1. Introduction
Albumins are proteins with high peptide sequences homology, with bovine and human albumins sharing 76% identity
[1], abundant in the circulatory system of mammals where they contribute significantly to the osmotic blood pressure
[2]. Albumins, and primarily BSA, are typically used as protein models and their binding with molecules proposed for biotechnological applications is investigated very extensively in both academic and industrial research areas
[2,3,4,5,6,7,8,9][2][3][4][5][6][7][8][9]. Structurally, albumins present two domains with at least two high-affinity binding sites, as well as other various low-affinity ones
[10].
The major physiological function of albumins is the transport of many classes of ligands, including cations, fatty acids, steroids, and amino acids present in the bloodstream to their target organs
[1,11][1][11]. Interestingly, this binding has also driven the pharmaceutical use of albumins as drug carriers
[12,13,14][12][13][14].
Albumins are quite soluble, but frequent encounters between their molecules lead to their aggregation, as ascertained for example with BSA, ref.
[15] leading to dimers and higher aggregates
[16,17][16][17], a major factor in protein function
[18] and stability
[19,20][19][20]. More in detail, electrophoretic analysis in nondenaturing gels revealed that the monomer/dimer ratio of BSA is higher than 80%
[21], but the albumin oligomerization state can be influenced by the interactions with ligands that, as observed in the case of myristic acid, when ligated to the dimers make them less stable and more prone to dissociate into monomers
[22]. Interestingly, albumin oligomerization leads to substantial amounts of β-sheet structures which are directly correlated with aggregation
[22[22][23],
23], as well as a thermal stabilization (by more than 3 °C) of the serum albumin in the dimeric form with respect to the monomer
[24].
Oxygen-containing heterocycles are an important class of molecules, that exhibit interesting biological and therapeutic activities and share structural similarity with several natural bioactive compounds
[25,26,27][25][26][27]. Among these, benzofurans have gained a considerable interest being endowed with a wide range of biological activities such as antibiotic
[28,29[28][29][30],
30], anti-inflammatory
[31], anti-parasitic
[32], anticancer
[33,34,35][33][34][35], neuroprotective and analgesic
[36] effects. As for the molecular basis of the anticancer activity of benzofurans, the nucleic acid binding
[37], as well as the inhibition of particular serine/threonine kinases involved in tumour development, and cancer cell cycle modifications are some of the proposed mechanisms
[34,38][34][38].
Some of us have recently investigated the biological properties of compounds containing 4-nitrophenyl-functionalized benzofuran (BF) and benzodifuran (BDF) moieties, finding that both classes were endowed with antiproliferative activity on prostatic tumour cells (PC-3) in direct correlation with the lipophilicity of the heterocycles, with the compounds denominated BDF1 and especially BF1 (
Figure 1) being the most active candidates
[38]. As a prosecution of that previous work, we decided to investigate the ability of both 4-nitrophenyl-functionalized benzofuran and benzodifuran derivatives to interact with proteins, using as a model bovine serum albumin (BSA), for a better comprehension of the analogies and differences that the heteroaromatic derivatives display with respect to the binding with this fundamental family of biomacromolecules involved in numerous therapeutically relevant pathways.
Figure 1.
Chemical structures for the compounds studied as protein ligands in the current work.
2. CD Binding Studies on BSA in Complex with BF1 and BDF1
It is well known that the BSA secondary structure is mainly dominated by α-helix structures, which account for approximately 60% of its structure, while β–sheet content is less than 10%
[57][39]. Accordingly, in our experiments, the far-UV CD spectra of unliganded BSA exhibited the characteristic features of the typical helical structure of the proteins with two negative bands at 208 and 222 nm (
Figure 2, blue). After addition of BF1, the signal intensity at 208 nm was slightly greater than at 222 nm (line dark green), which suggested an increase in β-sheet content in the protein structure as a consequence of the interaction with the ligand as reported in the literature for similar spectral changes
[58][40]. On the other hand, the addition of the benzodifuran BDF1 led to the spectral curve in red (
Figure 2), which did not show any predominant band between 208 and 222 nm.
These evidences suggest that the secondary structure of BSA underwent slight but significant modifications as consequence of the binding with BF1 and BDF1, with the former being able also to increase slightly the β-sheet content of the albumin structure. To achieve a more quantitative information on this aspect, we then performed a deconvolution of the CD spectra and reported the variations of secondary structure contents of BSA in the absence and presence of an excess of benzofurans, as shown in Table 1.
Figure 2. (
a) CD spectra of BSA (0.12 μM, blue) and its complexes with the benzofuran derivatives (25 nmol) BF1 (dark green) and BDF1 (red) in 90 mM NaCl, 1.8 mM KCl, 6.6 mM Na
2HPO
4, and 1.2 mM KH
2PO
4 (pH = 7.5) at 20 °C. (
b) Zoomed-in view of the CD bands between 200–235 nm.
Table 1. Variation in BSA structure content (%) determined by benzofuran ligands. Please note that even though only minor changes can be detected after ligand binding, BF1 determines an increase in β-sheet more significant than BDF1.
|
Δ(BF1-BSA) (%) |
Δ(BDF1-BSA) (%) |
α |
+0.06 |
−0.79 |
β |
+5.70 |
+1.00 |
Random coil |
−5.76 |
−0.21 |
According to this table, BDF1 provoked only minor secondary structure changes of BSA, while a certain increase in β-sheet (+5.70%) was observed in the case of the complex of the albumin with BF1 confirming our initial analysis and the literature considerations on the increase in the 208 nm/222 nm band ratio
[58][40]. To investigate the effect of the two classes of benzofurans on protein stability, we recorded CD denaturation curves monitoring the CD values at 222 nm vs. temperature (
Figure 3a).
Figure 3. CD thermal denaturation curves [CD
222 (mdeg) vs. T (°C)] (
a) and first derivatives vs. T (
b) plots for BSA (0.12 μM, blue) and its complexes with the benzofuran derivatives (25 nmol) BF1 (green) and BDF1 (red) in 90 mM NaCl, 1.8 mM KCl, 6.6 mM Na
2HPO
4, and 1.2 mM KH
2PO
4 (pH = 7.5) at 20 °C.
By examining the first derivative maximum of the melting curves, we could demonstrate that while BDF1 led to a slight destabilization (by less than 1 °C) of BSA structure, BF1 increased melting temperature (Tm) by about 3 °C (Figure 3b, Table 2).
Table 2. Summary table of the melting temperatures (Tm) and their variations (ΔTm) with their respective error bars, with respect to the unliganded protein1 for the complexes BF1-BSA and BDF1-BSA.
Compound |
T | m | /°C |
ΔT/°C = (T | m | − T | m | BSA) |
BF1-BSA |
72.9 ± 0.1 |
+3.1 ± 0.2 |
BDF1-BSA |
69.0 ± 0.2 |
−0.8 ± 0.1 |
1 TmBSA = 69.8 ± 0.1 °C.
Taken together, the CD binding and melting studies suggested that only BF1 increases BSA β-sheet content and thermal stability, which are both features related to BSA oligomerization. Conversely, BDF1 does not significantly affect the structure elements rate in the albumin and does not provoke any thermal stabilization. This experimental evidence could be explained assuming that in binding to monomeric BSA, BDF1 prevents its aggregation, and/or that its interaction with dimer albumin does affect protein dimerization favouring dissociation into monomeric BSA, in analogy to other literature reports
[22].
3. Fluorescence Studies
Fluorescence spectroscopy was also used by us to confirm BSA complex formation with BF1 and BDF1 and to have more quantitative information on the affinities of the ligands for the protein target. The fluorescence method is a sensitive tool to study the interactions between proteins such as BSA and small molecules. The molecular recognition of BSA by small molecules mainly determines a static quenching, with the fluorescence being quenched due to the formation of complexes between the fluorophore and quenchers in the ground state
[59][41]. In general, proteins contain three fluorophores, i.e., the amino acids L-tryptophan, L-tyrosine and L-phenylalanine.
Due to the low quantum yield of L-phenylalanine and almost quenched characteristics of L-tyrosine, the intrinsic protein fluorescence occurs mainly due to the L-tryptophan. BSA possesses two L-tryptophan residues, Trp-134 and Trp-213. While this latter is situated within a hydrophobic binding pocket of the protein, Trp-134 is found on the surface in the hydrophilic region of the molecule
[60][42]. In our experiment, when exciting at 280 nm, the BSA showed a strong emission band at 347 nm. Interestingly, both compounds led to albumin fluorescence quenching (
Figure 4a,b) and their interaction was associated with a good affinity with dissociation rates (k
D) in the nanomolar range, with BF1 showing a higher affinity than BDF1 (k
D = 28.4 ± 10.1 nM vs. 142.4 ± 64.6 nM, insets of
Figure 4a,b). More in detail, the BSA emission band was monitored after adding the ligands. Successive additions of benzofurans to BSA led to significant changes in the fluorescence emission. The fluorescence intensity of BSA decreased and blue-shifted by about 10 nm with the addition of increasing amounts of both ligands. The fluorescence quenching, along with the blue shifts, are indicative of the formation of a complex between the BSA and ligands. Additionally, the formation of the complex between the albumin and both benzofurans is indicative of changes of the L-tryptophan environment. After subtracting the DMSO (dimethyl sulfoxide) emission spectrum (as background signal), the fluorescence values were plotted as functions of the concentrations, and from the data fitting it was possible to calculate the apparent k
D, as reported in the insets of
Figure 4a,b.
Figure 4. Fluorescence titrations of BSA (120 nM) with (
a) BDF1, and (
b) BF1 with ligand concentrations from 30 to 480 nM. Insets: changes in the normalized fluorescence intensity as a function of ligand concentrations (nM) for the titrations of BSA with BDF1 and BF1, after the DMSO background subtraction. k
D values with standard deviations determined by the fluorescence method are also reported here.