The complement component 5 (C5)-binding antibody eculizumab is used to treat patients with paroxysmal nocturnal hemoglobinuria (PNH) and atypical haemolytic uremic syndrome (aHUS). As recently reported there is a need for a precise classification of eculizumab responsive patients to allow for a safe and cost-effective treatment. To allow for such stratification, knowledge of the precise binding site of the drug on its target is crucial. Using a structural epitope mapping strategy based on bacterial surface display, flow cytometric sorting and validation via haemolytic activity testing, we identified six residues essential for binding of eculizumab to C5. This epitope co-localizes with the contact area recently identified by crystallography and includes positions in C5 mutated in non-responders. The identified epitope also includes residue W917, which is unique for human C5 and explains the observed lack of cross-reactivity for eculizumab with other primates. We could demonstrate that Ornithodorus moubata complement inhibitor (OmCI), in contrast to eculizumab, maintained anti-haemolytic function for mutations in any of the six epitope residues, thus representing a possible alternative treatment for patients non-responsive to eculizumab. The method for stratification of patients described here allows for precision medicine and should be applicable to several other diseases and therapeutics.
The term precision medicine describes the idea of providing effective treatment based on a patient’s molecular make up. Recent advances in molecular diagnostic tools and handling of large data sets allow for the stratification of patients based on e.g. genetic or protein information and make it possible to provide tailored treatment for these sub-groups1. Here we describe how epitope information, exemplified by binding of the therapeutic antibody eculizumab on its target complement component 5 (C5), can be used to guide treatment.
The complement system is an important part of the human innate immunity. It fulfils an important role in fighting bacterial infections and homeostasis and provides a link between innate and adaptive immune response2. Such powerful functions require a tight regulation to prevent the complement system from attacking the host’s cells. Paroxysmal nocturnal hemoglobinuria (PNH) and atypical haemolytic uremic syndrome (aHUS) are two disorders associated with a malfunctioning complement system. PNH is characterized by blood cells deficient of glycosylphosphatidylinositol (GPI)-anchored proteins, which protect cells from complement attack, caused by an acquired mutation in hematopoietic stem cells3,4,5. This consequently results in intravascular haemolysis, which in turn leads to anaemia and thrombosis4,5,6. Atypical HUS is a renal disease that is characterized by an unregulated activation of the alternative pathway of the complement resulting in thrombosis in kidney capillaries and renal failure7,8.
The monoclonal antibody eculizumab (Soliris®) is the first FDA-approved therapeutic antibody for treatment of PNH2,4,5,9 and aHUS7,10. Eculizumab is a humanized monoclonal antibody targeting C5. The suggested mode of action is that eculizumab binding to C5 prevents the entry and subsequent cleavage of C5 by C5 convertase7,11. C5 is a central protein in the complement system cascade that is common to all three pathways. This makes it attractive as a therapeutic target. By inhibiting C5 cleavage the common downstream cascade can be disrupted independent of the activating pathway, i.e. no C5b-9 formation (membrane attack complex, MAC) and generation of the anaphylatoxin C5a occurs2,5. At the same time, the upstream pathways resulting in generation of C3b are kept intact and thus pathogen clearance via C3b-mediated opsonisation is not impaired4,5. Besides the approved treatment of PNH and aHUS, eculizumab has also proven effective in some cases for treatment of other conditions, like myasthenia gravis12,13, neuromyelitis optica14,15, membranoproliferative glomerulonephritis16,17, catastrophic antiphospholipid syndrome18,19,20 and prevention of rejection after renal transplants21,22,23.
Despite the proven relevance of the drug, reports on non- or poorly responding patients have been published24,25,26,27,28. Among them a study on Japanese PNH patients which carried a mutation in the C5 gene, which changes the C5 protein so that it can no longer be bound by eculizumab24. This highlights the need for an exact determination of eculizumab’s epitope on C5. Such knowledge would enable the development of genotyping kits for the prediction of responsiveness of a patient to eculizumab treatment.
Different efforts have been undertaken to identify the binding site of eculizumab on C511,29,30. In an earlier report to the Japanese Pharmaceutical and Food Safety Bureau29, eculizumab was reported to have a conformational epitope consisting of three distant amino acid stretches covering residues 822 to 826 (DVFLE), 879 to 883 (KSSKC) and 930 to 933 (VPEG). Later, Zuber et al.7 only refer to KSSKC as eculizumab’s epitope. In a recent publication30 based on transmission electron microscopy (TEM), eculizumab was found to interact with the MG7 domain with R885 and the KSSKC peptide being part of the binding site. While the present study was under review the crystal structure of C5 in complex with the eculizumab Fab fragment was solved11. While accurately determining the region of binding, the resolution of the co-crystal structure did not allow an unambiguous determination of intermolecular interactions at residue level.
Here, we used an epitope mapping strategy based on deep mutational scanning of surface-displayed protein domains to explore in detail the structural epitope properties of eculizumab. While high-resolution X-ray crystallography of the antibody complex still represents the gold standard for epitope determination31 other epitope mapping methods have been developed, like peptide scanning32, alanine scanning33 and several combinatorial library techniques34 that are applicable to a wider range of proteins and offer higher throughput. The approach presented here is based on the gram-positive bacterium Staphylococcus carnosus (S. carnosus)35,36, which proved to be advantageous for display applications due to its high mechanical resistance allowing for cell sorting applications and the lack of extracellular proteolytic activity37,38. For the first time, staphylococcal display was used for mapping of a structural epitope by displaying randomly mutated protein domains on the surface of S. carnosus. The combination of random mutagenesis and surface display of protein domains allows a more thorough analysis of the mutational space under native-like conditions in contrast to other high-throughput mapping techniques like peptide arrays and alanine scanning.
The presented workflow (Fig. 1a) includes the identification of a binding domain, creation of a mutant display library, identification and sorting of surface expressed non-binding domain mutants using flow cytometry and sequencing of them. To confirm the identified positions the mutants were produced as full-length proteins in mammalian cells and functionally analysed for haemolytic activity and binding to the antibody. The identified C5 residues involved in the binding to eculizumab were matched against reported germline variations of relevance for the prediction of responders to treatment with this therapeutic antibody, which constitutes the stratification part of the workflow (Fig. 1b). Comparing the patient’s gene sequence with the epitope of available drugs enables stratification into treatment groups. Our work outlines a general strategy for stratification of responders and non-responders for treatment with therapeutic antibodies and more specifically analyses the underlying molecular mechanism for patients’ response to the therapeutic antibody eculizumab.
Eculizumab binds to MG7 domain displayed on Staphylococci
The complement factor C5 has been structurally characterized and found to consist of twelve domains39,40. Each of the twelve domains (colour coded in the Fig. 1a) was cloned and expressed using a Gram-positive bacterial surface expression system (Supplementary Fig. S1). This allowed binding analysis of the monoclonal antibody eculizumab using a fluorescently labelled secondary antibody and flow sorting of the resulting bacterial cells with the respective domains exposed on the surface (shown schematically in Fig. 1a). The binding analysis showed that the monoclonal antibody binds exclusively to the domain MG7 (residues 822–931) expressed on Staphylococci, while all other eleven domains were shown not to interact with the antibody (Fig. 1c).
Loss of binding mutations identified from random mutagenesis library
Having identified the MG7 domain as the binding domain for eculizumab, a random mutagenesis library of this domain was constructed by error-prone PCR (as shown schematically in Fig. 1a. The size of the staphylococcal library was 1.42 × 104 clones and sequencing of 96 randomly picked clones revealed a mutation frequency of 1.4 nucleotide mutations per gene (data not shown). The albumin-binding protein (ABP), expressed in fusion with the respective mutated domain before the membrane anchoring domain, was used with labelled human serum albumin (HSA) to detect surface expression of the domain. Mutations within MG7 leading to overall misfolding of the domain or introduction of stop codons were expected not to be secreted nor properly anchored to the cell surface34, resulting in a decrease or absence of ABP signal for these, making it possible to avoid these during flow sorting. Clones that showed a retained high HSA signal, but a reduction in eculizumab binding were sorted in two successive rounds of flow cytometric cell sorting as indicated in Fig. 1c. After cultivating this population of enriched mutants under selective conditions on an agar plate, colonies from the sorted pool were picked and subjected to sequence analysis and characterization. Out of 90 individual clones, 71 coded for unique protein sequences with the majority containing several amino acid mutations. To facilitate data analysis and in order to be able to draw unambiguous conclusions about the contribution of a residue to antibody binding, clones containing multiple amino acid mutations were excluded from the analysis. 15 clones were identified encoding for a single amino acid mutation (Supplementary Fig. S2). Mutations involving the amino acids cysteine, glycine and proline were omitted from the analysis due to the fact that such amino acid changes often result in disruption of the overall conformation34. One of the clones discarded due to the mutation coding for a cysteine (R885C) had earlier been reported as a mutation present in patients24 and was therefore included in the subsequent analysis. This resulted in the identification of 11 clones (I829K, Q854L, F855I, R885C, R885H, K887N, K887R, K887T, V896E, W917L, F918S) with a single mutation in the MG7 domain.
The 11 identified clones were analysed individually by flow cytometry for their binding to eculizumab. The analysis confirmed that they all had reduced binding to the monoclonal antibody compared to the wild type control (Fig. 2a). Some mutations, such as F918S and K887T, reduce the capability of binding to eculizumab, while others, such as Q854L, R885C/H and K887N, seem to eliminate binding completely. Interestingly, the three different mutations found at position 887 all showed reduced binding, but the degree of binding varied considerably depending on which amino acid it was changed to (asparagine, arginine or threonine). In summary, the results from the eleven clones suggest that eight different amino acids in the C5 domain are involved in the binding to the therapeutic antibody eculizumab.
Mammalian produced full-length C5 mutants show decrease in binding to eculizumab
The wild type C5 protein and nine mutants identified above including R885C and one of the K887 mutants (K887N) were expressed and purified from transiently transfected CHO cells. A C-terminal protein C peptide tag41 enabled efficient affinity purification using the HPC4 monoclonal antibody. After purification, the purified C5 proteins were analysed by SDS-PAGE (Supplementary Fig. S3). The protein gel displayed two clear bands of the alpha (104 kDa) and beta chain (73 kDa) confirming a proper maturation by specific protease cleavage of pro-C5. The ability to purify both chains using the C-terminal tag of the beta-chain indicates that the two fragments are covalently interacting through native cysteine bridge.
The nine mutant C5 proteins together with the wild type C5 were analysed for binding to eculizumab by sandwich ELISA. The analysis confirmed that many of the mutants, except I829K and V896E, showed reduced binding (Fig. 2b). Although the effect for F918S is relatively low and the decrease in binding for W917L is non-significant, we decided to analyse also these mutants further. Most dramatic effect in binding to eculizumab could be attributed to the R885 mutants with almost complete loss of reactivity in the ELISA assay.
Eculizumab cannot inhibit the haemolytic activity of the C5 mutants
The haemolytic activity, i.e. the ability to elicit C5b-9 formation, was analysed for the recombinant C5 variants that showed reduced binding to eculizumab in ELISA to exclude that the drop in binding is due to a major structural change brought about by the mutation. The analysis shows that all mutants are able to induce C5b-9 formation in a concentration-dependent manner (Fig. 3a), although some, like R885C, do this to a lower degree than wild type C5. The lower activity of W917L could be attributed to the fact that this residue is likely to be involved in convertase binding42. When adding 3.7 nM eculizumab to this activity test, C5b-9 formation was inhibited in wild type C5, while mutants Q854L, R885C, R885H and W917L showed a nearly unchanged activity and F855I, K887N and F918S displayed a clearly lowered eculizumab effect (Fig. 3b and Supplementary Fig. S4). The decreased effect of eculizumab on F855I is more distinct in Supplementary Fig. S4 showing that a higher amount of eculizumab is needed to inhibit F855I compared to WT C5. When 3 nM Ornithodorus moubata complement inhibitor (OmCI), a tick protein43,44 that does not compete with eculizumab for binding to C530, was added instead of eculizumab, C5b-9 formation was inhibited to the same degree as WT for all C5 variants (Fig. 3b,c for R885C). All analysed mutants showed a significantly reduced haemolysis when incubated with OmCI compared to eculizumab (Fig. 3b).
The six identified residues co-locate with the epitope regions identified by crystallography
The combined results from the binding and haemolysis experiments suggest that six residues are involved in binding to eculizumab, i.e. Q854, F855, R885, K887, W917 and F918. These residues are widely spread over the MG7 protein sequence (Fig. 4a) and therefore a structural analysis was done using the published co-crystal structure of C5 and an eculizumab Fab (PDB5I5K)11. The analysis showed that all six residues are brought together into a single site on the β-sheet in the folded C5 MG7 domain (Fig. 4b). All six residues fall into the three contact regions (residues 851–858, 882–888 and 915–920) identified by Schatz-Jakobsen et al.11 based on a less than 5 Å-distance to the Fab fragment. Further analysis revealed that, except for F855I, all five residues are more than 25% surface exposed (Fig. 4c) rendering them accessible for the antibody (Fig. 4d).
Naturally occurring germ line mutations of C5 located in epitope
To identify possible germ line mutations in the C5 gene, three different databases (NCBI dbSNP, 1000genomes and ExAC) were searched for missense mutations in MG7. Altogether 32 naturally occurring variations in the MG7 domain were found, listed in Table 1 together with the positions of the six identified epitope residues. Two of the mutations found to abolish binding of eculizumab to C5 (R885C and R885H) were found in the database query originating from a report24 on poor response to eculizumab in PNH patients. In addition several genetic variations were identified in close proximity to the suggested epitope and within the 5 Å region described above11, which could affect the binding of the drug to a lower degree.
W917 is specific for human C5 and is critical for eculizumab binding
It has been reported that eculizumab is specific for human C5 and that the lack of reactivity of orthologous C5 proteins has prohibited use of such animal models5. In Supplementary Fig. S5 the protein sequence for the epitope residues are aligned in nine different species, including primates, rat and mouse to try to explain this lack of binding. While F855 is completely conserved in all nine species, only the chemical properties of the residues at positions 887 and 918 are conserved. Residues Q854 and R885 are conserved between humans and primates, while W917 is unique for humans. All other analysed animals show a serine instead of tryptophan at position 917. Interestingly, analysis of the binding properties and haemolysis inhibition of a W917S mutant (Supplementary Fig. S6) demonstrates that this mutant has significantly decreased binding activity, thus explaining why eculizumab is non-functional in these animal models.
This work presents six residues on the complement protein C5 that are essential for the binding and function of the therapeutic antibody eculizumab and suggest that other means of treatment should be considered for individuals carrying mutations in these positions. All 12 domains of C5 were successfully expressed on the cell surface of S. carnosus and domain MG7 was identified as the binding domain of the therapeutic antibody eculizumab. A deep mutational scanning of MG7 was performed to determine the amino acids involved in eculizumab binding. After excluding multiple mutations and mutations to or from cysteine, glycine and proline that are likely to disrupt the protein structure34, eight residues were identified, which after functional analysis were condensed to six essential residues required for binding and function of the antibody. Although these residues are localized on different strands of the MG7 domain, they cluster to a single, contiguous site in the folded protein, suggesting that the epitope of eculizumab on C5 is dependent on tertiary structure.
This hypothesis was confirmed by the C5-eculizumab Fab co-crystal structure11 published after submission of this article. Schatz-Jakobsen et al. report three contact regions on C5 within the β-sheet of MG7 comprising residues 851–858, 882–888 and 915–920. Although the resolution of the crystallographic data did not allow the clear identification of single epitope residues, the authors inferred from the existence of binding pockets on the antibody that residues W917, F918 and R885 are involved in binding. All three residues could be confirmed to be essential for antibody binding by the surface display based epitope mapping approach presented here. In addition, three other residues, Q854, F885 and K887, which locate in the first and second contact region, described by Schatz-Jakobsen et al.11, respectively, were here shown to be important for eculizumab binding. Therefore, we regard the approach presented here using independently folded protein domains as a screening platform well suited for detection of contact residues in a structural context.
Our binding assays with full-length C5 variants from mammalian sources have shown that the findings about the eculizumab epitope on domain level on the staphylococcal surface are transferable and relevant for full-length human C5. Analysis of surface exposure reveals that all residues but F855 exceed 25% surface exposure. This might account for the lower degree of haemolytic activity, i.e. a higher degree of inhibition by eculizumab, observed for this mutant in the haemolysis inhibition assay (Fig. 3b). As Schatz-Jakobsen et al.11 we identified residue W917 as an important contact residue in this work. Our mutation studies confirmed the absence of eculizumab binding to a W917S C5 mutant. Sequence comparison showed that tryptophan at this position is specific for human C5. Considering that chimpanzee C5 only differs in two amino acids within the MG7 domain from human C5, W917 being one of them, these findings explain the species specificity observed for eculizumab, which is not able to bind to C5 of any other species but human5. Also R885’s involvement in eculizumab binding could be confirmed in this work. The crystal structure suggests that the mutated residues (His and Cys) are too small to fit the binding pocket11. Schatz-Jakobsen et al. also hypothesised that a cysteine mutation at that position could affect the disulphide bridge between residues 856 and 883. We observed a decreased haemolytic activity for the R885C mutant which could be explained by a structural change in the MG7 domain that perturbs interaction of this domain with the convertase42.
The clinical relevance of R885-mutations is highlighted by a study on Japanese PNH patients24 exhibiting poor response to eculizumab. Considering these insights from R885 mutation on eculizumab response, the same is thought to be true for any of the other residues found in this work to be involved in eculizumab binding. Although no germline mutations are reported for these five residues today, mutations have been reported for residues in close proximity to eculizumab as determined by the crystal structure11. Also mutations at these positions are likely to impair the responsiveness to eculizumab. But an analysis of single mutants would be needed to verify this. As shown in the haemolysis inhibition analysis patients with a mutation at F855, K887 and F918 would need a higher dose of eculizumab to elicit the same response as with non-mutant C5, while patients carrying a mutation at Q854, R885 and W917 likely respond so poorly to eculizumab treatment that an alternative treatment should be considered. Consequently, a clearly defined epitope as presented here can prove helpful in the clinics to screen for patients’ susceptibility to eculizumab treatment and allows for a more effective treatment.
Moreover, it could be shown that the C5 complement inhibitor OmCI, which binds at a site distinct from eculizumab30, was, in contrast to eculizumab, able to completely prevent the haemolysis induced by the mutant C5 molecules. Considering that OmCI, also known as coversin, was earlier reported as a possible therapeutic30,45,46,47,48 with low immunogenicity45 and is currently undergoing clinical trial and given the results presented here, OmCI could represent an alternative future treatment strategy for patients responding poorly to eculizumab due to a missense mutation in eculizumab’s epitope on C5. Taken together our work outlines a general strategy for precision medicine based on detailed epitope mapping and genetic profiling, which should be transferable to several other diseases and therapies and which would allow for correct treatment on those who will benefit while sparing expense and side effects for non-responders.
Materials and Methods
Construction of the epitope mapping library and expression in S. carnosus
The mRNA sequence for C5 was obtained from Source BioScience (Cambridge, UK). The C5 domains according to Fredslund et al.40 were amplified by PCR and cloned into the staphylococcal display vector pSCEM238 (Supplementary Fig. 1) Transformation and library construction in S. carnosus is achieved as described before49. Briefly, the display vector pSCEM2 was amplified in E. coli and purified prior to transformation of S. carnosus TM 300 cells (a kind gift from Prof. F. Götz, University of Tübingen, Tübingen, Germany). S. carnosus cells were transformed by electroporation using a Bio-Rad MicroPulser electroporator at 2.3 kV for 1.1 ms. Transformed cells were grown at 37 °C overnight for protein surface expression. Having identified the C5 MG7 domain as binding domain of eculizumab (produced from CHO cells at Swedish Orphan Biovitrum AB (Sobi), Stockholm, Sweden, M.M.B, Chao Su, Lotta Berghard, Göran Selén, Kerstin Larsson, Joakim Nilsson, Catharina Sterky, Carina Ekholm, Per-Olof Edlund, Charlotte Söderberg Nyhem, P.S., manuscript in preparation), the domain was amplified using a Genemorph random mutagenesis kit (Agilent Technologies, Santa Clara, CA, USA) to yield an average mutation frequency of 1.4 mutations per sequence. The vector was purified by phenol chloroform extraction and cloned into S. carnosus as described above.
Antibody labelling and analysis by flow cytometry
Of an S. carnosus overnight culture 2 μL were taken for analysis. The cells were washed twice with phosphate buffered saline containing 0.1% pluronic (BASF, Ludwigshafen, Germany) (PBS-P) before incubation with eculizumab (8.8 nM) for 45 min at room temperature. The cells were then washed with PBS-P and incubated with Alexa 488-labeled goat-anti-human secondary antibody (2 μg/mL) and Alexa 647-labeled HSA (1:1000 dilution) for expression control on ice in the dark for 30 min. After a final washing step the cells expressing the protein domains were analysed in a Gallios flow cytometer (Beckman Coulter, Brea, CA, USA). The same protocol was also applied when analysing the identified library clones individually.
Sorting of the random mutagenesis library
The library clones were labelled in the same way as described above. The cells were analysed and sorted in a MoFlo Astrios cell sorter (Beckman Coulter, Brea, CA, USA). The library was sorted for binding escape mutants that show a pertained high surface expression signal but a decreased antibody-binding signal. Two rounds of sorting for binding escape mutants were performed with the sorting gates indicated in Fig. 1c to reduce the risk for false positive clones. The sorted cells were incubated on agar plates and 128 clones picked for sequence analysis.
Production of soluble C5 variants in mammalian cells
The gene for human C5 was cloned into vector pQMCF1 coding for full-length C5 protein C-terminally fused to a tobacco etch virus-protease site and a Human protein C epitope tag (HPC4). C5 mutants were derived from this plasmid by using the Q5® Site-Directed Mutagenesis Kit (New England Biolabs, Ipswich, MA, USA). Successful mutagenesis was confirmed by Sanger sequencing. Recombinant wildtype and mutant C5 was expressed in Chinese hamster ovary (CHO) EBNALT 85 cells (Icosagen, Tartu, Estonia) following the manufacturer’s guidelines for extended transient expression. After 15 days of cultivation C5 proteins were purified from the cell culture supernatant by affinity chromatography on an anti-protein C affinity matrix (Roche, Basel, Switzerland). Due to low protein concentration, some samples were concentrated using a centrifugal filter (Merck Millipore, Darmstadt, Germany). Protein concentration was determined with ImageJ (see supplementary methods) from a Coomassie-stained sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) (Supplementary Fig. S3). All non-concentrated protein samples had a purity of over 95% as assessed by Coomassie staining after SDS-PAGE (Supplementary Fig. S3).
Binding analysis of full-length, soluble C5 variants
Binding of recombinant wildtype and mutant C5 was assessed by ELISA. A 96-well half area plate was coated overnight with 33.3 nM OmCI (produced at Sobi as described in Bloom et al.50). The next day, the plate was blocked with PBS containing 1% bovine serum albumin (BSA). C5 variants were added at a concentration of 63 nM in blocking buffer. After washing the plate, eculizumab was added at a concentration of 16 nM. Antibody binding was detected with help of an anti-human IgG antibody coupled to horseradish peroxidase (HRP) and Tetramethylbenzidine (TMB) substrate. The reaction was terminated by addition of 2 M sulfuric acid. Absorbance was measured at 450 nm.
Activity analysis of full-length, soluble C5 variants
The ability of WT and mutated C5 to form C5b-9 was monitored by haemolytic activity using antibody (Rabbit anti-sheep RBC stroma, Sigma #S1389) coated sheep red blood cells. 5 × 106 cells in 50 μL GVBp (0.15 mM CaCl2, 0.5 mM MgCl2, 3 mM NaN3, 138 mM NaCl, 0.1% gelatine, 1.8 mM sodium barbital and 3.1 mM barbituric acid, pH 7.3–7.4) were used and the amount of hemolysis was monitored as absorbance at 415 nm. Diluted C5 deficient human serum (1:50) was spiked with C5 (WT or mutant) at different concentrations ranging from 51.2 nM to 6.25 pM. Subsequently, the capacity to inhibit haemolytic activity by eculizumab and OmCI at 100–0.001 nM was monitored using C5 concentrations optimized to normalize haemolytic activity between C5 variants; 0.023 nM (WT), 0.013 nM (Q854L), 0.011 nM (F855I), 8.9 nM (R885C), 0.089 nM (R885H), 0.046 nM (K887N), 0.72 nM (W917L), 1.6 nM (W917S) and 0.089 nM (F918S).
The six identified amino acid mutations were visualized on an existing 3D structure of C5 (PDB5I5K)11 using ICM software (Molsoft LLC, San Diego, USA). For comparison of the six identified residues with naturally occurring germ line mutations, three databases, dbSNP51, 1000genomes52 and the Exome Aggregation Consortium (ExAC) browser53, were searched for missense mutations occurring in the MG7 coding region (residues 822–931). Furthermore, the protein sequence of human C5 was aligned to C5 sequences of chimpanzee (Pan troglodytes), crab-eating macaque (Macaca fascicularis), rhesus macaque (Macaca mulatta), cat (Felis catus), wild boar (Sus scrofa), cow (Bos taurus), rat (Rattus norvegicus) and mouse (Mus musculus). The amino acids at the six identified positions were analysed for species conservation.
The mean of duplicates or triplicates is depicted in all column charts. Error bars indicate standard deviation. Statistical significance was calculated using GraphPad Prism Software. One-way Analysis of variance (ANOVA) with Dunnett’s multiple comparison test and two-way ANOVA with Tukey multiple comparison test was applied for ELISA results and haemolytic activity testing, respectively.
How to cite this article: Volk, A.-L. et al. Stratification of responders towards Eculizumab using a structural epitope mapping strategy. Sci. Rep. 6, 31365; doi: 10.1038/srep31365 (2016).
Collins, F. S. & Varmus, H. A New Initiative on Precision Medicine. N. Engl. J. Med. 372, 793–795 (2015).
Ricklin, D. & Lambris, J. D. Complement-targeted therapeutics. Nat. Biotechnol. 25, 1265–75 (2007).
Bessler, M. et al. Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene. EMBO J 13, 110–7 (1994).
Hillmen, P. et al. Effect of Eculizumab on Hemolysis and Transfusion Requirements in Patients with Paroxysmal Nocturnal Hemoglobinuria. N. Engl. J. Med. 350, 552–559 (2004).
Rother, R. P., Rollins, S. A., Mojcik, C. F., Brodsky, R. A. & Bell, L. Discovery and development of the complement inhibitor eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria. Nat. Biotechnol. 25, 1256–64 (2007).
Hillmen, P., Lewis, S. M., Bessler, M., Luzzatto, L. & Dacie, J. V. Natural history of paroxysmal nocturnal hemoglobinuria. N. Engl. J. Med. 333, 1253–8 (1995).
Zuber, J., Fakhouri, F., Roumenina, L. T., Loirat, C. & Frémeaux-Bacchi, V. Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies. Nat. Rev. Nephrol. 8, 643–57 (2012).
Kavanagh, D., Goodship, T. H. & Richards, A. Atypical hemolytic uremic syndrome. Semin. Nephrol. 33, 508–30 (2013).
Dmytrijuk, A. et al. FDA report: eculizumab (Soliris) for the treatment of patients with paroxysmal nocturnal hemoglobinuria. Oncologist 13, 993–1000 (2008).
Schmidtko, J., Peine, S., El-Housseini, Y., Pascual, M. & Meier, P. Treatment of atypical hemolytic uremic syndrome and thrombotic microangiopathies: a focus on eculizumab. Am. J. Kidney Dis. 61, 289–99 (2013).
Schatz-Jakobsen, J. A. et al. Structural Basis for Eculizumab-Mediated Inhibition of the Complement Terminal Pathway. J. Immunol. doi: 10.4049/jimmunol.1600280 (2016).
Howard, J. F. et al. A randomized, double-blind, placebo-controlled phase II study of eculizumab in patients with refractory generalized myasthenia gravis. Muscle Nerve 48, 76–84 (2013).
Silvestri, N. J. & Wolfe, G. I. Treatment-refractory myasthenia gravis. J. Clin. Neuromuscul. Dis. 15, 167–78 (2014).
Pittock, S. J. et al. Eculizumab in AQP4-IgG-positive relapsing neuromyelitis optica spectrum disorders: an open-label pilot study. Lancet Neurol. 12, 554–562 (2013).
Kleiter, I. & Gold, R. Present and Future Therapies in Neuromyelitis Optica Spectrum Disorders. Neurotherapeutics 13, 70–83 (2016).
Radhakrishnan, S. et al. Eculizumab and Refractory Membranoproliferative Glomerulonephritis. N. Engl. J. Med. 366, 1165–1166 (2012).
Riedl, M., Thorner, P. & Licht, C. C3 Glomerulopathy. Pediatr. Nephrol. 1–15, doi: 10.1007/s00467-015-3310-4 (2016).
Shapira, I., Andrade, D., Allen, S. L. & Salmon, J. E. Brief report: induction of sustained remission in recurrent catastrophic antiphospholipid syndrome via inhibition of terminal complement with eculizumab. Arthritis Rheum. 64, 2719–23 (2012).
Lonze, B. E. et al. Eculizumab Prevents Recurrent Antiphospholipid Antibody Syndrome and Enables Successful Renal Transplantation. Am. J. Transplant. 14, 459–465 (2014).
Wig, S., Chan, M., Thachil, J., Bruce, I. & Barnes, T. A case of relapsing and refractory catastrophic anti-phospholipid syndrome successfully managed with eculizumab, a complement 5 inhibitor. Rheumatology 55, 382–384 (2016).
Legendre, C. et al. Eculizumab in renal transplantation. Transplant. Rev. 27, 90–92 (2013).
Johnson, C. K. & Leca, N. Eculizumab use in kidney transplantation. Curr. Opin. Organ Transplant. 20, 643–51 (2015).
Cornell, L. D., Schinstock, C. A., Gandhi, M. J., Kremers, W. K. & Stegall, M. D. Positive Crossmatch Kidney Transplant Recipients Treated With Eculizumab: Outcomes Beyond 1 Year. Am. J. Transplant. 15, 1293–1302 (2015).
Nishimura, J. et al. Genetic variants in C5 and poor response to eculizumab. N. Engl. J. Med. 370, 632–9 (2014).
DeZern, A. E., Dorr, D. & Brodsky, R. A. Predictors of hemoglobin response to eculizumab therapy in paroxysmal nocturnal hemoglobinuria. Eur. J. Haematol. 90, 16–24 (2013).
Stegall, M. D. et al. Terminal complement inhibition decreases antibody-mediated rejection in sensitized renal transplant recipients. Am. J. Transplant 11, 2405–13 (2011).
Burbach, M. et al. Report of the Inefficacy of Eculizumab in Two Cases of Severe Antibody-Mediated Rejection of Renal Grafts. Transplantation 98, 1056–1059 (2014).
Cornec-Le Gall, E. et al. Adult-onset eculizumab-resistant hemolytic uremic syndrome associated with cobalamin C deficiency. Am. J. Kidney Dis. 63, 119–23 (2014).
Evaluation and Licensing Division, Pharmaceutical and Food Safety Bureau Ministry of Health, Labour and Welfare. Report on the Deliberation Results. https://www.pmda.go.jp/files/000153009.pdf (2010).
Jore, M. M. et al. Structural basis for therapeutic inhibition of complement C5. Nat. Struct. Mol. Biol. 23, 378–386 (2016).
Gershoni, J. M., Roitburd-Berman, A., Siman-Tov, D. D., Tarnovitski Freund, N. & Weiss, Y. Epitope mapping: the first step in developing epitope-based vaccines. BioDrugs 21, 145–56 (2007).
Geysen, H. M., Meloen, R. H. & Barteling, S. J. Use of peptide synthesis to probe viral antigens for epitopes to a resolution of a single amino acid. Proc. Natl. Acad. Sci. USA 81, 3998–4002 (1984).
Cunningham, B. & Wells, J. High-resolution epitope mapping of hGH-receptor interactions by alanine-scanning mutagenesis. Science 244, 1081–1085 (1989).
Chao, G., Cochran, J. R. & Wittrup, K. D. Fine epitope mapping of anti-epidermal growth factor receptor antibodies through random mutagenesis and yeast surface display. J. Mol. Biol. 342, 539–50 (2004).
Rockberg, J., Löfblom, J., Hjelm, B., Uhlén, M. & Ståhl, S. Epitope mapping of antibodies using bacterial surface display. Nat. Methods 5, 1039–45 (2008).
Rockberg, J., Löfblom, J., Hjelm, B., Ståhl, S. & Uhlén, M. Epitope mapping using gram-positive surface display. Curr. Protoc. Immunol. Chapter 9, Unit9.9 (2010).
Samuelson, P. et al. Cell surface display of recombinant proteins on Staphylococcus carnosus. J. Bacteriol. 177, 1470–6 (1995).
Hudson, E. P., Uhlen, M. & Rockberg, J. Multiplex epitope mapping using bacterial surface display reveals both linear and conformational epitopes. Sci. Rep. 2, 706 (2012).
S. Laursen, N., Magnani, F., H. Gottfredsen, R., V. Petersen, S. & R. Andersen, G. Structure, Function and Control of Complement C5 and its Proteolytic Fragments. Curr. Mol. Med. 12, 1083–1097 (2012).
Fredslund, F. et al. Structure of and influence of a tick complement inhibitor on human complement component 5. Nat. Immunol. 9, 753–760 (2008).
Stearns, D. J., Kurosawa, S., Sims, P. J., Esmon, N. L. & Esmon, C. T. The interaction of a Ca2+ -dependent monoclonal antibody with the protein C activation peptide region. Evidence for obligatory Ca2+ binding to both antigen and antibody. J. Biol. Chem. 263, 826–32 (1988).
Laursen, N. S. et al. Substrate recognition by complement convertases revealed in the C5-cobra venom factor complex. Eur. Mol. Biol. Organ. J 30, 606–616 (2011).
Roversi, P. et al. The structure of OMCI, a novel lipocalin inhibitor of the complement system. J. Mol. Biol. 369, 784–93 (2007).
Nunn, M. A. et al. Complement Inhibitor of C5 Activation from the Soft Tick Ornithodoros moubata. J. Immunol. 174, 2084–2091 (2005).
Hepburn, N. J. et al. In vivo characterization and therapeutic efficacy of a C5-specific inhibitor from the soft tick Ornithodoros moubata. J. Biol. Chem. 282, 8292–9 (2007).
Barratt-Due, A. et al. Ornithodoros moubata complement inhibitor is an equally effective C5 inhibitor in pigs and humans. J. Immunol. 187, 4913–9 (2011).
Ricklin, D. & Lambris, J. D. Progress and trends in complement therapeutics. Adv. Exp. Med. Biol. 735, 1–22 (2013).
Ueda Y. et al. Coversin Blocked in Vitro Hemolysis in an Eculizumab-Resistant PNH Patient with the C5 Polymorphism (c.2654G>A). https://ash.confex.com/ash/2015/webprogram/Paper79479.html (2015).
Volk, A.-L., Hu, F. J. & Rockberg, J. Epitope mapping of monoclonal and polyclonal antibodies using bacterial cell surface display. Methods Mol. Biol. 1131, 485–500 (2014).
Blom, A. M. et al. A novel method for direct measurement of complement convertases activity in human serum. Clin. Exp. Immunol. 178, 142–53 (2014).
Sherry, S. T. et al. dbSNP: the NCBI database of genetic variation. Nucleic Acids Res. 29, 308–11 (2001).
Abecasis, G. R. et al. An integrated map of genetic variation from 1,092 human genomes. Nature 491, 56–65 (2012).
Exome Aggregation Consortium (ExAC), Cambridge, MA. http://exac.broadinstitute.org (2014).
This work was supported by the ProNova Centre for Protein Technology, the Novo Nordisk Foundation Center for Biosustainability at the Technical University of Denmark, Wallenberg Center for Protein Research and the Human Protein Atlas. The Erling-Persson Family Foundation is acknowledged for financial support of the KTH Center for Applied Proteomics.
The authors declare no competing financial interests.
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Volk, A., Hu, F., Berglund, M. et al. Stratification of responders towards eculizumab using a structural epitope mapping strategy. Sci Rep 6, 31365 (2016) doi:10.1038/srep31365
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