research papers
The structure of the cysteine protease and lectin-like domains of Cwp84, a surface layer-associated protein from Clostridium difficile
aDepartment of Biology and Biochemistry, University of Bath, Claverton Down, Bath BA2 7AY, England, and bPublic Health England, Porton Down, Salisbury SP4 0JG, England
*Correspondence e-mail: bsskra@bath.ac.uk
Clostridium difficile is a major problem as an aetiological agent for antibiotic-associated diarrhoea. The mechanism by which the bacterium colonizes the gut during infection is poorly understood, but undoubtedly involves a myriad of components present on the bacterial surface. The mechanism of C. difficile surface-layer (S-layer) biogenesis is also largely unknown but involves the post-translational cleavage of a single polypeptide (surface-layer protein A; SlpA) into low- and high-molecular-weight subunits by Cwp84, a surface-located cysteine protease. Here, the first of the surface protein Cwp84 is described at 1.4 Å resolution and the key structural components are identified. The truncated Cwp84 active-site mutant (amino-acid residues 33–497; C116A) exhibits three regions: a cleavable propeptide and a cysteine protease domain which exhibits a cathepsin L-like fold followed by a newly identified putative carbohydrate-binding domain with a bound calcium ion, which is referred to here as a lectin-like domain. This study thus provides the first structural insights into Cwp84 and a strong base to elucidate its role in the C. difficile S-layer maturation mechanism.
Keywords: Clostridium difficile; surface layer-associated protein; Cwp84.
PDB reference: Cwp84, 4ci7
1. Introduction
Disruption of the normally protective gut flora results in the extensive colonization and growth of Clostridium difficile (Guarner & Malagelada, 2003), a predominantly nosocomially acquired Gram-positive, spore-forming bacterium. C. difficile infection (CDI) can lead to severe diarrhoea, pseudomembranous colitis, toxic megacolon and ultimately death (Kachrimanidou & Malisiovas, 2011; Rupnik et al., 2009). In recent years, CDI has become a global burden both medically and economically (Bouza, 2012; Dubberke & Olsen, 2012).
C. difficile expresses a self-assembling paracrystalline protein array on its outermost surface, known as an S-layer. The S-layer is largely derived from the post-translational cleavage of a single polypeptide (surface-layer protein A; SlpA) into low- and high-molecular-weight subunits (LMW SLP and HMW SLP, respectively) by Cwp84, a surface-located cysteine protease (Calabi et al., 2001; Cerquetti et al., 2000; Karjalainen et al., 2001; Kirby et al., 2009).
The HMW SLP contains three putative cell-wall binding/anchoring domains (CWBDs; Pfam 04122) which are thought to mediate noncovalent binding to the bacterial cell surface via a currently unknown mechanism. A total of 28 S-layer paralogues, including Cwp84, containing three Pfam 04122 repeats at either the N-terminal or C-terminus with a `functional' domain at the other end, have been identified in the C. difficile genome (Calabi et al., 2001; Fagan et al., 2011; Monot et al., 2011; Sebaihia et al., 2006).
A number of these putative surface proteins have been found to play key roles in cell physiology and adhesion (Kirby et al., 2009; Reynolds et al., 2011; Waligora et al., 2001), and have been demonstrated to illicit an in vivo during infection (Wright et al., 2008). Using the ClosTron gene-knockout system, we have demonstrated that a number of C. difficile surface-associated genes containing Pfam 04122 repeats may play a role in adhesion in vitro and may also affect the release of the potent C. difficile toxins, particularly Cwp84 (Kirby et al., unpublished work).
Cwp84 (cell-wall protein ∼84 kDa) is an 803-residue surface-associated protein containing a cysteine protease domain at the N-terminus, a linker region of roughly 170 residues of unknown function and three Pfam 04122 repeats (Fig. 1a; Janoir et al., 2004, 2007). Cwp84 has been shown to be responsible for the maturation of the SlpA precursor protein (Dang et al., 2010; de la Riva et al., 2011; Kirby et al., 2009) and has also been implicated in the degradation of extracellular matrix proteins such as fibronectin, laminin and vitronectin (Janoir et al., 2007).
Despite the key role played by Cwp84 in S-layer biogenesis, it has been reported that neither chemical inhibition of Cwp84 (Dang et al., 2010) nor inactivation of the cwp84 gene (de la Riva et al., 2011; Kirby et al., 2009) is bactericidal, although severe growth defects were seen in both cases. These results indicate that correct maturation of SlpA by Cwp84 is vital to maintain healthy bacterial cells; perturbing this process may therefore affect the ability of the bacterium to thrive in vivo and thus compete with other bacterial species in certain environments, such as in the complex microbiome of the intestine. Nevertheless, in a hamster model of acute infection we previously showed that a cwp84 knockout strain of C. difficile was not attenuated for virulence and suggested that endogenous within the intestinal tract may artificially mature/cleave SlpA (Kirby et al., 2009). However, our unpublished observations suggest that C. difficile toxin release is altered in the cwp84 mutant, which may negate severe growth defects (Kirby et al., unpublished work). Even so, it has been speculated that the interruption of S-layer biogenesis may make the bacterium more susceptible to antibiotics (Dang et al., 2010). This makes Cwp84 a potential target for novel prophylactic or therapeutic drugs against CDI, the development of which would be guided by structural analyses of the protein.
Cwp84 is a member of the C1A cysteine protease family (Rawlings et al., 2010), also known as papain with a putative catalytic dyad comprising of residues Cys116 and His262, aided by Asn287 (Savariau-Lacomme et al., 2003). Recently, Dang and coworkers showed that Cwp84 containing the substitution Cys116Ala did not cleave SlpA in an Escherichia coli-based co-expression assay, confirming that Cys116 is a catalytically important residue (Dang et al., 2010). Papain peptidases are typically composed of an N-terminal signal peptide, a propeptide and the After the removal of the signal peptide by a signal peptidase, the proenzyme often (but not always; Dahl et al., 2001; Nägler et al., 1999) undergoes self-cleavage, removing the proregion and generating the mature, active enzyme (Beton et al., 2012; ChapetónMontes et al., 2011). It has been proposed that the propeptide ensures the correct folding of the protein (ChapetónMontes et al., 2011). A recent study by de la Riva and coworkers showed that Cwp84 is produced as an inactive proenzyme and is processed into the active enzyme of 77 kDa by removal of the signal peptide and proregion up to Ser92 and that this activation step is unlikely to be autocatalytic (de la Riva et al., 2011).
Despite adherence and subsequent colonization by C. difficile representing key milestones in infection, there are considerable gaps, particularly with regard to structural data, in the understanding of how the surface proteins of C. difficile interact with each other and their environment. To date, there has only been one previous report of structural information for a C. difficile surface protein, which presented the of an N-terminal fragment of the low-molecular-weight subunit of the S-layer at 2.4 Å resolution (PDB entry 3cvz) and structures based on solution-scattering (SAXS) experiments of both full-length LMW SLP and the complex formed by LMW SLP and HMW SLP (Fagan et al., 2009).
To further the understanding of C. difficile S-layer biogenesis, we report a high-resolution (1.4 Å) of the N-terminal cysteine protease domain of Cwp84. Interestingly, the hitherto uncharacterized 170-residue `linker' region between the cysteine protease domain and putative location of the first Pfam 04122 repeat exhibits a lectin-like domain structure with a bound calcium ion.
2. Materials and methods
2.1. Protein expression and purification
A synthetically synthesized gene encoding C. difficile Cwp84 residues 33–497 (from strain QCD32g-58; ribotype 027) with a C116A mutation (an inactive mutant; Life Technologies GeneArt Ltd) was cloned by PCR into the GST expression vector pGEX-6P-1. The mutation was introduced to potentially circumvent problems with poor expression and degradation or problems with purification (based on initial trials with multiple constructs designed without the mutation). Of the two constructs produced with the mutation, neither had the problems discussed above and one was purified to near-homogeneity in one step (see below). The structure presented in this manuscript made use of this particular construct.
The gene was amplified from the stock pMA vector by PCR with Expand High Fidelity polymerase (Roche) utilizing primers incorporating cleavage sites for BamHI at the 5′ end and NotI at the 3′ end preceded by a TAA stop codon (forward primer GAGAGTCCTCGGATCCCACAAAACCCTGGATGGCGTGGAA, reverse primer CTCTCTCGCGGCCGCTCTTAGCTGGTTTTGGTGATCGCTT). The PCR products were digested with BamHI and NotI (NEB) and cloned into pGEX-6P-1 using T4 DNA ligase (New England Biolabs) to generate pGEX-6P-1-Cwp8433–497C116A.
The plasmid was transformed into E. coli BL21*(DE3) cells. Cultures were grown from glycerol stocks in 5 ml LB supplemented with 100 µg ml−1 ampicillin for 17 h and centrifuged (5000g, 10 min). The cell pellets were washed with water, centrifuged a second time, resuspended in water and used to inoculate 500 ml selenomethionine medium (Molecular Dimensions) supplemented with 100 µg ml−1 ampicillin. These cultures were grown with shaking (200 rev min−1, 37°C) to an OD600 of 0.7. The temperature was reduced to 16°C and methionine production was inhibited by the addition of 100 µg ml−1 lysine, phenylalanine and threonine and 50 µg ml−1 leucine, isoleucine and valine. 60 µg ml−1 selenomethionine was also added and the cultures were incubated for 15 min before expression was induced with 1 mM IPTG. The cultures were incubated for a further 18 h and harvested by centrifugation (8000g, 10 min).
The cell pellets were resuspended in PBS (140 mM NaCl, 2.7 mM KCl, 5 mM DTT, 10 mM Na2HPO4, 1.8 mM KH2PO4 pH 7.3), lysed in a French press and clarified by centrifugation (75 000g, 25 min). The supernatant was loaded onto a GSTrap column (GE Healthcare) and washed with PBS, and tagged protein was eluted with 10 mM glutathione, 50 mM Tris–HCl pH 8.0. PreScission protease (80 µl) was added and the eluted protein was dialyzed overnight into cleavage buffer (50 mM Tris–HCl, 150 mM NaCl, 1 mM EDTA, 5 mM DTT pH 7.5). The dialyzed sample was then reloaded onto the GSTrap column to separate the unbound protein from the tag.
Unbound protein was concentrated to a volume of roughly 1 ml and further purified by M Tris–HCl pH 8.0 (using a Superdex 200 16/600 column); fractions containing Cwp8433–497C116A were pooled and concentrated to 11.9 mg ml−1.
(SEC) into 50 m2.2. Trypsin cleavage of Cwp84
GST-Cwp8433–497 was incubated with trypsin at a molar ratio of approximately 10:1 for 45 min. Following purification by SEC in 25 mM MOPS pH 7.0, the resulting single species (Cwp8492–497) was analysed by electrospray ionization Cwp8492–497 was also transferred onto PVDF and sent for N-terminal sequencing (AltaBioscience).
2.3. X-ray crystallographic studies
Crystallization-condition screening was performed with a range of pre-prepared 96-well screens (Molecular Dimensions) using an Art Robbins Phoenix nanodispensing robot. Optimal conditions were reproduced with 0.3 µl drops with a 1:1 ratio of protein to reservoir solution (0.2 M ammonium sulfate, 30% PEG 4K; Molecular Dimensions Structure Screen 1 & 2, solution D7). Crystals took between 3 d and a week to grow.
X-ray diffraction data were collected at station I03 at Diamond Light Source (DLS; Didcot, Oxfordshire, England). The diffraction data were recorded with 1.0° oscillation on a Pilatus 6M detector from four crystals to obtain maximum redundancy. Selenium-fluorescence peak and inflection data were collected from all four crystals (to a maximum resolution of 1.73–1.87 Å), while high and low remote data were collected from two crystals (to a maximum resolution of 1.94–2.16 Å). 1120 peak images were collected at 12 660 eV, 1120 inflection images at 12 656 eV, 540 low-remote images at 12 550 eV and 540 high-remote images at 12770 eV. The data were automatically indexed and integrated with XDS (Kabsch, 2010) and xia2 (Winter et al., 2013), respectively. The data were scaled (and resolutions cut to those reported in Table 1 to reduce errors) with SCALA (Diederichs & Karplus, 1997), combined with CAD (CCP4; Winn et al., 2011) and put into the Crank MAD pipeline (CCP4; Ness et al., 2004) with a resolution cutoff of 2.5 Å using SCALEIT (Howell & Smith, 1992), AFRO (CCP4), CRUNCH2 (de Graaff et al., 2001), BP3 (Pannu et al., 2003; Pannu & Read, 2004), SOLOMON (Abrahams & Leslie, 1996) and 500 cycles of Buccaneer/REFMAC (Cowtan, 2006; Murshudov et al., 2011). CRUNCH2 found 55 potential selenium sites out of a predicted 48 within the the validity of which was determined with the later programs, allowing Buccaneer and REFMAC to produce an output model with a figure of merit of 85.6% and Rcryst and Rfree values of 24.8 and 27.7%, respectively. The model was further refined with Coot/REFMAC (Emsley & Cowtan, 2004) using a 1.4 Å resolution native data set collected on a Pilatus 6M on I02 at DLS that had been autoprocessed with XDS and xia2 and scaled with AIMLESS (Evans, 2006). Secondary structure was determined using DSSP (Kabsch & Sander, 1983) and the model was verified with MolProbity (Chen et al., 2010).
|
The atomic coordinates and structure-factor amplitudes have been deposited with the RCSB Protein Data Bank (https://www.pdb.org) under PDB accession code 4ci7.
3. Results
3.1. Overview
We have determined the ). This combination of a cysteine protease domain and a `lectin-like' domain appears to be present in a number of species within the Clostridiales order and is also seen in a small number of archaea (Fig. 2), as revealed by a BLASTP search using Cwp8433–497 from strain 630, suggesting conservation of this particular domain arrangement. DALI searches using the whole structure did not reveal any proteins within the PDB with structural similarity over both domains.
of a truncated Cwp84 active-site mutant, residues 33–497, which comprises the propeptide, the cysteine protease domain and the newly identified `lectin-like' domain (Fig. 1The high-resolution structure was solved in the monoclinic P21 to 1.4 Å resolution with two molecules in the crystallographic It was refined to final Rcryst and Rfree values of 13.8 and 16.9%, respectively, and also contained two calcium ions, two sulfate ions, eight PEG molecules, six glycerol molecules and 927 water molecules, with an estimated solvent content of 43.8%. Calcium ion identities were determined by their ability to fill electron density and were confirmed through coordinate bond lengths (Harding, 2004; Zheng et al., 2008). Overall, 96.1% of the residues are in the preferred regions of the Ramachandran plot, with 3.9% in the allowed regions and no outliers. The crystallographic statistics are summarized in Table 1. Poor electron density was observed between residues Gly58 and Tyr63, although we were able to interpret this part of the structure with a fair degree of certainty; little to no density was observed between Lys81 and Tyr89, so this region was not built in the structure (Fig. 3a).
3.2. Propeptide
The propeptide largely consists of loop regions with a central helix (α1) and short β-strand (β1). The poorly defined region was determined to contain a short helix in chain B but not in chain A: our secondary-structure numbering assumes that this helix is not present.
The N-terminal portion of the Cwp84 propeptide (His33–Gly65) wraps around the lectin-like domain (Figs. 1b and 1c) and does not exhibit similarities to propeptides from other papain which commonly form a small globular domain covering the top of the active site and are stabilized by a β-sheet formed by interaction with the prosegment binding loop (PBL; Figs. 4a and 4b). This novel conformation leaves the S′ end of the active-site groove (the portion of the active-site groove that interacts with the peptide substrate after the scissile bond, based on the active-site nomenclature of Sajid & McKerrow, 2002; Schechter & Berger, 1967) significantly more accessible than in other cysteine Nevertheless, the catalytic residues are partially occluded by Asn114 and Asn261 (Fig. 3e).
The C-terminal portion of the propeptide (Val66–Arg79) forms an extended loop that sits in the active-site cleft. The poorly defined helix (found only in chain B) that precedes this loop is considerably removed from the active site, around 7–8 Å away from its location in both cathepsin L and cathepsin B (Fig. 4c). Residues Asn64–Ile67 form a hydrogen-bond network with the cysteine protease domain. These interactions are mainly with Met160–Ser164, but hydrogen bonds are also formed to Asn114 and Leu260. After this, the propeptide enters the active-site groove, with Pro70–Glu72 forming hydrogen bonds to the N-terminal part of the propeptide. Thr76–Arg79 form a large number of hydrogen bonds to the lectin-like domain and the cysteine protease domain. Close interactions between the propeptide and the cysteine protease domain are seen in many other proteins (Coulombe et al., 1996; Sivaraman et al., 1999), but as the lectin-like domain is a newly observed feature of a cysteine protease, so too are its interactions with the propeptide.
There are usually two main points on a cysteine protease to which its propeptide is anchored: the surface-exposed PBL (prosegment-binding loop), which the propeptide of Cwp84 does not approach, and the S2 subsite of the active-site cleft, which is occupied by a residue that mimics the substrate (Coulombe et al., 1996; Sivaraman et al., 1999). Interestingly, in Cwp84 this latter position is occupied by Val66 from the propeptide, while the P2 residue of SlpA is usually lysine. Although Val66 is able to interact with the S2 subsite through van der Waals interactions, the shorter, hydrophobic side chain does not enter the negatively charged pocket (Fig. 3d). Given the apparent lack of PBL stabilization and the shorter Val66, the propeptide is likely to be stabilized through other multi-domain interactions.
Treatment of the purified recombinant GST-Cwp8433–497 protein (78.5 kDa) with trypsin was found to result in the loss of approximately 33.5 kDa, giving a single band of 45 kDa. The mass of this protein, as confirmed by mass-spectrometric analysis, was 45 058 Da, and therefore the loss of 33.5 kDa from the protein is consistent with removal of the proregion and GST. The N-terminal sequencing determined that the remaining 45 kDa protein had an N-terminus of SSVAY, confirming that the proregion up to Ser92 had been removed. These data suggest that the proregion is folded in Cwp8433–497 in such a way that it is accessible for cleavage by trypsin and that artificial maturation has replicated the removal of the proregion up to Ser92 as observed in C. difficile (ChapetónMontes et al., 2011; de la Riva et al., 2011).
3.3. Cysteine protease domain
The overall fold of the cysteine protease domain of Cwp84 is similar to those of other papain DALI structural similarity search (Holm & Rosenström, 2010) indicates that it shares the highest level of similarity with Toxoplasma gondii cathepsin L (Z = 23.9, sequence identity 20%; PDB entry 3f75; Larson et al., 2009), rhodesain from Trypanosoma brucei (Z = 23.6, sequence identity 21%; PDB entry 2p7u; Kerr et al., 2009) and cruzipain from T. cruzi (Z = 23.5, sequence identity 19%; PDB entry 4klb; Wiggers et al., 2013).
particularly cathepsin L-like AThe cysteine protease domain exhibits a typical, approximately U-shaped fold with two subdomains flanking the central active-site cleft, one formed by a twisted antiparallel β-sheet containing four β-strands (β4, β6, β7 and β8), one helix (α5) and several loop regions, and the other formed by a central 15-residue-long α-helix (α2) surrounded by two short α-helices (α3 and α4), an antiparallel β-sheet containing two strands (β3 and β9) and several loop regions (Fig. 2).
The active site of the cysteine protease domain of Cwp84 is similar to those of other cysteine et al., 2003), is not located within the active site.
with regard to the positions of the active-site residues Cys116 (mutated to alanine in the present study), His262 and Gln110. Asn287, which has previously been suggested to be an active-site residue (Savariau-Lacomme3.4. Lectin-like domain
We have discovered that the approximately 170-residue `linker' region between the cysteine protease domain and the first cell-wall-binding domain in full-length Cwp84 forms a single domain (residues 335–497) consisting of 13 β-strands (β10–β22), eight of which form a twisted antiparallel β-sandwich with a hydrophobic core. Proteins with similar folds to this domain were determined using a DALI search. The majority of the most similar results were carbohydrate-binding proteins, including Clostridium perfringens α-N-acetylglucosaminidase (Z = 8.1, sequence identity 14%; PDB entry 2vcc; Ficko-Blean et al., 2008), a sialidase from Micromonospora viridifaciens (Z = 8.0, sequence identity 11%; PDB entry 2bzd; Newstead et al., 2005) and a noncatalytic carbohydrate-binding module from Clostridium thermocellum (Z = 7.7, sequence identity 8%; PDB entry 2yb7; Montanier et al., 2011); we therefore designate this domain the `lectin-like' domain. There were, however, a significant number of noncarbohydrate-binding results, including E3 ubiquitin ligases such as Mus musculus MYCBP2 (Z = 9.5, sequence identity = 13%; PDB entry 3hwj; Sampathkumar et al., 2010), human DNA-repair protein XRCC1 (Z = 8.2, sequence identity 10%; PDB entry 3k77; Cuneo & London, 2010) and Chlamydomonas reinhardtii intraflagellar transport protein 25 (Z = 8.1, sequence identity 9%; PDB entry 2yc4; Bhogaraju et al., 2011). The lectin-like domain contains a calcium ion coordinated by Leu339, Glu448, Lys460, Asn487 and two water molecules. Most of the conserved residues within the lectin-like domain are found within β-strands, are hydrophobic or bind calcium (Fig. 2). This indicates that the structure and potentially the function of the lectin-like domain is conserved amongst these proteins, of which we believe this to be the first report.
The lectin-like domain contains a hydrophobic core that opens at the surface of the protein, producing a hydrophobic pocket formed by residues Ile347, Ile468, Ile477 and Phe483. Interestingly, both Leu36 and Val39 from the propeptide insert into this pocket, with Lys34 hydrogen bonding to Thr479, suggesting that these interactions may provide stabilizing roles through hydrophobic interactions.
The cysteine protease domain and the lectin-like domain also have interaction points between the two domains at three locations: Gln338, Leu457–Glu458 (Fig. 5) and Tyr408–Asn413. The glutamine residue at position 338, which is highly conserved in the BLASTP results (Fig. 2), forms an isolated hydrogen bond; Leu457–Glu458 form main-chain hydrogen bonds, while Tyr408–Asn413 make both main-chain and side-chain interactions.
Two of the three regions where the lectin-like and cysteine protease domains interact (Gln338 and Leu457–Glu458) are both sequentially and spatially close to the calcium ion-binding site (formed by Leu339, Glu448, Lys460 and Asn487).
4. Discussion
In this study, we have elucidated the structure of residues 33–497 of Cwp84, the surface-associated cysteine protease of C. difficile which plays a key role in the maturation of the S-layer protein SlpA. The high-resolution structural data presented here will improve the understanding of the role of Cwp84 in S-layer biogenesis. In addition, the discovery of a newly identified calcium-binding lectin-like (putative carbohydrate-binding) domain raises exciting possibilities with regard to the potential role(s) that this region may have in S-layer biogenesis in C. difficile and also in other species, such as those presented in Fig. 2. We also compared the structure of the cysteine protease domain (C1A family) of Cwp84 with those reported for the cysteine protease domains (C80 family) from the large clostridial toxins of C. difficile (TcdA and TcdB; Pruitt et al., 2009; Shen et al., 2011) and found no detectable structural similarity between the two classes of cysteine protease structures.
We observed that the cysteine protease domain retains a strong structural similarity to other papain-family enzymes, namely the cathepsins, particularly cathepsin L. However, significant differences exist between Cwp84 and structurally similar proteases.
Cathepsin B-like 2′ position (Sajid & McKerrow, 2002). In the same position, cathepsin L-like possess a much shorter loop that does not block the active site, allowing the cleavage of a broader range of substrates (Coulombe et al., 1996). The equivalent loop in Cwp84 (found between α4 and β3) is closer to that of cathepsin L-like Although slightly longer than the usually well conserved fold, it is much shorter than the occluding loop found in cathepsin B-like and does not contain the HH motif (Fig. 4c). This loop is poorly conserved among closely related proteins (Fig. 2) and thus may be involved in substrate selectivity.
possess a long loop, known as the occluding loop, which partially blocks the S end of the active site. This allows greater endopeptidase substrate specificity and also confers carboxypeptidase activity on the protein, with a conserved HH motif in the occluding loop binding the substrate at the SThe loop formed between helix 3 and helix 4, which forms one side of the active-site cleft and has a position that is well conserved in other cysteine β-bridge with the lectin-like domain, forming one of the three contact points between the two domains (Fig. 5). The active-site cleft then continues in the S direction with one side formed by the cysteine protease domain and the other by the lectin-like domain, which, as it has not been observed in other cysteine protease structures, gives the S end of the active site a significantly different shape (Fig. 3).
is roughly 3–4 Å further away from the active site than usual. This presents a deeper active-site cleft, which may be important for substrate binding and specificity. This loop also contains two residues that form aMoreover, in papain 2 position of the active site has been shown to play a significant role in determination of substrate specificity: this position is occupied by Ser205 in papain, Ala214 in cathepsin L and Glu245 in cathepsin B (Sajid & McKerrow, 2002). In Cwp84, S2 selectivity is likely to be controlled by Asp320, which, along with Ser235, Thr317 and Asp318, forms a negatively charged pocket which is likely to stabilize the binding of the P2 lysine residue usually found in SlpA (Fig. 3d). Indeed, mutation of the P2 lysine to alanine has been shown to abolish the cleavage of an SlpA fragment by Cwp84 in co-expression studies, suggesting its significance in SlpA cleavage (Dang et al., 2010).
a residue above the SWe believe the lectin-like domain to be a newly observed feature of cysteine β-sandwiches that are closely associated with a protease domain (Adams et al., 2013). The two could possess similar functions, namely conferring resistance to degradation, positioning the prodomain for cleavage and assuring the correct conformation of the protease domain. Even though the cores of the lectin-like domains appear to have a similar structure, there are significant changes (resulting in a large root-mean-square deviation) in the positioning of the β-strands, including the loop regions. Further experimental studies will be required to confirm the role(s) of the lectin-like domain in Cwp84.
particularly those from Clostridiales. It bears some resemblance to the jelly-roll domain of the clostridial serine protease CspB, in that both areInterestingly, lectin-like interactions have been suggested to be involved in S-layer array formation, particularly with regard to the linkage between the S-layer subunits and secondary cell-wall polymers (SCWPs; Ferner-Ortner et al., 2007; Sára et al., 1998; Sára & Sleytr, 2000).
The carbohydrate-binding region seen in many of the DALI results does not appear to be present in Cwp84, indicating that if the lectin-like domain does bind it does so using a different interface. IFT25 (intraflagellar transport protein 25) has a fold almost identical to that of sialidases, but the carbohydrate-binding region is replaced by a region that interacts with a helix from IFT27 to form the IFT25/27 complex (Bhogaraju et al., 2011). In Cwp84, the equivalent region interacts with the propeptide. If the Cwp84 lectin-like domain does bind (or a different cofactor) in this region, it is possible that the propeptide prevents binding. It is also not unreasonable to assume that despite its similarity to carbohydrate-binding proteins, the lectin-like domain of Cwp84 may assume a completely different function.
We believe the close interactions between the cysteine protease domain, the lectin-like domain and the propeptide are likely to be essential to the initial folding of the protein and will mediate substrate binding and specificity.
5. Conclusions
We have determined the structure of the Cwp84 cysteine protease domain with its bound propeptide and a newly discovered lectin-like domain. The propeptide sits in the active-site groove and wraps itself around the lectin-like domain, closely interacting with both domains, a feature that is likely to be important in the initial folding of the protein. The cysteine protease domain, although similar to many previously determined cathepsin L-like structures, bears significant differences; namely, the active-site groove is deepened by the lectin-like domain, the PBL is not present and the would-be occluding loop is slightly longer. The lectin-like domain bears a similar β-sandwich fold to that seen in many carbohydrate-binding proteins, but it is currently unclear what function it possesses. If it does bind a carbohydrate, it is possible that the lectin-like domain may be involved in substrate recognition or attachment to the cell wall, resulting in correct orientation of the cysteine protease domain for cleavage of SlpA.
Further structural and functional studies are necessary to elucidate the exact mechanism of Cwp84-mediated SlpA cleavage and how this contributes to overall S-layer biosynthesis. Given the likely key role of the C. difficile surface in growth and colonization, the potential development of anti-colonization inhibitors or vaccines is significantly aided by structural data such as that presented here.
Acknowledgements
We thank the scientists at PX stations I02 and I03 of Diamond Light Source, Didcot, England for their support during X-ray diffraction data collection. This work was supported by postgraduate studentships from Public Health England (PHE, Porton Down, England) and the University of Bath to WJB, CJC and AHD, a Medical Research Council (UK) project grant (MK/K027123/1) to KRA and CCS and a Wellcome Trust (UK) equipment grant (088464) to KRA. Author contribution are as follows. WJB performed protein expression, purification and structural biology experiments, analysed the structures and wrote the manuscript. JMK performed protein expression and purification, analysed the data and edited the manuscript. NT helped with X-ray data collection and analysis. CJC performed the cloning and preliminary protein expression experiments. AHD performed preliminary analysis of X-ray diffraction data. AKR supervised some of the work and edited the manuscript. CCS conceived and supervised the study, analysed the data and edited the manuscript. KRA conceived the study, performed some of the structural work, supervised the study, analysed the data and wrote and edited the manuscript. All authors reviewed the manuscript. The authors declare no competing financial interests.
References
Abrahams, J. P. & Leslie, A. G. W. (1996). Acta Cryst. D52, 30–42. CrossRef CAS Web of Science IUCr Journals Google Scholar
Adams, C. M., Eckenroth, B. E., Putnam, E. E., Doublié, S. & Shen, A. (2013). PLoS Pathog. 9, e1003165. Web of Science CrossRef PubMed Google Scholar
Beton, D., Guzzo, C. R., Ribeiro, A. F., Farah, C. S. & Terra, W. R. (2012). Insect Biochem. Mol. Biol. 42, 655–664. Web of Science CrossRef CAS PubMed Google Scholar
Bhogaraju, S., Taschner, M., Morawetz, M., Basquin, C. & Lorentzen, E. (2011). EMBO J. 30, 1907–1918. Web of Science CrossRef CAS PubMed Google Scholar
Bond, C. S. & Schüttelkopf, A. W. (2009). Acta Cryst. D65, 510–512. Web of Science CrossRef CAS IUCr Journals Google Scholar
Bouza, E. (2012). Clin. Microbiol. Infect. 18, Suppl. 6, 5–12. Google Scholar
Calabi, E., Ward, S., Wren, B., Paxton, T., Panico, M., Morris, H., Dell, A., Dougan, G. & Fairweather, N. (2001). Mol. Microbiol. 40, 1187–1199. Web of Science CrossRef PubMed CAS Google Scholar
Cerquetti, M., Molinari, A., Sebastianelli, A., Diociaiuti, M., Petruzzelli, R., Capo, C. & Mastrantonio, P. (2000). Microb. Pathog. 28, 363–372. Web of Science CrossRef PubMed CAS Google Scholar
ChapetónMontes, D., Candela, T., Collignon, A. & Janoir, C. (2011). J. Bacteriol. 193, 5314–5321. Web of Science PubMed Google Scholar
Chen, V. B., Arendall, W. B., Headd, J. J., Keedy, D. A., Immormino, R. M., Kapral, G. J., Murray, L. W., Richardson, J. S. & Richardson, D. C. (2010). Acta Cryst. D66, 12–21. Web of Science CrossRef CAS IUCr Journals Google Scholar
Coulombe, R., Grochulski, P., Sivaraman, J., Ménard, R., Mort, J. S. & Cygler, M. (1996). EMBO J. 15, 5492–5503. CAS PubMed Web of Science Google Scholar
Cowtan, K. (2006). Acta Cryst. D62, 1002–1011. Web of Science CrossRef CAS IUCr Journals Google Scholar
Cuneo, M. J. & London, R. E. (2010). Proc. Natl Acad. Sci. USA, 107, 6805–6810. Web of Science CrossRef CAS PubMed Google Scholar
Dahl, S. W., Halkier, T., Lauritzen, C., Dolenc, I., Pedersen, J., Turk, V. & Turk, B. (2001). Biochemistry, 40, 1671–1678. Web of Science CrossRef PubMed CAS Google Scholar
Dang, T. H., de la Riva, L., Fagan, R. P., Storck, E. M., Heal, W. P., Janoir, C., Fairweather, N. F. & Tate, E. W. (2010). ACS Chem. Biol. 5, 279–285. Web of Science CrossRef CAS PubMed Google Scholar
Diederichs, K. & Karplus, P. A. (1997). Nature Struct. Biol. 4, 269–275. CrossRef CAS PubMed Web of Science Google Scholar
Dubberke, E. R. & Olsen, M. A. (2012). Clin. Infect. Dis. 55, S88–S92. Web of Science CrossRef PubMed Google Scholar
Emsley, P. & Cowtan, K. (2004). Acta Cryst. D60, 2126–2132. Web of Science CrossRef CAS IUCr Journals Google Scholar
Evans, P. (2006). Acta Cryst. D62, 72–82. Web of Science CrossRef CAS IUCr Journals Google Scholar
Fagan, R. P., Albesa-Jové, D., Qazi, O., Svergun, D. I., Brown, K. A. & Fairweather, N. F. (2009). Mol. Microbiol. 71, 1308–1322. Web of Science CrossRef PubMed CAS Google Scholar
Fagan, R. P., Janoir, C., Collignon, A., Mastrantonio, P., Poxton, I. R. & Fairweather, N. F. (2011). J. Med. Microbiol. 60, 1225–1228. Web of Science CrossRef CAS PubMed Google Scholar
Ferner-Ortner, J., Mader, C., Ilk, N., Sleytr, U. B. & Egelseer, E. M. (2007). J. Bacteriol. 189, 7154–7158. Web of Science CrossRef PubMed CAS Google Scholar
Ficko-Blean, E., Stubbs, K. A., Nemirovsky, O., Vocadlo, D. J. & Boraston, A. B. (2008). Proc. Natl Acad. Sci. USA, 105, 6560–6565. Web of Science PubMed CAS Google Scholar
Graaff, R. A. G. de, Hilge, M., van der Plas, J. L. & Abrahams, J. P. (2001). Acta Cryst. D57, 1857–1862. Web of Science CrossRef IUCr Journals Google Scholar
Guarner, F. & Malagelada, J. R. (2003). Lancet, 361, 512–519. Web of Science CrossRef PubMed Google Scholar
Harding, M. M. (2004). Acta Cryst. D60, 849–859. Web of Science CrossRef CAS IUCr Journals Google Scholar
Holm, L. & Rosenström, P. (2010). Nucleic Acids Res. 38, W545–W549. Web of Science CrossRef CAS PubMed Google Scholar
Howell, P. L. & Smith, G. D. (1992). J. Appl. Cryst. 25, 81–86. CrossRef Web of Science IUCr Journals Google Scholar
Janoir, C., Grénery, J., Savariau-Lacomme, M. P. & Collignon, A. (2004). Pathol. Biol. 52, 444–449. Web of Science CrossRef PubMed CAS Google Scholar
Janoir, C., Péchiné, S., Grosdidier, C. & Collignon, A. (2007). J. Bacteriol. 189, 7174–7180. Web of Science CrossRef PubMed CAS Google Scholar
Kabsch, W. (2010). Acta Cryst. D66, 125–132. Web of Science CrossRef CAS IUCr Journals Google Scholar
Kabsch, W. & Sander, C. (1983). Biopolymers, 22, 2577–2637. CrossRef CAS PubMed Web of Science Google Scholar
Kachrimanidou, M. & Malisiovas, N. (2011). Crit. Rev. Microbiol. 37, 178–187. Web of Science CrossRef CAS PubMed Google Scholar
Karjalainen, T., Waligora-Dupriet, A. J., Cerquetti, M., Spigaglia, P., Maggioni, A., Mauri, P. & Mastrantonio, P. (2001). Infect. Immun. 69, 3442–3446. Web of Science CrossRef PubMed CAS Google Scholar
Kerr, I. D., Lee, J. H., Farady, C. J., Marion, R., Rickert, M., Sajid, M., Pandey, K. C., Caffrey, C. R., Legac, J., Hansell, E., McKerrow, J. H., Craik, C. S., Rosenthal, P. J. & Brinen, L. S. (2009). J. Biol. Chem. 284, 25697–25703. Web of Science CrossRef PubMed CAS Google Scholar
Kirby, J. M., Ahern, H., Roberts, A. K., Kumar, V., Freeman, Z., Acharya, K. R. & Shone, C. C. (2009). J. Biol. Chem. 284, 34666–34673. Web of Science CrossRef PubMed CAS Google Scholar
Larkin, M. A., Blackshields, G., Brown, N. P., Chenna, R., McGettigan, P. A., McWilliam, H., Valentin, F., Wallace, I. M., Wilm, A., Lopez, R., Thompson, J. D., Gibson, T. J. & Higgins, D. G. (2007). Bioinformatics, 23, 2947–2948. Web of Science CrossRef PubMed CAS Google Scholar
Larson, E. T., Parussini, F., Huynh, M.-H., Giebel, J. D., Kelley, A. M., Zhang, L., Bogyo, M., Merritt, E. A. & Carruthers, V. B. (2009). J. Biol. Chem. 284, 26839–26850. Web of Science CrossRef PubMed CAS Google Scholar
Monot, M., Boursaux-Eude, C., Thibonnier, M., Vallenet, D., Moszer, I., Medigue, C., Martin-Verstraete, I. & Dupuy, B. (2011). J. Med. Microbiol. 60, 1193–1199. Web of Science CrossRef CAS PubMed Google Scholar
Montanier, C. Y., Correia, M. A. S., Flint, J. E., Zhu, Y., Basle, A., McKee, L. S., Prates, J. A. M., Polizzi, S. J., Coutinho, P. M., Lewis, R. J., Henrissat, B., Fontes, C. M. G. A. & Gilbert, H. J. (2011). J. Biol. Chem. 286, 22499–22509. Web of Science CrossRef CAS PubMed Google Scholar
Murshudov, G. N., Skubák, P., Lebedev, A. A., Pannu, N. S., Steiner, R. A., Nicholls, R. A., Winn, M. D., Long, F. & Vagin, A. A. (2011). Acta Cryst. D67, 355–367. Web of Science CrossRef CAS IUCr Journals Google Scholar
Nägler, D. K., Zhang, R., Tam, W., Sulea, T., Purisima, E. O. & Ménard, R. (1999). Biochemistry, 38, 12648–12654. Web of Science PubMed Google Scholar
Ness, S. R., de Graaff, R. A., Abrahams, J. P. & Pannu, N. S. (2004). Structure, 12, 1753–1761. Web of Science CrossRef PubMed CAS Google Scholar
Newstead, S. L., Watson, J. N., Bennet, A. J. & Taylor, G. (2005). Acta Cryst. D61, 1483–1491. Web of Science CrossRef CAS IUCr Journals Google Scholar
Pannu, N. S., McCoy, A. J. & Read, R. J. (2003). Acta Cryst. D59, 1801–1808. Web of Science CrossRef CAS IUCr Journals Google Scholar
Pannu, N. S. & Read, R. J. (2004). Acta Cryst. D60, 22–27. Web of Science CrossRef CAS IUCr Journals Google Scholar
Pruitt, R. N., Chagot, B., Cover, M., Chazin, W. J., Spiller, B. & Lacy, D. B. (2009). J. Biol. Chem. 284, 21934–21940. Web of Science CrossRef PubMed CAS Google Scholar
Rawlings, N. D., Barrett, A. J. & Bateman, A. (2010). Nucleic Acids Res. 38, D227–D233. Web of Science CrossRef PubMed CAS Google Scholar
Reynolds, C. B., Emerson, J. E., de la Riva, L., Fagan, R. P. & Fairweather, N. F. (2011). PLoS Pathog. 7, e1002024. Web of Science CrossRef PubMed Google Scholar
Riva, L. de la, Willing, S. E., Tate, E. W. & Fairweather, N. F. (2011). J. Bacteriol. 193, 3276–3285. Web of Science PubMed Google Scholar
Rupnik, M., Wilcox, M. H. & Gerding, D. N. (2009). Nature Rev. Microbiol. 7, 526–536. Web of Science CrossRef CAS Google Scholar
Sajid, M. & McKerrow, J. H. (2002). Mol. Biochem. Parasitol. 120, 1–21. Web of Science CrossRef PubMed CAS Google Scholar
Sampathkumar, P. et al. (2010). J. Mol. Biol. 397, 883–892. Web of Science CrossRef CAS PubMed Google Scholar
Sára, M., Dekitsch, C., Mayer, H. F., Egelseer, E. M. & Sleytr, U. B. (1998). J. Bacteriol. 180, 4146–4153. Web of Science PubMed Google Scholar
Sára, M. & Sleytr, U. B. (2000). J. Bacteriol. 182, 859–868. Web of Science CrossRef PubMed CAS Google Scholar
Savariau-Lacomme, M.-P., Lebarbier, C., Karjalainen, T., Collignon, A. & Janoir, C. (2003). J. Bacteriol. 185, 4461–4470. Web of Science PubMed CAS Google Scholar
Schechter, I. & Berger, A. (1967). Biochem. Biophys. Res. Commun. 27, 157–162. CrossRef CAS PubMed Web of Science Google Scholar
Sebaihia, M. et al. (2006). Nature Genet. 38, 779–786. Web of Science CrossRef PubMed Google Scholar
Shen, A., Lupardus, P. J., Gersch, M. M., Puri, A. W., Albrow, V. E., Garcia, K. C. & Bogyo, M. (2011). Nature Struct. Mol. Biol. 18, 364–371. Web of Science CrossRef CAS Google Scholar
Sivaraman, J., Lalumière, M., Ménard, R. & Cygler, M. (1999). Protein Sci. 8, 283–290. CrossRef PubMed CAS Google Scholar
Turk, D., Podobnik, M., Kuhelj, R., Dolinar, M. & Turk, V. (1996). FEBS Lett. 384, 211–214. CrossRef CAS PubMed Web of Science Google Scholar
Waligora, A. J., Hennequin, C., Mullany, P., Bourlioux, P., Collignon, A. & Karjalainen, T. (2001). Infect. Immun. 69, 2144–2153. Web of Science CrossRef PubMed CAS Google Scholar
Wiggers, H. J., Rocha, J. R., Fernandes, W. B., Sesti-Costa, R., Carneiro, Z. A., Cheleski, J., da Silva, A. B. F., Juliano, L., Cezari, M. H. S., Silva, J. S., McKerrow, J. H. & Montanari, C. A. (2013). PLoS Negl. Trop. Dis. 7, e2370. Web of Science CrossRef PubMed Google Scholar
Winn, M. D. et al. (2011). Acta Cryst. D67, 235–242. Web of Science CrossRef CAS IUCr Journals Google Scholar
Winter, G., Lobley, C. M. C. & Prince, S. M. (2013). Acta Cryst. D69, 1260–1273. Web of Science CrossRef CAS IUCr Journals Google Scholar
Wright, A., Drudy, D., Kyne, L., Brown, K. & Fairweather, N. F. (2008). J. Med. Microbiol. 57, 750–756. Web of Science CrossRef PubMed CAS Google Scholar
Zheng, H., Chruszcz, M., Lasota, P., Lebioda, L. & Minor, W. (2008). J. Inorg. Biochem. 102, 1765–1776. Web of Science CrossRef PubMed CAS Google Scholar
This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.