Calcium- and Integrin-Binding Protein 2 (CIB2)

Version	Summary	Created by	Modification	Content Size	Created at	Operation
1		Giuditta Dal Cortivo	--	3345	2022-04-21 15:37:54	\|
2	layout	Camila Xu	Meta information modification	3345	2022-04-22 03:56:27	\|

This entry is adapted from the peer-reviewed paper 10.3390/ijms23073552

Calcium- and integrin-binding protein 2 (CIB2) is a small EF-hand protein capable of binding Mg²⁺ and Ca²⁺ ions. Its biological function remains largely unclear, an increasing number of studies have shown that CIB2 is an essential component of the mechano-transduction machinery that operates in cochlear hair cells. In addition, CIB2 has been implicated in a multitude of very different processes, ranging from integrin signaling in platelets and skeletal muscle to autophagy, suggesting extensive functional plasticity.

non-syndromic deafness Usher syndrome hearing integrin signaling

1. Introduction

More than two decades ago, Seki et al. isolated from a cDNA library of human fetal brains a clone encoding a 187 amino acid protein, initially named kinase interacting protein 2 and currently referred to as calcium-and integrin-binding protein 2 (CIB2)^[1]. Examination of the transcript highlighted a broad distribution in various human tissues, including brain (both fetal and adult), heart, kidney, lung, thymus, spleen, placenta, ovary, and testis, thus suggesting that the product of the CIB2 gene is involved in basic cellular functions^[1]. Further studies also confirmed a broad expression of CIB2 in mice, specifically in the inner ear, outer and inner retina, retinal pigmented epithelium^[2], and skeletal muscle, with higher expression levels in sarcolemma, the myotendinous junction, and the neuromuscular junction in adult mice and lower expression in brain and lungs^[3]. Evidence of CIB2 expression has also been reported in adult rat brain, with specific localization in the hippocampus and in the sensory, entorhinal, and prefrontal cortex, with significant intracellular localization at the Golgi apparatus and neurites^[4]. High expression levels of the ortholog CIB2 in sheep have been found by RT-PCR in different tissues, mainly stomach, heart, and ovary^[5].

The extremely wide expression of CIB2 in various tissues of different organisms suggests its implication in a wide variety of biochemical processes. A broad and multifaceted biological function is consistent with its membership in the CIB family of Ca²⁺- and Mg²⁺-binding proteins^[6]. This family includes homologous proteins showing evolutionary relationships with the class of neuronal calcium sensors (NCS)^[7]. The biological role of CIB2 was initially associated with its interaction with specific integrins involved in intra- and extracellular signaling pathways^[3]^[8]. More recently, however, increasing lines of evidence have associated CIB2 with hearing physiology and pathology^[9], suggesting that CIB2 is an essential component for the normal development of hair cells in the inner ear and possibly a structural component of the hair cell mechanotransduction complex^[10]^[11]. In parallel, biochemical and biophysical studies^[12]^[13]^[14] have highlighted similarities but also important differences between CIB2 and other members of the CIB family, which should be considered when investigating its versatile and still largely unknown functions and involvement in processes as diverse as autophagy^[15], cancer^[16], and muscular dystrophy^[3].

2. Structural, Biochemical, and Biophysical Properties of CIB2

The discovery of the CIB gene family dates back to the 1990s, with the identification of the first member named calcium- and integrin-binding protein (CIB1)^[17] or KIP (kinase interacting protein)^[18] based on the putative function, which showed 58% sequence similarity with calcineurin B and 56% with calmodulin. Since then, several structural studies^[13]^[19]^[20] have clarified the features shared by the CIB family members, which contain three further homologs, CIB2, CIB3, and CIB4, in the human genome, and highlighted commonalities with the neuronal calcium sensor proteins (NCS) family.

Human CIB2 (NG_033006) is a 33,929 bp gene located on chromosome 15 (15q25.1) encoding four different isoforms, consisting of 4–6 exons [2]. The canonical sequence (Uniprot code: O75838-1) encodes a 187 amino acid protein of 21.6 kDa harboring two functional EF-hands, the metal-binding helix–loop–helix motif characterizing the largest family of Ca²⁺-binding proteins in eukaryotic cells^[21]. Functional EF-hands are located at the C-terminal domain of CIB2 and will be referred to as EF3 and EF4 in this research to distinguish them from the non-functional EF1 and EF2 located in the N-terminal domain (Figure 1). The three-dimensional structure of CIB2 is currently unknown, although homology models have been built based on the experimental structure of CIB1^[14] and CIB3^[20].

Figure 1. Sequence and structural properties of CIB2 and its pathogenetic variants. Top: multiple amino acid sequence alignment of human CIB1, CIB2, CIB3, and CIB4 performed by T–Coffee (https://tcoffee.crg.eu/apps/tcoffee/index.html, accessed on 22 February 2022). Consensus sequence and similarity descriptors are reported in grey text. Residues target of pathogenetic point mutations are grey-shaded in case of nonsense mutations or marked in red and blue-boxed in case of missense mutations. EF-hand motifs are displayed by colored boxes, and residues involved in Ca²⁺-coordination are indicated by letters referring to the canonical pentagonal bipyramidal geometry on the respective loops. Bottom: Representation of the three-dimensional structure of human CIB2 based on the homology model used in ^[14]. Cartoon and surface representation are superposed. The N-terminal region is colored gray, while the C-terminal region (helix 10) is colored yellow. EF1, EF2, EF3, and EF4 are colored green, slate blue, orange, and pink, respectively. Residue targets of pathogenic missense mutations are represented by magenta sticks, and Ca²⁺ ions are represented by red spheres.

2.1. CIB2 Has the Potential to Work as a Ca²⁺ and Mg²⁺ Sensor Protein

Since its discovery and based on the homology with CIB1, CIB2 was expected to act as a Ca²⁺ sensor, thereby changing its conformation upon the binding of Ca²⁺ ions and possibly other cations and acquiring a structure that allows the regulation of specific molecular targets. Human CIB2 was, therefore, heterologously expressed in E. coli and purified to study its structural and biophysical properties. Huang et al. confirmed that CIB2 acts as a typical EF-hand calcium sensor, which undergoes a significant Ca²⁺ induced conformational change, thereby exposing a hydrophobic patch and increasing the content of secondary structure—essentially α-helix—as proven by far-UV circular dichroism (CD) spectroscopy^[13]. Interestingly, the protein was also shown to respond to Mg²⁺ with similar intensity, although 8-anilinonaphthalene-1-sulfonic acid (ANS) fluorescence showed that the most prominent conformational change in terms of exposure of hydrophobic surface was observed in the presence of Ca²⁺, a result confirmed by a subsequent independent study^[14]. Nuclear magnetic resonance (NMR) spectroscopy (¹H-¹⁵N-HSQC NMR) showed that in the absence of any cation (apo- condition), the structure of CIB2 is not ordered, while far-UV CD spectroscopy demonstrated residual α-helix secondary structure. The addition of either Mg²⁺ or Ca²⁺ induced a well-folded tertiary structure in CIB2, with many peaks overlapping despite the detectable structural difference among the cation-bound specific state^[13]. An independent study was performed under similar conditions, after removing the poly-His-tag used in ^[13] for protein purification purposes, and led to very similar results, indicating that apo-CIB2 lacks tertiary structure and forms a molten globule state, as also confirmed by near-UV CD spectroscopy^[14].

2.2. An Alleged Ca²⁺ Sensor? CIB2 Constitutively Binds Mg²⁺ but Has Low Affinity for Ca²⁺

In vitro studies showed that all CIB proteins respond to Mg²⁺ and Ca²⁺ stimuli in a relatively similar manner in terms of general structural features^[13]; however, a recent investigation by Vallone et al. highlighted important peculiarities of CIB2 in cation-sensing^[14]. NMR titration experiments reporting on the Ca²⁺ binding state of specific residues suggested that when starting from the apo-protein, EF3 is the first EF-hand in CIB2 to be occupied by Ca²⁺, followed by EF4. The variation of ¹H-¹⁵N HSQC peak intensity for the EF4 residue Gly 162 upon Ca²⁺ titration experiments displays a sigmoidal shape, indicative of positive cooperativity^[14]. However, in the presence of physiological levels of free Mg²⁺ (approximately 1 mM), EF3 seems never to be occupied by Ca²⁺ but rather constitutively Mg²⁺-bound. A Mg²⁺/Ca²⁺ exchange would thus possibly occur only in EF4^[14] (Figure 2).

Figure 2. Schematic representation of CIB2 cation sensitivity and structural transitions. (a) In the absence of cations, WT CIB2 is in a molten globule state (left). The addition of a physiological concentration of both Mg²⁺ and Ca²⁺ (middle top panel) triggers the binding of Mg²⁺ in EF3 and EF4. In the presence of physiological Ca²⁺ and absence of Mg²⁺ (middle bottom panel), Ca²⁺ binding is less favorable. When extra (non-physiological) Ca²⁺ concentrations are added, Ca²⁺ replaces Mg²⁺ in EF4 (upper right panel). (b) E64D CIB2 is in a molten globule state under physiological conditions (left). A well-defined three-dimensional structure is acquired upon the addition of extra (non-physiological) Mg²⁺ (upper right panel) or Ca²⁺ (bottom right panel), with a more pronounced effect for Ca²⁺. The Wi-Fi logo represents the strength of allosteric interactions between E64 and N121 residues.

While a similar conclusion was also previously drawn for CIB1^[22], there is an important difference between the two proteins. The apparent affinity for Ca²⁺ of CIB2 is as low as 500 μM^[14] while significantly higher affinity was measured for Ca²⁺ binding to CIB1, (K_d = 0.5 μM for EF4; K_d = 1.9 μM for EF3^[22]^[23]), which makes its Ca²⁺ sensing capabilities similar to those of calmodulin^[24]. Moreover, Mg²⁺ binding is limited to the EF3 loop in the case of CIB1 (K_d = 120 μM^[22]^[23]), but it appears to involve both EF3 and EF4 in the case of CIB2 (apparent affinity: 290 μM^[14]). The physiological consequence is clear when these values are considered in the context of intracellular levels of the two cations. Intracellular Ca²⁺ oscillates in the 0.1–10 μM range^[25], and in specific cell compartments such as the outer segments of photoreceptors, where CIB2 has also been detected [2], it reaches even lower values^[26]^[27]. On the other hand, free Mg²⁺ is generally constant in most cells and ranges in the 0.5–1 mM interval^[28]^[29]. Overall, this suggests that CIB1 can indeed work as a Ca²⁺ sensor under physiological Ca²⁺ levels, while CIB2 would keep two Mg²⁺ ions constitutively bound to both functional EF-hands, being substantially insensitive to intracellular Ca²⁺ oscillations (Figure 2). It is to be noticed that based on a TNS fluorescence (2-p-toluidinylnaphthalene-6-sulphonate) assay, Blazejczyk et al.^[4] reported a much higher affinity (K_d = 0.14 μM) for Ca²⁺ for GST-fused CIB2. This value is in contrast to data obtained with untagged CIB2 from direct spectroscopic analyses performed by NMR and CD titrations and indirect competition assays with 5,5′-Br₂-BAPTA^[14] and could be affected by artifacts induced by the interaction with the bulky (26 kDa) fused GST moiety.

The relatively low affinity for Ca²⁺ of CIB2, distinguishing it from CIB1, is not surprising if its primary structure is considered (Figure 1). The structure of CIB1^[19] reveals an optimal pentagonal bipyramid geometry offered by oxygen-coordinating Ca²⁺ in EF4 due to the presence of an Asn residue (N169) in the -X position of the coordinating loop and to a Glu residue in the -Z position (E172), which constitutes a bidentate ligand for Ca²⁺ that is broadly conserved among EF-hand motifs^[30]^[31]. At odds, -X and -Z positions in CIB2 are occupied, respectively, by the side-chain-lacking G165 and by D168, which cannot act as a bidentate ligand due to the shorter side chain. This likely distorts the geometry of the whole loop and results in a lower affinity for Ca²⁺^[14]. Important differences are also found in EF3, which explains the lower affinity for Ca²⁺ of this loop for CIB2 compared to CIB1. A negatively charged residue (D118) occupies the Y coordinating position in CIB1, while a neutral one (N118) is substituted in CIB2, thus preventing a favorable coulombic interaction; moreover, the ninth position (-X) in the EF-hand loop is occupied by an Asn (N124) in CIB1 and by the least frequently observed Cys residue (C124), known for destabilizing some EF-hands^[32]. The sequence of CIB2 is, therefore, not evolutionary optimized for Ca²⁺ binding.

The presence of physiological targets is known to significantly tune the metal affinity of Ca²⁺ sensors, often increasing it, such as in the case of myristoylated recoverin, a prototypical NCS protein in which the co-presence of the GRK1 target and the membrane is required to bring the Ca²⁺ sensitivity into the physiological range, thus enhancing over 100-fold the apparent Ca²⁺ affinity with respect to the isolated protein^[33]. In the case of CIB2, the presence of a membrane-proximal peptide from the cytoplasmic domain of the α7B integrin was shown to double the apparent affinity for Ca²⁺ (K_d^app = 200 μM vs. 500 μM in the absence of the target)^[14]. While significant per se, this change does not support the physiological role of CIB2 as a Ca²⁺ sensor, unless the microenvironment of specific cell compartments and the co-presence of other factors such as myristoylation, membrane, or other supramolecular complexes will prove otherwise by enhancing the apparent affinity of CIB2 for Ca²⁺.

2.3. An Inter-Domain Allosteric Switch Regulates the Conformational Transitions of CIB2

Although with a lower affinity than CIB1, CIB2 binds Mg²⁺ and Ca²⁺ (the latter under non-physiological conditions), and this significantly stabilizes the structure of the protein. Thermal denaturation studies performed by monitoring the protein secondary structure content by far-UV CD spectroscopy indeed proved that apo-CIB2 is rather unstable, with a melting temperature (T_m) of 35 °C, while the addition of Mg²⁺ or Ca²⁺ significantly increases the stability by enhancing the T_m of 11 and 8 °C, respectively^[14]. In the co-presence of both cations, the T_m resembles that of Mg²⁺, confirming the minor stabilizing role of Ca²⁺ compared to Mg²⁺. The stabilizing effects of cations on the protein tertiary structure are even more apparent when analyzed by NMR, which also highlighted an important allosteric mechanism connecting EF3 with the non-functional EF1 motif. An inter-domain allosteric communication was detected between the EF3 binding loop and the residue E64, which is predicted to form an electrostatic interaction with R33, thereby contributing to the stability of the EF1 subdomain. This was clearly demonstrated by ¹H-¹⁵N HSQC NMR spectra, where the chemical shift of N121 in EF3 and E64 in EF1 were found to show the same pattern upon Ca²⁺-titration experiments. The switch that allows CIB2 to acquire a functional conformation at physiological levels of Mg²⁺ seems, therefore, to be finely regulated by an allosteric, long-range communication connecting EF1 with EF3 (Figure 2a). Interestingly, E64 is mutated into an Asp (E64D) in a group of patients affected by Usher syndrome type 1 J^[2]. Vallone et al. demonstrated that the apparently conservative E64D substitution breaks up such inter-domain communication, resulting in a protein that is unable to bind Mg²⁺, which is necessary to adopt the required physiological conformation, thus providing a first mechanistic explanation for the molecular basis of disease^[14].

2.4. CIB2 Is Monomeric, but It Could Dimerize in the Presence of a Target

Analytical size exclusion chromatography (SEC) is a valuable technique to study the hydrodynamic properties of proteins, and it can be used to assess the molecular weight (MW) of the eluting protein when a calibration curve is obtained in the same conditions for a number of globular proteins is available^[34]. The apparent MW of CIB2 obtained by SEC in the presence of Mg²⁺ or co-presence of Mg²⁺ and Ca²⁺ was determined to be around 39 kDa, therefore significantly higher the theoretical MW of a monomer (22 kDa); this was initially interpreted as evidence of the dimeric nature of CIB2^[14]. A similar conclusion was supported by dynamic light scattering (DLS) measurements. A subsequent study employing a variety of mass spectrometry (MS)-based techniques, including native ESI-MS, MALDI-TOF-MS, and cross-linking/MS integrated with novel SEC and DLS experiments based on a more accurate selection of the heterogeneous components of the elution bands, demonstrated that CIB2 was monomeric under all tested conditions^[12]. A comparison with results obtained with recoverin and calmodulin suggested that the apparent MW, extrapolated by analytical SEC for a Ca²⁺ sensor protein and based on the hydrodynamic radius, can significantly differ from the real value when the protein has a high hydrophobic solvent-accessible surface, such as in the case of recoverin and CIB2^[12]. Analytical SEC could then be driven to erroneous conclusions as to the oligomeric state of the protein^[14]. This can explain the apparent contradiction with previous studies that detected CIB2 dimers based on FRET and co-immunoprecipitation. In these studies, CIB2 was fused to GFP^[2]^[35] or tdTomato fluorescent protein^[2]; its uncommon hydrodynamic properties, together with a possible interference of the bulky fusion constructs, may have led to the erroneous detection of a dimer^[12]. The most recent and thorough dedicated investigation performed with untagged purified CIB2 seems to exclude the existence of CIB2 dimers under conditions mimicking the physiological ones^[12]. In this respect, the oligomeric state of CIB2 resembles that of CIB1. Ca²⁺-bound CIB1 was indeed found to be monomeric in the crystallographic structure reported by Gentry et al.^[19], and this finding has been supported by NMR diffusion, SEC, and sedimentation equilibrium experiments^[36]^[37]. The head-to-tail dimer reported by another crystallographic study could result from the specific conditions for crystal formation, which included a GSH moiety at the N-domain^[38].

Surface plasmon resonance (SPR) spectroscopy also excluded the dimerization of CIB2 over a broad range of conditions, including selective incubation with Mg²⁺ and Ca²⁺^[12], but suggested an interesting mechanism of binding to integrin. The formation of a protein–peptide complex between CIB2 and a peptide from the α7B integrin was shown to possibly drive the binding of a second CIB2 molecule; the process seems to be kinetically favored in the sole presence of Mg²⁺^[12]. Although this hypothesis awaits confirmation, the mechanism of target-induced CIB2 dimerization would explain the 2:1 protein:peptide stoichiometry detected for the same interaction in a previous fluorescence study ^[14], and it is tempting to speculate that it might play a role in the integrin signaling mediated by CIB proteins.

2.5. CIB2 Myristoylation

Myristoylation is a post-translational modification operated by the N-myristoyl transferase that, in vivo, covalently binds a 14-carbon saturated fatty acid (myristoyl moiety) to the N-terminal glycine of proteins harboring the consensus sequence MGXXXS/T^[39]. CIB1, CIB2, and CIB3 have the optimal consensus sequence (Figure 1) and are likely to be myristoylated in vivo, while CIB4 is not. The binding of Ca²⁺ ions to some NCS proteins triggers the so-called “myristoyl switch” mechanism, which extrudes the myristoyl moiety from a hydrophobic cleft in the protein milieu to a fully solvent-exposed state, thus allowing membrane-binding and permitting specific cell localization and target interaction^[40].

It is not clear whether CIB1 undergoes a Ca²⁺-induced myristoyl-switch, as contrasting conclusions have been reported by different groups. Jarman et al.^[41] concluded that the myristoyl switch mechanism occurs in CIB1, and it is necessary to translocate the sphingosine kinase 1 (SK1) target to the membrane; in contrast, according to Blazejczyk et al., the myristoyl moiety of CIB1 is likely solvent-exposed rather than buried within the protein, regardless of its Ca²⁺ binding state^[42]. Whether or not the Ca²⁺-induced switching mechanism occurs, the myristoylation of CIB1 is still important for protein stability and membrane targeting^[43]^[44], as well as shuttling its binding partners to the membrane^[41]^[45]. Myristoylation-deficient CIB1 variants retain a high affinity for target proteins and peptides both in vitro and in vivo^[42]^[44]^[46]^[47], thus suggesting that the myristoyl group is not specifically involved in target recognition.

Much less information is available about the myristoylation of CIB2. Blazejczyk et al.^[4] expressed GFP-tagged CIB2 and a myristoylation-blocking variant (^G2ACIB2-GFP) in COS-7 cells in the presence of radioactive ³H-myristic acid and compared the effect of CIB2 myristoylation with that of VILIP1-GFP^[48], known to undergo the Ca²⁺-induced myristoyl switch, thereby resulting in specialized membrane compartment localization. In contrast to what was observed for VILIP1-GFP, no Ca²⁺-dependent translocation was detected for CIB2-GFP, which was interpreted as a lack of Ca²⁺-induced myristoyl switch^[4]. Moreover, localization of CIB2 was essentially limited to the crude membrane fraction, regardless of the tag (CIB2-FLAG gave the same results) and, surprisingly, of myristoylation as the same behavior was detected for ^G2ACIB2-GFP^[4]. This would exclude a direct association of CIB2 to the membrane by myristoyl anchoring and rather suggests that the binding is mediated directly by lipids or by an interaction with other proteins. Within COS-7 cells, CIB2 co-localizes with the Golgi apparatus and not with the nucleus, and the absence of myristoylation does not affect this pattern^[4].

An independent study by Zhu et al.^[49] confirmed that CIB2 does not undergo a Ca²⁺-induced myristoyl switch and blocks the agonist-induced membrane translocation of SK1, at odds with the activity of CIB1. Experiments were performed with HA-tagged CIB2 in HEK293 cells labeled with ³H-myristic acid and showed that the interaction of CIB2 with SK1 was independent of the presence of Ca²⁺ or Mg²⁺. Further experiments are needed to elucidate the biological role of CIB2 myristoylation, and biophysical studies may clarify the structural and mechanistic aspects that remain somewhat unclear.

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Giuditta Dal Cortivo

Daniele Dell'Orco

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Table of Contents

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1. Introduction

2. Structural, Biochemical, and Biophysical Properties of CIB2

2.1. CIB2 Has the Potential to Work as a Ca²⁺ and Mg²⁺ Sensor Protein

2.2. An Alleged Ca²⁺ Sensor? CIB2 Constitutively Binds Mg²⁺ but Has Low Affinity for Ca²⁺

2.3. An Inter-Domain Allosteric Switch Regulates the Conformational Transitions of CIB2

2.4. CIB2 Is Monomeric, but It Could Dimerize in the Presence of a Target

2.5. CIB2 Myristoylation

References

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1. Introduction

2. Structural, Biochemical, and Biophysical Properties of CIB2

2.1. CIB2 Has the Potential to Work as a Ca2+ and Mg2+ Sensor Protein

2.2. An Alleged Ca2+ Sensor? CIB2 Constitutively Binds Mg2+ but Has Low Affinity for Ca2+

2.3. An Inter-Domain Allosteric Switch Regulates the Conformational Transitions of CIB2

2.4. CIB2 Is Monomeric, but It Could Dimerize in the Presence of a Target

2.5. CIB2 Myristoylation

References

2.1. CIB2 Has the Potential to Work as a Ca²⁺ and Mg²⁺ Sensor Protein

2.2. An Alleged Ca²⁺ Sensor? CIB2 Constitutively Binds Mg²⁺ but Has Low Affinity for Ca²⁺