 10        
H7-1   0.33 (0.32–0.33) >5 >15.15
H7-2   2.6 (1.58–4.55) >5 >1.87
H7-3   - - - -
H7-4   - - - -
H7-5   2.16 (1.70–2.74) >5 >2.31
H7-6   2.44 (1.41–4.21) >5 >2.05
H7-7   2.16 (1.70–2.74) >5 >2.31
H7-8   3.03 (2.44–3.74) >5 >1.65
 
Table 4. Analysis of the anticonvulsant activity of hemorphin peptides in ivPTZ seizure test in mice.
Drug TPE a Comparison of Activity Related to the Threshold Dose (µg/10 µL) for Clonic Seizures
(min)
Hemorphin-4 analogs 10  
P4    
P4-2   P4-4 = P4-5 > P4-2 = P4-3 > P4
P4-3    
P4-4    
P4-5    
VV-Hemorphin-5 analogs 10  
V1    
V2   V1 = V4 > V2
V4    
V5    
V6    
V7    
N-modified analogs of VV-hemorphin-5 with aminophosphonate moiety 10 V1 = V3p
V1    
V2p    
V3p    
V4p    
V5p    
V6p    
Hemorphin-7 analogs containing unnatural amino acids 10 VV–H7 = V–H4
VV-H7    
VV-H-2    
VV-H-3    
VV-H-4    
VV-H-5    
VV-H-6    
VV-H-7    
VV-H-8    
VV-H-9    
LVV- and VV-hemorphin-7 analogs 10  
H7   H7-5> H7 = H7-3 = H7-6 = H7-7 = H7-8 > H7-1
H7-1    
H7-2    
H7-3    
H7-4    
H7-5    
H7-6    
H7-7    
H7-8
The Tyr-Pro-Trp fragment is involved in the modulation of numerous biological processes through the activation of opioid receptors [22] and, thus, participates in [38][60]. In addition, the adamantane and cycloalkyl groups provide the desired membrane permeability and conformational fit in the intercellular space enabling efficient transport across lipid membranes [58][61]. Adamantane-based compounds are widely used in practice as potential agents for treating neurological and antiviral conditions, malaria, type 2 diabetes, and inflammatory conditions [62][63]. Some modified adamantane compounds have been reported to show anticonvulsant activity in animal models. In addition to its anticonvulsant properties, the adamantane residue can also act as an analgesic in mouse models [64][65].
In the last year, Todorov’s group [47][52] showed the promising antiviral and antibacterial activity of some new N- and C-modified hemorphin analogs containing different amino acids (Cys, Glu, and His), 1-adamantane carboxylic acid, and niacin against the human respiratory syncytial virus (HRSV-S2) and human adenovirus serotype 5 (HAdV-5) and against B. cereus and P. Aeruginosa (compounds C-V, H-V, AC-V, AH-V NH7C, and NCH7) [47]. The authors were the first to investigate the structural-textile application and potential antimicrobial activities of both hemorphin derivatives and hemorphin-treated textile material [47][52].
The insertion of chromophoric groups that possess interesting features into peptides for photodynamic control of peptide biomolecules has been investigated intensively in recent years [66][67][68]. The influence of cis(Z)- and trans(E)- isomers of recently synthesized biopeptide-bearing azobenzene on the N-side chain of hemorphin-4 has been studied (compound AzP) [46]. Moreover, some researchers have synthesized, characterized, and investigated the structure-related properties of new rhodamineB-conjugated hemorphin-4 analogs as potentially sensitive fluorescent probes (compounds № 9–11). These hybrid peptides contain different aliphatic amino acid residues between the chromophoric group, rhodamine B to the N-side, and the amino acid scaffold of natural hemorphin-4 [47].
The idea of introducing non-proteinogenic and natural amino acids for the synthesis of new analogs of VV-hemorphin-5 modified from the C- and N-termini (compounds № 12–17) has been successfully carried out by Todorov et al. [48][49], obtaining peptide structures with the sequences: Xxx-Val-Val-Tyr-Pro-Trp-Thr-Gln-NH2 and Val-Val-Tyr-Pro-Trp-Thr-Yyy-NH2, where Xxx is Ile or Aib (α-aminoisobutyric acid) and Yyy are Lys/Orn/Dap (2,3-diaminopropanoic acid)/Dab (2,4-diaminobutanoic acid) (see Figure 4). All of these new peptide molecules have been tested for anticonvulsant and potential antinociceptive activities in mice, with the derivative H2 (Val-Val-Tyr-Pro-Trp-Thr-Dap-NH2) showing the highest biological activity, in whose structure glutamine is replaced with Dap. In comparison, the derivative V4 (Val-Val-Tyr-Pro-Trp-Thr-Orn-NH2), containing a non-proteinogenic amino acid Orn at the C-terminal, showed pronounced anticonvulsant activity, comparable to that of natural valorphin (Table 2, Table 3 and Table 4) [48][49]. None of the newly synthesized analogs of VV-Hemorphin-5 affected motor coordination. While V4 and V5 analogs had similar ED values in the MES test (V4: ED50 = 3.63 and V5: ED50 = 3.19), V4 exhibited an activity comparable to that of V6 against the 6 Hz psychomotor seizures (V4: ED50 = 5.09 and V6: ED50 = 5.55) (Table 2 and Table 3). The in silico analysis suggested that changes in Position 7 (replacement of Gln by Lys) must be the crucial factor responsible for the anticonvulsant activity of V5 against generalized seizures in the MES test and activated opioid δ receptors [67]. On the other hand, this activation might be associated with the insertion of Ile at Position 1 in the V6 activity against psychomotor seizures.
Pharmaceuticals 15 01425 g004 550
Figure 4. Chemical structure of H2 and V4 peptide analogs.
Moreover, the V4 peptide increased the threshold for clonic seizures induced by ivPTZ in the lowest dose of 5 µg, comparable to the positive control. The universal potency demonstrated by V4 in three seizure tests with a different mechanism of action might be due to the insertion of amino acid Orn at Position 7 of VV-5 predisposed to various targets. Therefore, the position of replacement and the nature of the inserted group in recently synthesized VV-Hemorphin-5 analogs containing nonproteinogenic and natural amino acids seem critical factors in determining the anticonvulsant and antinociceptive activity of the associated receptor binding.
An active valorphin analog was obtained as a potent inhibitor of dipeptidyl peptidase III by intermolecular C–H arylation on the resin between Trp at position 5 and Tyr at position 3 by using solid-phase peptide synthesis. This peptide is structurally close to spinorphin (Leu-Val-Val-Tyr-Pro-Trp-Thr), an endogenous peptide with antinociceptive action [69][70][71].

For the first time, α-aminophosphonic acids have been introduced into hemorphin peptides (compounds № 18–22 and 41–44) [50][51]. α-Aminophosphonates and aminophosphonic acids occupy an essential place among compounds containing a P-C bond and an amino group. They are structural analogs of natural α-amino acids, which are the “building blocks” of peptides and proteins. Their structure is of interest due to their diverse biological role. The obtained N-modified analogs of VV-hemorphin-5 containing an aminophosphonic residue have been described in detail in terms of structure-activity and have been investigated for antinociceptive and anticonvulsant activity. In the literature, it has been reported that the most potent hemorphin derivative was the V3p, with the lowest ED50 of 4.31 µg against psychomotor seizures and ivPTZ clonic seizures (Tables 3 and 4) [50]. The results of the docking study of the obtained in vivo results suggest that binding to the k-opioid receptor is the most likely mechanism of action of the peptide derivatives with anticonvulsant activity. These data lead us to hypothesize that modification of the two N-terminal Val in the peptide molecules with an aminophosphonate residue in phosphopeptide analogs leads to significant changes in peptide activity and affinity [50][51].

For the first time, C-5-substituted hydantoins were introduced into hemorphins, aiming for a synergistic effect to enhance anticonvulsant activity (compounds № 6, 7, 23, 24, 45, and 46) [45]. Of these hybrid structures, the strongest anticonvulsant activity was reported for VV-hemorphin-5, possessing a 5,5′-diphenylhydantoin residue at the N-terminus and a hydrophobic Val–Val–Tyr–Pro–Trp–Thr–Gln–CONH2 amino acid sequence of the peptide molecule (Ph5). This compound showed low ED50 for MES and the 6 Hz test, respectively, compared to other tested peptide analogs (Tables 2 and 3). In silico analysis suggests that the underlying mechanism of the anticonvulsant effect of Ph-5 involves blocking sodium channels [45].

A series of Phe-modified analogs of hemorphin-7-NH2 were synthesized and characterized by replacing Phe at position 7 with various natural and unnatural amino acids: Leu, MePhe, D-Phe, Tic, Trp, Met, Oic, Phg (phenylglycine), pNO2Phe, Nle (norleucine), pClPhe, Thi, and Cha. Of all synthetic analogs, the most active are those containing unnatural amino acids: tetrahydro-isoquinoline-3-carboxylic acid (Tic), pClPhe, 3-thienylalanine (Thi), octahydroindole-2-carboxylic acid (Oic), and 3-cyclohexylalanine (Cha). Using phenytoin (5,5′-diphenylhydantoin) as a sodium channel blocker, it has been hypothesized that LVV-hemorphin-7 analogs activate the sympathetic nervous system via interaction with specific receptors functionally linked to phenytoin-sensitive sodium channels. Substitution of Arg at position 6 with Lys slightly reduced blood pressure, in contrast to its substitution with the amino acids citrulline, D-Arg, NO2Arg, Orn, or Ala, where it was significant [28]. Conversion of the C-terminal –COOH group with its amide –CONH2 in this type of compound significantly increased the activity of the corresponding peptide analog, indicating that the C-terminal –COOH group is not essential for activity. One possible reason for this is that such a change in the molecule leads to an increase in the resistance of the peptide to enzymatic degradation by endogenous carboxypeptidases [28][36][37]. Using proteomic studies, the biological role of LVV- and VV-hemorphin-7 as potential biomarkers in patients with posterior cranial fossa brain tumors has been demonstrated. It has been found that the presence of these two hemorphins can be used in the clinical diagnosis of this disease. In the presence of a brain tumor, both hemorphins are not detected in cerebrospinal fluid (CSF) analysis. At the same time, in the case of postoperative removal, they are present [72][73]. 

Two new N- and C-modified analogs of VV-hemorphin-7 containing RGD (Arg–Gly–Asp) residues as potential nociceptive agents and bioactive materials have been elucidated in detail № 47 and 48) [55]. From the eight LVV- and VV-hemorphin-7 analogs (compounds № 37–44), the H7-1 peptide analog showed the highest potency against the 6 Hz psychomotor seizures with ED50 of 0.33 µg (Table 3). However, while the H7-6 had the lowest ED50 in the MES test (Table 4), the H7-5 peptide analog raised the ivPTZ-induced clonic seizure at the highest rate at the doses used among the eight synthetized LVV- and VV-hemorphin-7 analogs (Table 4) [54]. Therefore, the modification at the N- and C-terminus with certain amino acids seems to play a critical role in the design of new LVV- and VVhemorphin-7 analogs.

Todorov et al. have synthesized and characterized a series of new analogs of VV-hemorphin-7 (compounds № 29-36) with potential anticonvulsant activity, modified with unnatural amino acids, following the structure Val-Val-Tyr-Xxx-Trp-Thr-Yyy-Arg-Phe-NH2, where Xxx is Ac5c (1-aminocyclopentane carboxylic acid) or Ac6c (1-aminocyclohexanecarboxylic acid) and Yyy is Dap (2,3-diaminopropane acid) or Dab (2,4-diaminobutanoic acid) [53]. The peptide analog VV-H5, containing diaminobutanoic acid in its molecule, showed the highest anticonvulsant activity. Moreover, this peptide analog had the lowest ED50 of 0.89 µg against psychomotor seizures and ED50 of 0.38 µg against the MES among the eight novel compounds (Tables 2 and 3). In addition, this peptide analog increased the threshold for ivPTZ clonic seizures at the lowest dose of 5 µg injected (Table 4). Interestingly, VV-H5 differs from VV-H4 by only one -CH2 group in the molecule, which is crucial for the anticonvulsant activity of this hemorphin derivative.

Analytical Characteristics of Hemorphin Analogs

It is known that some identical amino acid residues can have different reactivity with respect to given chemical reagents. For example, in an enzyme molecule, only one or a small number of side chains of amino acid residues located in the "active" center can bind substrates or coenzymes, while others with the same chemical composition cannot. As is known, a large part of the hydrophobic side chains are located in the interior of the molecule, thus building a compact core, while the polar and electron-charged groups are supported on the surface of this matrix. Moreover, the physical and chemical properties of the functional groups are strongly influenced by the nature of the microenvironment. Peptides exhibit partial solubility in aqueous (phosphate buffer, pH 6.86±0.01) and (organic) environments, with varying degrees of hydrophilicity and hydrophobicity (Figure 5). Ph-4 and Dm-4 show the greatest hydrophobicity, and Dm-5 and Ph-5 show the greatest tendency to dissolve in organic media. This is due to the fact that the attachment of a non-water-soluble hydantoin component to the main short-chain peptide scaffold stabilizes the zwitterionic form in solutions with a pH of about 7 and interferes with solubility in aqueous solutions. For these compounds, the isoelectric points are around 7.0. рI values close to and around 7 are observed for most short-chain peptide modifications (Figure 6). Compounds P4-4 and P4-5 with modifications Ac5c, Ac6c have pI values around 7, and it is the zwitterionic form in which they will be at this pH that will interfere with their solubility when preparing, for example, injection solutions for biological analyses. Peptide forms with these modifications also showed the least pronounced biological activities. As an important parameter evaluating the behavior of non-peptides in solution are also acid-base constants. Determination of the equilibrium constants (pK) of proton dissociation from ionizable side chains of amino acids represents a very important application of spectroscopy and electrochemistry in peptide chemistry. This definition allows conclusions to be drawn regarding the location of these groups in the peptide matrix, as well as their involvement in various interactions. As mentioned the amino acid fragment of the hemorphin molecule: Tyr-Pro-Trp is the main sequence thanks to which receptor binding takes place. On the other hand, the amino acids tyrosine and tryptophan, bonded in a peptide chain, are one of the main amino acids exhibiting fluorescent, electrochemical and acid-basic properties. Table 5 gives the determined pK values of the hemorphin peptides, calculated by applying different analytical techniques, most often by potentiometric titration or mathematical processing of data from the fluorescence/voltammetric analysis. Hemorphine derivatives have acidic properties, which turn them into protolytes of different strengths depending on the amino acid radicals: the more acidic amino acids in the peptide, the stronger its acidic properties are expressed. Regardless of the peptide modifications made, the determined acidity constants refer to the side P-groups of tyrosine, the indole nucleus of tryptophan, and arginine in the arginine-containing peptides, exhibiting different degrees of polarity at a pH close to the physiological values of 6-8 (corresponding to the conditions of the cell cytosol). Most peptide derivatives showed approximate pK values related to proton exchange with the -OH group of tyrosine and the indole moiety of tryptophan. As can be seen, peptide derivatives containing a phosphonic group adjacent to the amino acid tyrosine (V2P-V3P series) have weaker protolytic properties, and the protolytic power of long-chain hemorphin derivatives increases with the distance of the -OH group of tyrosine from the corresponding structural modification.

Table 5. Parameters of the voltammetric measurements and the electrochemical data of peptides.

Peptide

pKa1; pKa2 Constants

 

 

 

P4

by potentiometric titration

3.80; 6.44, [44]

P4-1

3.89; 6.52, [44]

P4-2

3.93; 6.71, [44]

P4-3

3.88; 6.93, [44]

P4-4

6.16; 8.90, [44]

P4-5

6.20; 9.06, [44]

Dm-4

by potentiometric titration

2.86; [44]

Ph-4

by potentiometric titration

2.98; [45]

Rh-1

by potentiometric titration

2.81; 6.60, [47]

Rh-2

2.78;6.38, [47]

Rh-3

2.86;6.39, [47]

Hemorphin-5 analogs

V2/H2

by potentiometric titration

9.23, [48][49]

V3/H3

8.12, [48][49]

V4/H4

7.83, [48][49]

V5/H5

8.24, [48][49]

V6/H6

8.01, [48][49]

V7/H7

8.17, [48][49]

V2p

by potentiometric titration and voltamperometry

8.93, [50][51]

V3p

8.83, [50][51]

V4p

7.92, [50][51]

V5p

8.97, [50][51]

V6p

9.05, [50][51]

Dm-5

by potentiometric titration

3.06; 7.14, [45]

Ph-5

3.09; 6.98, [45]

C-V

by fluorimetry

5.18, [52]

H-V

4.75, [52]

AC-V

5.43, [52]

AH-V

4.84, [52]

Hemorphin-7 analogs

2

by potentiometric titration

8.04(Val); 5.34(Tyr), [53]

3

7.49(Val); 4.83(Tyr), [53]

4

7.10(Val);5.46(Dap, Dab); 3.14(Tyr), [53]

5

8.08(Val);7.21(Dap, Dab); 5.98(Tyr),[53]

6

8.15(Val);6.87(Dap, Dab); 4.72(Tyr), [53]

7

8.21(Val);7.26(Dap, Dab); 4.70(Tyr), [53]

8

9.20(Val);8.03(Dap, Dab); 5.27(Tyr), [53]

9

9.08(Val);8.80(Dap, Dab); 4.66(Tyr), [53]

H7-1

by potentiometric titration

2.98; 6.12, [54]

H7-2

3.09; 6.62, [54]

H7-3

3.05; 6.78, [54]

H7-4

3.22; 6.52, [54]

H7-5

3.17; 6.23, [54]

H7-6

2.98; 5.85, [54]

H7-7

3.15; 6.09, [54]

H7-8

2.78; 5.52, [54]

Dm-7

by potentiometric titration

3.19; 5.11, [45]

Ph-7

3.23; 6.45, [45]

RGD1

by potentiometric titration

3.53; 6.42, [55]

RGD2

3.48; 6.34, [55]

NH7C

by fluorimetry

5.07, [52]

NCH7

4.78, [52]

 

Figure 5. Logarithmic values of the partition coefficient (log P) of some of the investigated hemorphin compounds.

Figure 6. Summary plot of isoelectric point (pI) values of hemorphin analogs.

 

Electrochemical behavior of hemorphin analogs

A comparative review of the electrochemical properties of peptide derivatives would be of interest from a scientific point of view, as the method offers the elucidation of basic mechanisms of action and the detection of molecular and structural modifications (aggregation). Electrochemical methods add a fresh, new perspective to the research field of hemorphin analogs in terms of their rapid detection, characterization, the study of redox behavior, and electrode response nature. Most of the studied hemorphin derivatives contain only the voltammetrically active tyrosine and tryptophan, connected in the sequence -Tyr-Pro-Trp- and their oxidation occurs thanks to the presence of p-electrons at the hydroxyl group of the phenol part (Tyr) and indole ring (Trp), respectively [48][49][50]. Studies were carried out in different electrolyte environments by using differently charged surfaces (Table 6). On a glass carbon electrode, at pH⁓7, the oxidation of hemorphin analogs is irreversible, which occurs at positive potentials (Ep⁓+0.4V for Vp series and Ep⁓+0.7 for H7 series V vs. Ag/AgCl), corresponding to the signal of tyrosine due to –OH group of the phenol part which is oxidized to a glass carbonic electrode at potential closed to +0.7[74]. The oxidation of histidine and cysteine to peptides containing them at a glassy carbon electrode is an irreversible, diffusion-controlled, and pH-dependent process (Table 6) that occurs at Ep ⁓ 1.2 V, vs. Ag/AgCl[75]. A medium of tetrabutylammonium persulfate with methanol proved to be favorable for the detection and determination of hemorphin analogs at mercury electrodes, with the resulting well-shaped reduction/oxidation peaks indicating reversible to quasi-reversible electrode processes. Analyzes showed that the reactivity of the tyrosine and tryptophan regions was conserved. This, together with the fact that the concentration dependence of the current signal is proportional, gives us reason to conclude that in these environments the structure of the compounds is preserved and aggregation does not occur regardless of the modification of the molecule. Electrochemical methods of investigating the aggregation and fibrillization of hemorphin peptides could become important additional tools in biochemical research, leading to new insights into the molecular mechanisms underlying pathogenesis.

Table 6. Parameters of the voltammetric measurements and the electrochemical data of peptides [45][46][48][49][50][51][52][53][54][55].

3. Conclusions

Our review showed that more than 50 new hemorphin analogs obtained by solid-phase peptide synthesis by the Fmoc-strategy have been synthesized and characterized up to date. These hemorphin peptides contain various unnatural and unusual amino acids, D-amino acids, α-aminophosphonic acids, and their derivatives that are mentioned in this article. Structure-activity relationship studies show that not only the position of the modification, but also the nature of the amino acid involved leads to significant changes in the physicochemical properties (change in pKa, pI, and logP of the peptide), biological activity, and receptor affinity. It can be summarized that even the smallest change in the hemorphin molecule has a great influence on the biological activity, such as the introduction of the unnatural amino acid Dap, and the replacement of Pro with the conformationally constrained amino acids (Ac5c, Ac6c, and adamantane moieties). Structure-activity analysis revealed that the incorporation of an adamantane residue at the N-terminus is necessary for protection against the spread of seizures. Data obtained so far have shown that modification of the two N-terminal Vals in peptide molecules by an aminophosphonate residue in phosphopeptide analogs requires increased biological activity and receptor affinity, from which it can be concluded that the successful design of new analogs of LVV- and VV-hemorphin-7 involves modification of the N- and C-termini with specific amino acids. Predictions from the docking analysis suggest that binding to the k-opioid receptor is the most relevant mechanism of action for the new peptide analogs that possess unnatural amino acids. All hemorphin analogs can be successfully detected at low concentrations by applying voltammetric techniques on solid and mercury electrodes. Electrochemical methods are a good alternative for proving molecular conformational changes and processes of aggregation and peptide fibrillization and can be applied in studying the properties of hemorphin peptides in environments with different matrix compositions.

 

Funding: This work was financially supported by the Bulgarian National Scientific Fund projects KП-06-ДK1/11 and КП-06-ДО-02/3 of the Ministry of Education and Science, Bulgaria.

This entry is adapted from the peer-reviewed paper 10.3390/ph15111425

References

  1. Mielczarek, P.; Hartman, K.; Drabik, A.; Hung, H.-Y.; Huang, E.Y.-K.; Gibula-Tarlowska, E.; Kotlinska, J.H.; Silberring, J. Hemorphins—From Discovery to Functions and Pharmacology. Molecules 2021, 26, 3879.
  2. Fukui, K.; Shiomi, H.; Takagi, H.; Hayashi, K.; Kiso, Y.; Kitagawa, K. Isolation from bovine brain of a novel analgesic pentapeptide, neo-kyotorphin, containing the Tyr-Arg (kyotorphin)unit. Neuropharmacology 1983, 22, 191–196.
  3. Schechter, A.N. Hemoglobin research and the origins of molecular medicine. Blood J. Am. Soc. Hematol. 2008, 112, 3927–3938.
  4. Liu, L.; Zeng, M.; Stamler, J.S. Hemoglobin induction in mouse macrophages. Proc. Natl. Acad. Sci. USA 1999, 96, 6643–6647.
  5. Newton, D.A.; Rao, K.M.K.; Dluhy, R.A.; Baatz, J.E. Hemoglobin is expressed by alveolar epithelial cells. J. Biol. Chem. 2006, 281, 5668–5676.
  6. Wride, M.A.; Mansergh, F.C.; Adams, S.; Everitt, R.; Minnema, S.E.; Rancourt, D.E.; Evans, M.J. Expression profiling and gene discovery in the mouse lens. Mol. Vis. 2003, 9, 360–396.
  7. Setton-Avruj, C.P.; Musolino, P.L.; Salis, C.; Allo, M.; Bizzozero, O.; Villar, M.J.; Pasquini, J.M. Presence of α-globin mRNA and migration of bone marrow cells after sciatic nerve injury suggests their participation in the degeneration/regeneration process. Exp. Neurol. 2007, 203, 568–578.
  8. Ohyagi, Y.; Yamada, T.; Goto, I. Hemoglobin as a novel protein developmentally regulated in neurons. Brain Res. 1994, 635, 323–327.
  9. Schelshorn, D.W.; Schneider, A.; Kuschinsky, W.; Weber, D.; Krüger, C.; Dittgen, T.; Maurer, M.H. Expression of hemoglobin in rodent neurons. J. Cereb. Blood Flow Metab. 2009, 29, 585–595.
  10. Richter, F.; Meurers, B.H.; Zhu, C.; Medvedeva, V.P.; Chesselet, M.F. Neurons express hemoglobin α-and β-chains in rat and human brains. J. Comp. Neurol. 2009, 515, 538–547.
  11. Ivanov, V.T.; Karelin, A.A.; Philippova, M.M.; Nazimov, I.V.; Pletnev, V.Z. Hemoglobin as a source of endogenous bioactive peptides: The concept of tissue-specific peptide pool. Pept. Sci. 1997, 43, 171–188.
  12. Karelin, A.A.; Blishchenko, E.Y.; Ivanov, V.T. Fragments of Functional Proteins: Role in Endocrine Regulation. Neurochem. Res. 1999, 24, 1117–1124.
  13. Giardina, B. Hemoglobin: Multiple molecular interactions and multiple functions. An example of energy optimization and global molecular organization. Mol. Asp. Med. 2022, 84, 101040.
  14. Amanat, A.; Alzeyoudi, C.A.; Almutawa, A.C.; Alnajjar, A.H.; Vijayan, R. Molecular basis of the therapeutic properties of hemorphins, Pharmacol. Res. 2020, 158, 104855.
  15. Yoshikawa, M. Bioactive peptides derived from natural proteins with respect to diversity of their receptors and physiological effects. Peptides 2015, 72, 208–225.
  16. Brantl, V.; Gramsch, C.; Lottspeich, F.; Mertz, R.; Jaeger, K.H.; Herz, A. Novel opioid peptides derived from hemoglobin: Hemorphins. Eur. J. Pharmacol. 1986, 125, 309–310.
  17. Yang, Y.R.; Chiu, T.H.; Chen, C.L. Structure–activity relationships of naturally occurring and synthetic opioid tetrapeptides acting on locus coeruleus neurons. Eur. J. Pharmacol. 1999, 372, 229–236.
  18. Mollica, A.; Pinnen, F.; Stefanucci, A.; Mannina, L.; Sobolev, A.P.; Lucente, G.; Davis, P.; Lai, J.; Ma, S.-W.; Porreca, F.; et al. cis-4-Amino-l-proline Residue as a Scaffold for the Synthesis of Cyclic and Linear Endomorphin-2 Analogues: Part 2. J. Med. Chem. 2012, 55, 19–8477.
  19. Mollica, A.; Stefanucci, A.; Costante, R.; Novellino, E. Pyroglutamic Acid Derivatives: Building Blocks for Drug Discovery. HETEROCYCLES 2014, 89, 1801.
  20. Mollica, A.; Stefanucci, A.; Costante, R.; Hruby, V.J. Chapter 2—Rational Approach to the Design of Bioactive Peptidomimetics: Recent Developments in Opioid Agonist Peptides. Stud. Nat. Prod. Chem. 2015, 46, 27–68.
  21. Schiller, P.W. Development of opioid peptide analogs as pharmacologic tools and as potential drugs: Current status and future directions. NIDA Res. Monogr. 1991, 112, 180–197.
  22. Blishchenko, E.Y.; Sazonova, O.V.; Kalinina, O.A.; Yatskin, O.N.; Philippova, M.M.; Surovoy, A.Y.; Karelin, A.A.; Ivanov, V.T. Family of hemorphins: Co-relations between amino acid sequences and effects in cell cultures. Peptides 2002, 23, 903–910.
  23. Maurer, R.; Römer, D.; Büscher, H.H.; Gähwiler, B.H.; Thies, P.W.; David, S. Valorphin: A novel chemical structure with opioid activity. Neuropeptides 1985, 5, 387–390.
  24. Erchegyi, J.; Kastin, A.J.; Zadina, J.E.; Qiu, X.D. Isolation of a heptapeptide Val-Val-Tyr-Pro- Trp-Thr-Gln (valorphin) with some opiate activity. Int. J. Pept. Protein Res. 1992, 39, 477–484.
  25. Blishchenko, E.; Sazonova, O.; Surovoy, A.; Khaidukov, S.; Sheikine, Y.; Sokolov, D.; Ivanov, V. Antiproliferative action of valorphin in cell cultures. J. Pept. Sci. Off. Publ. Eur. Pept. Soc. 2002, 8, 438–452.
  26. Blishchenko, E.Y.; Mernenko, O.A.; Mirkina, I.I.; Satpaev, D.K.; Ivanov, V.S.; Tchikin, L.D.; Ivanov, V.T. Tumor cell cytolysis mediated by valorphin, an opioid-like fragment of hemoglobin β-chain. Peptides 1997, 18, 79–85.
  27. Song, C.; Rahim, R.T.; Davey, P.C.; Bednar, F.; Bardi, G.; Zhang, L.; Zhang, N.; Oppenheim, J.J.; Rogers, T.J. PKC mediates-opioid receptor-induced cross-desensitization of chemokine receptor CCR5. J. Biol. Chem. 2011, 286, 20354–20365.
  28. Blishchenko, E.Y.; Sazonova, O.V.; Kalinina, O.A.; Moiseeva, E.V.; Vass, A.A.; Karelin, A.A.; Ivanov, V.T. Antitumor effect of valorphin in vitro and in vivo: Combined action with cytostatic drugs. Cancer Biol. Ther. 2005, 4, 125–131.
  29. Karelin, A.A.; Philippova, M.M.; Karelina, E.V.; Ivanov, V.T. Isolation of endogenous hemorphin-related hemoglobin fragments from bovine brain. Biochem. Biophys. Res. Commun. 1994, 202, 410–415.
  30. Moeller, I.; Lew, R.A.; Mendelsohn, F.A.; Smith, A.I.; Brennan, M.E.; Tetaz, T.J.; Chai, S.Y. The globin fragment LVV-hemorphin-7 is an endogenous ligand for the AT4 receptor in the brain. J. Neurochem. 1997, 68, 2530–2537.
  31. Murillo, L.; Piot, J.M.; Coitoux, C.; Fruitier-Arnaudin, I. Brain processing of hemorphin-7 peptides in various subcellular fractions from rats. Peptides 2006, 27, 3331–3340.
  32. Moisan, S.; Harvey, N.; Beaudry, G.; Forzani, P.; Burhop, K.E.; Drapeau, G.; Rioux, F. Structural requirements and mechanism of the pressor activity of Leu-Val-Val-hemorphin-7, a fragment of hemoglobin β-chain in rats. Peptides 1998, 19, 119–131.
  33. Wei, F.; Zhao, L.; Jing, Y. Hemoglobin-derived peptides and mood regulation. Peptides 2020, 127, 170268.
  34. Hung, H.Y.; Chow, L.H.; Kotlinska, J.H.; Drabik, A.; Silberring, J.; Chen, Y.H.; Huang, E.Y. LVV-hemorphin-7 (LVV-H7) plays a role in antinociception in a rat model of alcohol-induced pain disorders. Peptides 2021, 136, 170455.
  35. Ali, A.; Baby, B.; Soman, S.S.; Vijayan, R. Molecular insights into the interaction of hemorphin and its targets. Sci. Rep. 2019, 9, 1–16.
  36. Ali, A.; Alzeyoudi, S.A.R.; Almutawa, S.A.; Alnajjar, A.N.; Al Dhaheri, Y.; Vijayan, R. Camel hemorphins exhibit a more potent angiotensin-I converting enzyme inhibitory activity than other mammalian hemorphins: An in silico and in vitro study. Biomolecules 2020, 10, 486.
  37. Caballero, J. Considerations for docking of selective angiotensin-converting enzyme inhibitors. Molecules 2020, 25, 295.
  38. Amanat, A.; Soman, S.S.; Vijayan, R. Dynamics of camel and human hemoglobin revealed by molecular simulations. Sci. Rep. 2022, 12, 122.
  39. Ojima, I.; Lin, S.; Wang, T. Recent advances in the medicinal chemistry of taxoids with novel beta-amino acid side chains. Curr. Med. Chem. 1999, 6, 927–954.
  40. Mortensen, U.H.; Raaschou-Nielsen, M.; Breddam, K. Recognition of C-terminal amide groups by (serine) carboxypeptidase Y investigated by site-directed mutagenesis. J. Biol. Chem. 1994, 269, 15528–15532.
  41. Pogozheva, I.D.; Przydzial, M.J.; Mosberg, H.I. Homology modeling of opioid receptor-ligand complexes using experimental constraints. AAPS J. 2005, 7, E434–E448.
  42. Gademann, K.; Hintermann, T.; Schreiber, J.V. Beta-peptides: Twisting and turning. Curr. Med. Chem. 1999, 6, 905–925.
  43. Fülöp, F. The chemistry of 2-aminocycloalkanecarboxylic acids. Chem. Rev. 2001, 101, 2181–2204.
  44. Todorov, P.; Peneva, P.; Tchekalarova, J.; Georgieva, S.; Rangelov, M.; Todorova, N. Structure–activity relationship study on new Hemorphin-4 analogues containing steric restricted amino acids moiety for evaluation of their anticonvulsant activity. Amino Acids 2020, 52, 375–1390.
  45. Todorov, P.; Peneva, P.; Georgieva, S.; Tchekalarova, J.; Rangelov, M.; Todorova, N. Synthesis and characterization of new 5,5’-dimethyl- and 5,5’-diphenylhydantoin-conjugated hemorphin derivatives designed as potential anticonvulsant agents. New J. Chem. 2022, 46, 2198–2217.
  46. Todorov, P.; Georgieva, S.; Peneva, P.; Tchekalarova, J. Spectral and electrochemical solvatochromic investigations of newly synthesized peptide-based chemosensor bearing azobenzene side chain bio photoswitch. Dye. Pigment. 2021, 91, 109348.
  47. Todorov, P.; Georgieva, S.; Staneva, D.; Peneva, P.; Grozdanov, P.; Nikolova, I.; Grabchev, I. Synthesis of new modified with Rhodamine B peptides for antiviral protection of textile materials. Molecules 2021, 26, 6608.
  48. Todorov, P.; Peneva, P.; Pechlivanova, D.; Georgieva, S.; Dzhambazova, E. Synthesis, characterization and nociceptive screening of new VV-hemorphin-5 analogues. Bioorganic Med. Chem. Lett. 2018, 28, 3073–3079.
  49. Todorov, P.; Rangelov, M.; Peneva, P.; Todorova, N.; Tchekalarova, J. Anticonvulsant evaluation and docking analysis of VV-Hemorphin-5 analogues. Drug Dev. Res. 2019, 80, 425–437.
  50. Todorov, P.; Peneva, P.; Tchekalarova, J.; Rangelov, M.; Georgieva, S.; Todorova, N. Synthesis, characterization and anticonvulsant activity of new series of N-modified analogues of VV-Hemorphin-5 with aminophosphonate moiety. Amino Acids 2019, 51, 10–12.
  51. Assenov, B.; Pechlivanova, D.; Dzhambazova, E.; Peneva, P.; Todorov, P. Antinociceptive Effects of VV-Hemorphin-5 Peptide Analogues Containing Aminophosphonate Moiety in Mouse Formalin Model of Pain. Protein Pept. Lett. 2021, 28, 442–449.
  52. Todorov, P.; Georgieva, S.; Staneva, D.; Peneva, P.; Grozdanov, P.; Nikolova, I.; Vasileva-Tonkova, E.; Grabchev, I. Study of Novel Peptides for Antimicrobial Protection in Solution and on Cotton Fabric. Molecules 2022, 27, 4770.
  53. Todorov, P.; Peneva, P.; Tchekalarova, J.; Georgieva, S. Potential anticonvulsant activity of novel VV-hemorphin-7 analogues containing unnatural amino acids: Synthesis and characterization. Amino Acids 2020, 52, 567–585.
  54. Todorov, P.; Georgieva, S.; Peneva, P.; Tchekalarova, J. Investigation of the structure–activity relationship in a series of new LVV-and VV-hemorphin-7 analogues designed as potential anticonvulsant agents. Amino Acids 2022, 54, 261–275.
  55. Georgieva, S.; Todorov, P.; Nikolov, S.; Dzhambazova, E.; Peneva, P.; Assenov, B.; Pechlivanova, D. New N-and C-modified RGD-hemorphins as potential biomedical application on Ti-surface materials: Synthesis, characterization and antinociceptive activity. Mol. Divers. 2022, 1–18.
  56. De Rosa, T.F. Maximal Electroshock Seizure (MESs) are a model of generalized tonic-clonic seizures. From: Models of Seizures and Epilepsy, 2006. In Significant Pharmaceuticals Reported in US Patents, 3rd ed.; Elsevier: Amsterdam, The Netherlands, 2007; ISBN 978-0-08-045344-6.
  57. Potschka, H. Animal models of drug-resistant epilepsy. Epileptic Disord. 2012, 14, 226–234.
  58. Gredičak, M.; Supek, F.; Kralj, M.; Majer, Z.; Hollosi, M.; Smuc, T.; Mlinaric-Majerski, K.; Horvat, Š. Computational structure–activity study directs synthesis of novel antitumor enkephalin analogs. Amino Acids 2010, 38, 1185–1191.
  59. Löscher, W.; Klotz, U.; Zimprich, F.; Schmidt, D. The clinical impact of pharmacogenetics on the treatment of epilepsy. Epilepsia 2009, 50, 1–23.
  60. Alachkar, A.; Ojha, S.K.; Sadeq, A.; Adem, A.; Frank, A.; Stark, H.; Sadek, B. Experimental Models for the Discovery of Novel Anticonvulsant Drugs: Focus on Pentylenetetrazole-Induced Seizures and Associated Memory Deficits. Current Pharm. Design 2020, 26, 1693–1711.
  61. Prasad, S.; Rao, R.B.; Balaram, P. Contrasting solution conformations of peptides containing α, α-dialkylated residues with linear and cyclic side chains. Biopolym. Orig. Res. Biomol. 1995, 35, 11–20.
  62. Liu, J.; Obando, D.; Liao, V.; Lifa, T.; Codd, R. The many faces of the adamantyl group in drug design. Eur. J. Med. Chem. 2011, 46, 1949–1963.
  63. Wanka, L.; Iqbal, K.; Schreiner, P.R. The lipophilic bullet hits the targets: Medicinal chemistry of adamantane derivatives. Chem. Rev. 2013, 113, 3516–3604.
  64. Field, M.J.; Li, Z.; Schwarz, J.B. Ca2+ channel α2-δ ligands for the treatment of neuropathic pain. J. Med. Chem. 2007, 50, 2569–2575.
  65. Bryans, J.S.; Davies, N.; Gee, N.S.; Dissanayake, V.U.; Ratcliffe, G.S.; Horwell, D.C.; O’Neill, J.A. Identification of novel ligands for the gabapentin binding site on the α2δ subunit of a calcium channel and their evaluation as anticonvulsant agents. J. Med. Chem. 1998, 41, 1838–1845.
  66. Mart, R.J.; Allemann, R.K. Azobenzene photocontrol of peptides and proteins. Chem. Commun. 2016, 52, 12262–12277.
  67. Szymanski, W.; Beierle, J.M.; Kistemaker, H.A.; Velema, W.A.; Feringa, B.L. Reversible photocontrol of biological systems by the incorporation of molecular photoswitches. Chem. Rev. 2013, 113, 6114–6178.
  68. Piotto, S.; Trapani, A.; Bianchino, E.; Ibarguren, M.; López, D.J.; Busquets, X.; Concilio, S. The effect of hydroxylated fatty acid-containing phospholipids in the remodeling of lipid membranes. Biochim. Biophys. Acta (BBA) Biomembr. 2014, 1838, 1509–1517.
  69. Mendive-Tapia, L.; Preciado, S.; García, J.; Ramón, R.; Kielland, N.; Albericio, F.; Lavilla, R. New peptide architectures through C–H activation stapling between tryptophan–phenylalanine/tyrosine residues. Nat. Commun. 2015, 6, 1–9.
  70. Chiba, T.; Li, Y.H.; Yamane, T.; Ogikubo, O.; Fukuoka, M.; Arai, R.; Matsui, N. Inhibition of recombinant dipeptidyl peptidase III by synthetic hemorphin-like peptides. Peptides 2003, 24, 773–778.
  71. Jung, K.Y.; Moon, H.D.; Lee, G.E.; Lim, H.H.; Park, C.S.; Kim, Y.C. Structure- activity relationship studies of spinorphin as a potent and selective human P2X3 receptor antagonist. J. Med. Chem. 2007, 50, 4543–4547.
  72. Todorov, P.; Peneva, P.; Tchekalarova, J.; Rangelov, M.; Georgieva, S.; Todorova, N. Synthesis, characterization and anticonvulsant activity of new series of N-modified analogues of VV-Hemorphin-5 with aminophosphonate moiety. Amino Acids 2019, 51, 10–12.
  73. Dakubo, G.D. Brain Cancer Biomarkers in Proximal Fluids. In Cancer Biomarkers in Body Fluids; Springer: Cham, Switzerland, 2019; pp. 211–218.
  74. MacDonald, S.M.; Roscoe, S.G. Electrochemical oxidation reactions of tyrosine, tryptophan and related dipeptides. Electrochim. Acta 1997, 42, 1189–1200.
  75. Bernhardt, R. Cytochromes P450 as versatile biocatalysts. J. Biotechnol. 2006, 124, 128–145.
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