Two monoclonal antibodies to precisely the same epitope of type ii collagen select non-crossreactive phage clones by phage display: Implications for autoimmunity and molecular mimicry
Xu, Yuekang, Ramsland, Paul A., Davies, Janet M., Scealy, Marita, Nandakumar, Kutty Selva, Holmdahl, Rikard, & Rowley, Merrill J. (2004) Two monoclonal antibodies to precisely the same epitope of type ii collagen select non-crossreactive phage clones by phage display: Implications for autoimmunity and molecular mimicry. Molecular Immunology, 41(4), pp. 411-419.
Two monoclonal antibodies (mAb) CB268 and CII-C1 to type II collagen (CII) react with precisely the same conformational epitope constituted by the residues ARGLT on the three chains of the CII triple helix. The antibodies share structural similarity, with most differences in the complementarity determining region 3 of the heavy chain (HCDR3). The fine reactivity of these mAbs was investigated by screening two nonameric phage-displayed random peptide libraries. For each mAb, there were phage clones (phagotopes) that reacted strongly by ELISA only with the selecting mAb, and inhibited binding to CII only for that mAb, not the alternate mAb. Nonetheless, a synthetic peptide RRLPFGSQM corresponding to an insert from a highly reactive CII-C1-selected phagotope, which was unreactive (and non-inhibitory) with CB268, inhibited the reactivity of CB268 with CII. Most phage-displayed peptides contained a motif in the first part of the molecule that consisted of two basic residues adjacent to at least one hydrophobic residue (e.g. RRL or LRR), but the second portion of the peptides differed for the two mAbs. We predict that conserved CDR sequences interact with the basic-basic-hydrophobic motif, whereas non-conserved amino acids in the binding sites (especially HCDR3) interact with unique peptide sequences and limit cross-reactivity. The observation that two mAbs can react identically with a single epitope on one antigen (CII), but show no cross-reactivity when tested against a second (phagotope) indicates that microorganisms could exhibit mimics capable of initiating autoimmunity without this being evident from conventional assays.
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|Item Type:||Journal Article|
|Keywords:||2, 2′-azino-di-[3-ethylbenzthiazoline sulfonic acid]diammonium salt, aa, ABTS, amino acids, C1, CIA, CII, collagen-induced arthritis, ELISA, enzyme linked immunosorbent assay, HCDR, mAb, major epitope on CII, monoclonal antibody, type II collagen, amino acid, collagen antibody, collagen type 2, epitope, monoclonal antibody CB268, monoclonal antibody CII C1, peptide library, unclassified drug, amino acid analysis, amino acid sequence, article, autoimmunity, binding site, clone, cross reaction, molecular mimicry, molecule, phage display, priority journal, protein motif, screening, Amino Acid Motifs, Animals, Antibodies, Monoclonal, Antibody Specificity, Binding Sites, Antibody, Binding, Competitive, Cattle, Collagen Type II, Consensus Sequence, Cross Reactions, Crystallography, X-Ray, Enzyme-Linked Immunosorbent Assay, Epitopes, Hydrophobicity, Mice, Mice, Inbred DBA, Models, Molecular, Molecular Sequence Data, Protein Conformation|
|Copyright Owner:||Copyright 2004 Pergamon Press|
|Deposited On:||01 Oct 2015 04:44|
|Last Modified:||01 Oct 2015 04:44|
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