2BRR

Complex of the neisserial PorA P1.4 epitope peptide and two Fab- fragments (antibody MN20B9.34)

2BRR の概要

• エントリーDOI: 10.2210/pdb2brr/pdb
• 分子名称: MN20B9.34 ANTI-P1.4 ANTIBODY, FAB HEAVY CHAIN, MN20B9.34 ANTI-P1.4 ANTIBODY, FAB LIGHT CHAIN, CLASS 1 OUTER MEMBRANE PROTEIN VARIABLE REGION 2, ... (6 entities in total)
• 機能のキーワード: immune system, fab fragment, anti-pora antibody, p1.4 antibody, antigen, porin, transmembrane, antibody-antigen complex
• 由来する生物種: MUS MUSCULUS (HOUSE MOUSE); 詳細
• タンパク質・核酸の鎖数: 5
• 化学式量合計: 97058.22

構造登録者

Oomen, C.J.,Hoogerhout, P.,Kuipers, B.,Vidarsson, G.,Van Alphen, L.,Gros, P. (登録日: 2005-05-11, 公開日: 2005-07-27, 最終更新日: 2024-11-20)

主引用文献

Oomen, C.J.,Hoogerhout, P.,Kuipers, B.,Vidarsson, G.,Van Alphen, L.,Gros, P.
Crystal Structure of an Anti-Meningococcal Subtype P1.4 Pora Antibody Provides Basis for Peptide- Vaccine Design.
J.Mol.Biol., 351:1070-, 2005

PubMed Abstract: In various western countries, subtype P1.4 of Neisseria meningitidis serogroup B causes the greatest incidence of meningococcal disease. To investigate the molecular recognition of this subtype, we crystallised a peptide (P1HVVVNNKVATH(P11)), corresponding to the subtype P1.4 epitope sequence of outer membrane protein PorA, in complex with a Fab fragment of the bactericidal antibody MN20B9.34 directed against this epitope. Structure determination at 1.95 A resolution revealed a unique complex of one P1.4 antigen peptide bound to two identical Fab fragments. One Fab recognises the putative epitope residues in a 2:2 type I beta-turn at residues P5NNKV(P8), whereas the other Fab binds the C-terminal residues of the peptide that we consider a crystallisation artefact. Interestingly, recognition of the P1.4 epitope peptide is mediated almost exclusively through the complementarity-determining regions of the heavy chain. We exploited the observed turn conformation for designing conformationally restricted cyclic peptides for use as a peptide vaccine. The conformational stability of the two peptide designs was assessed by molecular dynamics simulations. Unlike the linear peptide, both cyclic peptides, conjugated to tetanus toxoid as a carrier protein, elicited antibody responses in mice that recognised meningococci of subtype P1.7-2,4. Serum bactericidal assays showed that some, but not all, of the sera induced with the cyclic peptide conjugates could activate the complement system with titres that were very high compared to the titres induced by complete PorA protein in its native conformation administered in outer membrane vesicles.

PubMed: 16038932
DOI: 10.1016/J.JMB.2005.06.061

実験手法

X-RAY DIFFRACTION (1.95 Å)