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A Novel Trans Conformation of Ligand-Free Calmodulin

  • Veerendra Kumar,

    Affiliation Department of Biological Sciences, National University of Singapore, Republic of Singapore, Republic of Singapore

  • Vishnu Priyanka Reddy Chichili,

    Affiliation Department of Biological Sciences, National University of Singapore, Republic of Singapore, Republic of Singapore

  • Xuhua Tang,

    Affiliation Department of Biological Sciences, National University of Singapore, Republic of Singapore, Republic of Singapore

  • J. Sivaraman

    dbsjayar@nus.edu.sg

    Affiliation Department of Biological Sciences, National University of Singapore, Republic of Singapore, Republic of Singapore

A Novel Trans Conformation of Ligand-Free Calmodulin

  • Veerendra Kumar, 
  • Vishnu Priyanka Reddy Chichili, 
  • Xuhua Tang, 
  • J. Sivaraman
PLOS
x

Abstract

Calmodulin (CaM) is a highly conserved eukaryotic protein that binds specifically to more than 100 target proteins in response to calcium (Ca2+) signal. CaM adopts a considerable degree of structural plasticity to accomplish this physiological role; however, the nature and extent of this plasticity remain to be fully understood. Here, we report the crystal structure of a novel trans conformation of ligand-free CaM where the relative disposition of two lobes of CaM is different, a conformation to-date not reported. While no major structural changes were observed in the independent N- and C-lobes as compared with previously reported structures of Ca2+/CaM, the central helix was tilted by ∼90° at Arg75. This is the first crystal structure of CaM to show a drastic conformational change in the central helix, and reveals one of several possible conformations of CaM to engage with its binding partner.

Introduction

Calmodulin (CaM), a 16.7 kDa protein found in all eukaryotic cells, has been extensively studied as a primary calcium (Ca2+)-binding protein [1]. CaM mediates various processes, including inflammation, metabolism, apoptosis, smooth muscle contraction, intracellular movement, short-term and long-term memory, nerve growth, cell motility, growth, proliferation and the immune response [2]. The function of CaM is affected by post-translational modifications, such as phosphorylation, acetylation, methylation and proteolytic cleavage [3]. CaM consists of two homologous (46% sequence identity) globular lobes; each has a pair of Ca2+ binding sites (EF-hand motifs), connected by a flexible linker [4]. Each EF-hand motif comprises two α helices connected by a 12-residue loop (helix-turn-helix) and provides a suitable electronegative environment for Ca2+ ion coordination. The helices of two EF-hands motifs create a Phe and Met-rich hydrophobic pocket that is exposed to solvent and involved in target binding [5]. In apo CaM (Ca2+ free), the α-helices in the EF-hand motifs are positioned almost parallel to each other (closed conformation), whereas in the presence of Ca2+, the α-helices of the EF-hand motifs change their position relative to each other, forming an almost perpendicular conformation (open conformation) [6], [7]. Ca2+ therefore induces a large conformational change, exposing the hydrophobic surface and facilitating binding between Ca2+/CaM and a number of basic amphiphilic helices on target proteins [8]. The central helix of CaM is highly flexible and is the key to its ability to bind a wide range of targets [9].

Conformational flexibility plays a key role in CaM function. CaM is able to adopt a wide variety of conformations for its interaction with different targets [10], [11], [12], [13], [14]. The N- and C-terminal lobes move in to wrap around the hydrophobic residues of a target molecule [10], [11]. Besides this classical mode of binding, CaM bound to oedema factor adopts an extended conformation [12]. In other cases, part of the central α-helix transforms into loops to facilitate peptide interactions [13], [14], or binding to the target peptide occurs only via the C-terminal lobe [15], [16]. Moreover, NMR and other spectroscopic studies have shown that the central α-helix is flexible in solution, and the backbone atoms between residues Lys77-Asp80 undergo conformational changes [17]. Although CaM is best characterized to specifically bind with Ca2+, a number of studies have indicated that it can also bind with other metal ions [18], [19], [20]. Besides, CaM is able to selectively bind Ca2+ despite the fact that, in the resting cell, there are high levels of other cations, especially magnesium (Mg2+), which is present in roughly a 102–104-fold higher concentration than intracellular Ca2+ [21]. Zinc (Zn2+) antagonizes the calcium action by inhibiting the same cellular reactions triggered by Ca2+. This inhibition occurs through binding of Zn2+ to the CaM-protein complex [22].

The calpacitin protein family members, neuromodulin (Nm) and neurogranin (Ng), are intrinsically unstructured proteins, and are shown to interact with apo CaM (Ca2+ free). In the present study, the IQ peptides derived from Nm and Ng were present in the crystallization drops; however, no electron density was observed to confirm the existence of complex in the crystal. This crystal structure of CaM, in which no substrate peptide was bound (hereafter referred as ligand-free CaM), adopts a unique trans conformation that has so far not been observed.

Materials and Methods

CaM Expression and Purification

The CaM (accession no NP_033920) gene was cloned into the pETDuet-1 expression vector (Novagen, Madison, WI) at the cloning site 1, following standard procedures. The recombinant plasmid (pETDuet-CaM) was transformed into chemically competent E. coli BL21 (DE3) cells for the large-scale protein production. The cells were grown in 1 L of LB media, and the cell pellet was obtained by centrifugation at 9800 g. Cell pellets were re-suspended in 100 ml of lysis buffer composed of 50 mM Tris-HCl (pH-8.0), 500 mM NaCl, 10% v/v glycerol, 20 mM imidazole, 20 mM BME and 0.1 mM PMSF, and lysed by sonication. The cell lysate was centrifuged at 39,000 g for 30 min at 4°C. The supernatant was mixed with 5 ml of Ni–NTA resin (Qiagen, Valencia, CA) for 2 h at 4°C. Ni–NTA resin was washed thrice using 10 ml of lysis buffer each time. Subsequently, the bound proteins were eluted from Ni-NTA beads using lysis buffer supplemented with 300 mM imidazole (pH 8.0). Next, the eluted CaM was passed through the gel filtration column, HiLoad™ 16/60 Super- dex™ 75 prep grade (Amersham Biosciences, Uppsala, Sweden) in a buffer containing 20 mM HEPES (pH 8.0), 100 mM NaCl and 10 mM CaCl2. The protein was concentrated up to 12 mg/ml and taken for crystallization experiments. The selenomethionine-labeled proteins were produced using LeMaster media [23] following a similar procedure as described above. All protein purification steps were carried out at 4°C, unless otherwise stated.

Crystallization and Structure Determination

The commercially synthesized IQ motifs of Nm (34AATKIQASFRGHITRKKLKGEKKG57) and Ng (27NAAAAKIQASFRGHMARKKIKSGE50) were present in the crystallization mixture in the molar ratio of 1∶3 (CaM: peptide). The initial objective of this work was to crystallize CaM as a complex with these peptides. However, we obtained only the crystals of CaM. The crystallization experiments were conducted at room temperature using hanging drop vapor diffusion method. The initial crystallization conditions obtained from PACT Suite (Qiagen) were further optimized. The diffraction quality crystals of ligand-free CaM were obtained using a reservoir solution consisting of 100 mM Tris-HCl (pH 8.0), 8–10% v/v PEG 6 K, 5–10 mM ZnCl2 and 10% v/v glycerol. Crystals were directly picked from drop and flash-cooled in N2 cold stream at 100 K.

Brief attempts with molecular replacement method did not yield any structure solution; this led us to collect the Single-wavelength Anomalous Dispersion (SAD) dataset in the synchrotron beam line X8C (NSLS, Brookhaven National Laboratory, Upton, New York) using a Quantum 4-CCD detector (Area Detector Systems Corp Poway, CA, USA) and processed using HKL2000 [24]. Heavy atom (Se) location, phasing and density modification were performed using the program ShelxC/D/E [25], and model building was carried out with the program Buccaneer [26] in CCP4. When necessary, the model was manually built in COOT [27] and refinement was performed in Refmac5 [28]. At the final stage of refinement, well-ordered water molecules were included. The model had good stereochemistry, as analyzed by PROCHECK [29] (Table 1). All structure-related figures reported in this manuscript were prepared using PyMol [30].

Protein Data Bank Accession Code

Coordinates and structure factors of the ligand-free Ca2+/Zn2+/CaM has been deposited with RCSB Protein Data Bank with codes 4HEX.

Results and Discussion

Overall Structure

The crystal structure of ligand-free CaM was determined by Single-wavelength Anomalous Dispersion (SAD) method and refined to an R-factor of 0.20 (Rfree = 0.23) up to 2.02 Å resolution. The electron density for the N-terminal His-tag and the first 5 residues were not well-defined and were therefore not included in the model. The model had good geometry, with no residues in the disallowed region of the Ramachandran plot (Table 1). There are two identical molecules (RMSD 0.7 Å) in the asymmetric unit (Supplementary Figure S1). However, the PISA server [31] analysis and gel filtration chromatography suggest that ligand-free CaM is a monomer. The Ca2+ ions were well-defined in the electron density map, located at each EF-hand motif. Besides a Zn2+ ion was observed near His108 for the first time in CaM. The ligand-free CaM molecule was in an open conformation, wherein helices of EF motifs were perpendicular to each other (Figure 1).

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Figure 1. A novel trans conformation of calmodulin (CaM).

A: Ribbon representation of novel conformation of ligand-free CaM. The helices, loops, Ca2+ and Zn2+ are shown in blue, pale green, green and grey, respectively. The CaM molecule adopts an extended dumbbell-shaped conformation and the two domains are well separated. The bending at Arg75 is shown in stick representation. The α-helices are numbered from I-VIII. B: 2Fo-Fc electron density map for the region 65–80 aa of CaM. This map is contoured at a level of 1σ.

https://doi.org/10.1371/journal.pone.0054834.g001

Calmodulin Adopts a Novel Conformation

A search for structural homologs in the PDB database using the DALI program [32] did not identify any similar structures. In the present structure, the ligand-free CaM adopts a unique conformation, with the relative disposition of the two lobes being completely different to any of the previously reported CaM structures (Figure 2). However, a one-to-one comparison of individual domains showed no significant structural differences (rmsd less than 0.8 Å for all Cα atoms). The structurally similar two lobes were in trans conformation about the axis of the central helix (Figures 2 and 3).

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Figure 2. Comparison among various calmodulin (CaM) structures.

A: The Cα superposition of the present study novel trans conformation of CaM with several extended (trans) CaM conformations: 1PRW (magenta), 2F2P (white), 2W73 (red), and 3CLN (dark salmon). B: The Cα superposition of present study novel trans conformation of CaM with several wrapped (cis) CaM conformations: 2BE6 (yellow), 2F3Y (light blue), 2O60 (pale green), 2VAY (teal), 2X0G (orange), 3BXK (deep purple), 3DVE (gray), 1CDM (olive). CaM conformations can be classified as “wrapped” and “extended”. In “wrapped” conformation, the two lobes are close to each others in cis orientation. In “extended” conformation, the two lobes are widely separated in trans orientations. In the present study, CaM adopted a novel trans conformation. The positions of metal ions in the current structure (blue) are labeled as Ca2+ (Green) and Zn2+ (grey). These structure alignments were carried out in PyMol [30].

https://doi.org/10.1371/journal.pone.0054834.g002

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Figure 3. Comparison of cis and trans conformations of Calmodulin.

A: Side-by-side comparison of the novel trans (current structure, blue) and cis (pdb code 1PRW, magenta) conformations of CaM, which show the unwinding region of central helix in both structures in cyan and yellow, respectively. B: Side-by-side comparison of the novel trans (current structure, blue) and extended trans (pdb code 3CLN, dark salmon) conformations of CaM. In the extended trans conformation of CaM, no unwinding of the central helix was observed. The positions of the metal ions in the current novel trans (blue) are labeled as Ca2+ (Green) and Zn2+ (grey). In wrapped cis (1PRW, magenta) and extended trans (3CLN, dark salmon), all sites (EF1-EF4) were occupied by Ca2+ (Green).

https://doi.org/10.1371/journal.pone.0054834.g003

A close examination of the current ligand-free CaM structure with previously reported CaM complexes showed that residues Ala74-Asp79 of the central helix (aa 65–92) are unwound, and bent by ∼90° near Arg75; this reoriented the C-lobe in a perpendicular direction to the central helix (Figure 1 and 2). While a transformation of α-helix to loops has been previously reported [13], [14], the kink observed at Arg75 is unique. This unique structure of CaM represents one of its many possible conformations. The side chain of Arg75 is exposed on the surface of the molecule, which makes four hydrogen bonding contacts only with symmetry-related molecules (Arg38 and Arg127). The B-factors are the indicators of ordered nature of the atoms. The average B-factors for Arg75 of chain A and B are 47.5 and 50.9 Å2, respectively. These average values are in good agreement with the B factors of the neighbouring residues, and suggest that Arg75 is well ordered (Figure 1). A detailed study of Lys76 mutation on CaM conformation was carried out by Medvedeva et al. [33]. A double mutation, containing a KGK insertion between residues 81 and 82, and a point mutation of K76P, makes the central helix highly flexible in Ca2+/CaM, as determined by the trypsinolysis [33]. Two mutants (K76P and K76E) were regarded as having a distorted central helix, and showed high resistance to trypsinolysis in the absence of Ca2+ [33]. Mutants K76A and K76V, on the other hand, decreased the rate of trypsinolysis of the central helix with a simultaneous increase in the rate of trypsinolysis in the C-terminal domain of CaM [33]. These studies revealed that various mutations in the central helix alter the conformation of CaM and confirm the highly flexible nature of the central helix, as observed through NMR studies [17].

Previously, a closed, compact crystal structure of CaM (PDB 1PRW) was reported at 1.7 Å resolution [34]. In this structure, CaM existed in a compact ellipsoidal conformation and revealed a sharp bend in the central helix. The two lobes were in cis orientation, in contrast to the trans orientation observed in the current study. The N-lobe and C-lobe were close to each other and made several inter-domain contacts (Figure 3). The residues Asp79-Ser82 were unwound and made a type 1 reverse turn [34]. The complex structure of CaM and IQ peptide from Lc-, P/Q-, and R-type voltage-dependent Ca2+ channels is similar, wherein the central helix of CaM unwinds and peptides are wrapped by two lobes of CaM ( [35], [36]; 3BXK and 3BXL). Similarly, the structure of apo CaM bound to the first two IQ motifs of the murine myosin V heavy chain adopts a unique conformation, in which central helix unwinds and the N and C lobes wrap around the peptides [37].

All the above CaM complex structures adopt a cis conformation. However, in the current study, the conformation of CaM was in an extended form, and the two globular lobes were widely separated. As noted above, residues Ala74-Asp79 were unwound by one turn and formed a sharp bend at Arg75. However, incubating Nm/Ng or their IQ peptides with Ca2+/CaM did not show any spectral changes to indicate any conformational change in CaM [38]. Nonetheless, the observed conformation of CaM in this study represents a novel trans structure of CaM. The implication of this conformation is yet to be studied. The bending of the central helix is a key feature of the conformational dynamics of CaM in recognizing the target [9].

It has to be noted that the Ca2+/CaM (buffer supplemented with 10 mM CaCl2) crystals were grown in conditions containing 5–10 mM ZnCl2. A previous flow dialysis study showed that CaM has two higher (80–300 µM) affinity Zn2+ ion sites and four or five lower affinity Zn2+-binding sites [22], [39]. Nevertheless, the previously reported Zn2+-bound, N-lobe CaM structure resembles the apo CaM structures (i.e. the closed form of CaM) [39]; by comparison, CaM adopts an open form in the current structure. Further, no similar bend at Arg75 was observed in the previous structure despite Zn2+ binding to both EF-hand motifs in the N-lobe [39]. Based on the heavy atom peak heights in the anomalous map and the refinement statistics comparison (R-values and B-factors) we assigned the observed electron density as Ca2+ ions in the EF-hand motifs and a Zn2+ ion near His108 (Figure 4). However the possibility of having less occupancy Zn2+ that might mimic a fully occupied Ca2+ cannot be ruled out. We have observed that lowering the ZnCl2 concentration in crystallization conditions reduces the nucleation and results in good quality crystals. The observed Zn2+ ion at chain A is coordinating with His108, Lys95 (chain A), Asp81 and Glu81 (chain B) and vice versa for chain B. A similar coordination for Zn2+ ion has been reported in ALE-1, a glycylglycine endopeptidase from Staphylococcus capitis EPK1 [40].

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Figure 4. Coordination of Zn2+ ion: A Zn2+ ion (grey) bound to His108 and Lys95 of chain A (magenta), and Asp81 and Glu85 from chain B (blue).

A similar Zn2+ ion is also present in chain A.

https://doi.org/10.1371/journal.pone.0054834.g004

In CaM, Ca2+ binding occurs sequentially, first in the C-lobe followed by N-lobe binding. C-lobe has much higher affinity for Ca2+ than does the N-lobe. Ca2+ binding to CaM rearrange the EF motifs in each lobe, central helix becomes α helical but no such bend has been observed [6], [41], [42]. Previously, the Ca2+ in Ca2+/CaM crystals was replaced by Pb2+ and Ba2+ by soaking. The crystal structures of Pb2+/CaM and Ba2+/CaM did not show large conformational changes as compared with Ca2+/CaM [43], [44]. Thus, the present conformational change observed in the central helix of the CaM is independent of the bound metal ions. The large conformational changes in proteins are often associated with ligand/partner binding. One proposed function for Nm and Ng is to sequester CaM at the membrane in the vicinity of ‘CaM-activated enzymes’ under low Ca2+ conditions at the pre- and post-synaptic terminals, respectively. Elevations of intracellular free Ca2+ would promote dissociation of CaM from Nm and Ng [45]. We speculate that upon Ca2+ binding to CaM-Nm/Ng, CaM might undergo some conformational change, similar to the one reported here, to release Nm/Ng. This has to be approached cautiously and warrants experimental verification.

In summary, CaM is known to interact with over 100 different proteins to modulate their activity, adopting various conformations to engage with its binding partners. In the present study no electron density for the IQ peptide was observed to confirm the existence of its complex in the crystal; thus, only the ligand-free CaM was crystallized. The observed ∼90° bend at the central α-helix near Arg75 may represent a key conformational dynamics of CaM essential for engaging its target. This study reveals a novel trans conformation of CaM as one of many possible conformations that has so far not been observed.

Supporting Information

Figure S1.

This diagram shows the packing of the symmetry-related molecules in the crystal. The two molecules of the asymmetric unit were shown in blue and magenta respectively. The nearest symmetry related molecules shown in different colors.

https://doi.org/10.1371/journal.pone.0054834.s001

(TIF)

Acknowledgments

X-ray diffraction data for this study were measured at beamline X8C at BNL, New York, USA. Veerendra Kumar is a graduate scholar in receipt of a research scholarship from the National University of Singapore (NUS).

Author Contributions

Conceived and designed the experiments: JS VK. Performed the experiments: VK VPRC. Analyzed the data: VK VPRC XT JS. Wrote the paper: VK JS.

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