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5ADP

Crystal structure of the A.17 antibody FAB fragment - Light chain S35R mutant

5ADP の概要
エントリーDOI10.2210/pdb5adp/pdb
関連するPDBエントリー5ADO
分子名称FAB A.17 (3 entities in total)
機能のキーワードimmune system, enzyme reprogramming, antibodies, ig superfamily, in silico antibody maturation
由来する生物種HOMO SAPIENS (HUMAN)
詳細
タンパク質・核酸の鎖数2
化学式量合計54077.62
構造登録者
主引用文献Smirnov, I.V.,Golovin, A.V.,Chatziefthimiou, S.D.,Stepanova, A.V.,Peng, Y.,Zolotareva, O.I.,Belogurov, A.A.,Kurkova, I.N.,Ponomarenko, N.A.,Wilmanns, M.,Blackburn, G.M.,Gabibov, A.G.,Lerner, R.A.
Robotic Qm/Mm-Driven Maturation of Antibody Combining Sites.
Sci.Adv., 2:01695-, 2016
Cited by
PubMed Abstract: In vitro selection of antibodies from large repertoires of immunoglobulin (Ig) combining sites using combinatorial libraries is a powerful tool, with great potential for generating in vivo scavengers for toxins. However, addition of a maturation function is necessary to enable these selected antibodies to more closely mimic the full mammalian immune response. We approached this goal using quantum mechanics/molecular mechanics (QM/MM) calculations to achieve maturation in silico. We preselected A17, an Ig template, from a naïve library for its ability to disarm a toxic pesticide related to organophosphorus nerve agents. Virtual screening of 167,538 robotically generated mutants identified an optimum single point mutation, which experimentally boosted wild-type Ig scavenger performance by 170-fold. We validated the QM/MM predictions via kinetic analysis and crystal structures of mutant apo-A17 and covalently modified Ig, thereby identifying the displacement of one water molecule by an arginine as delivering this catalysis.
PubMed: 27774510
DOI: 10.1126/SCIADV.1501695
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.13 Å)
構造検証レポート
Validation report summary of 5adp
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2025-12-31に公開中

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