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5DYO

Fab43.1 complex with flourescein

5DYO の概要
エントリーDOI10.2210/pdb5dyo/pdb
分子名称Fab 43.1 Heavy Chain, Fab 43.1 Light Chain, 2-(6-HYDROXY-3-OXO-3H-XANTHEN-9-YL)-BENZOIC ACID, ... (5 entities in total)
機能のキーワードantibody fab flourescein, immune system
由来する生物種Mus musculus
詳細
タンパク質・核酸の鎖数4
化学式量合計94662.89
構造登録者
Longenecker, K.L.,Judge, R.A. (登録日: 2015-09-25, 公開日: 2016-01-27, 最終更新日: 2024-10-30)
主引用文献Gayda, S.,Longenecker, K.L.,Judge, R.A.,Swift, K.M.,Manoj, S.,Linthicum, D.S.,Tetin, S.Y.
Three-dimensional structure, binding, and spectroscopic characteristics of the monoclonal antibody 43.1 directed to the carboxyphenyl moiety of fluorescein.
Biopolymers, 105:234-243, 2016
Cited by
PubMed Abstract: Unlike other known anti-fluorescein antibodies, the monoclonal antibody 43.1 is directed toward the fluorescein's carboxyl phenyl moiety. It demonstrates a very high affinity (KD ∼ 70 pM) and a fast association rate (kon ∼ 2 × 10(7) M(-1 ) s(-1) ). The three-dimensional structure of the Fab 43.1-fluorescein complex was resolved at 2.4 Å resolution. The antibody binding site is exclusively assembled by the CDR loops. It is comprised of a 14 Å groove-shaped entrance leading to a 9 Å by 7 Å binding pocket. The highly polar binding pocket complementary encloses the fluorescein's carboxyphenyl moiety and tightly fixes it by multiple hydrogen bonds. The fluorescein's xanthene ring is embedded in the more hydrophobic groove and stacked between the side chains of Tyr37L and of Arg99H providing conditions for an excited state electron transfer process. In comparison to fluorescein, the absorption spectrum of the complex in the visible region is shifted to the "red" by 23 nm. The complex demonstrates a very weak fluorescence (Φc  = 0.0018) with two short lifetime components: 0.03 ns (47%) and 0.8 ns (24%), which reflects a 99.8% fluorescein emission quenching effect upon complex formation. The antibody 43.1 binds fluorescein with remarkable affinity, fast association rate, and strongly quenches its emission. Therefore, it may present a practical interest in applications such as molecular sensors and switches.
PubMed: 26756394
DOI: 10.1002/bip.22801
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.36 Å)
構造検証レポート
Validation report summary of 5dyo
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2025-12-24に公開中

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