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6D0X

Crystal structure of chimeric H.2140 / K.1210 Fab in complex with circumsporozoite protein NANP3

6D0X の概要
エントリーDOI10.2210/pdb6d0x/pdb
関連するPDBエントリー6D01
分子名称2140 Antibody, heavy chain, 1210 Antibody, light chain, NANP3, ... (6 entities in total)
機能のキーワードmalaria, antibody, circumsporozoite protein, immune system
由来する生物種Homo sapiens (Human)
詳細
タンパク質・核酸の鎖数3
化学式量合計49260.71
構造登録者
Scally, S.W.,Bosch, A.,Imkeller, K.,Wardemann, H.,Julien, J.P. (登録日: 2018-04-11, 公開日: 2018-06-13, 最終更新日: 2024-10-09)
主引用文献Imkeller, K.,Scally, S.W.,Bosch, A.,Marti, G.P.,Costa, G.,Triller, G.,Murugan, R.,Renna, V.,Jumaa, H.,Kremsner, P.G.,Sim, B.K.L.,Hoffman, S.L.,Mordmuller, B.,Levashina, E.A.,Julien, J.P.,Wardemann, H.
Antihomotypic affinity maturation improves human B cell responses against a repetitive epitope.
Science, 360:1358-1362, 2018
Cited by
PubMed Abstract: Affinity maturation selects B cells expressing somatically mutated antibody variants with improved antigen-binding properties to protect from invading pathogens. We determined the molecular mechanism underlying the clonal selection and affinity maturation of human B cells expressing protective antibodies against the circumsporozoite protein of the malaria parasite (PfCSP). We show in molecular detail that the repetitive nature of PfCSP facilitates direct homotypic interactions between two PfCSP repeat-bound monoclonal antibodies, thereby improving antigen affinity and B cell activation. These data provide a mechanistic explanation for the strong selection of somatic mutations that mediate homotypic antibody interactions after repeated parasite exposure in humans. Our findings demonstrate a different mode of antigen-mediated affinity maturation to improve antibody responses to PfCSP and presumably other repetitive antigens.
PubMed: 29880723
DOI: 10.1126/science.aar5304
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.849 Å)
構造検証レポート
Validation report summary of 6d0x
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-15に公開中

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