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7MDU

BG505 SOSIP MD39 in complex with the monoclonal antibodies Rh.33104 mAb.1 and RM20A3

7MDU の概要
エントリーDOI10.2210/pdb7mdu/pdb
EMDBエントリー23778 23779 23780
分子名称Rh.33104 mAb.1 Heavy Chain, Surface protein gp120, RM20A3 mAb Heavy Chain, ... (9 entities in total)
機能のキーワードmonoclonal antibody, immune complex, viral protein
由来する生物種Macaca mulatta
詳細
タンパク質・核酸の鎖数6
化学式量合計130957.74
構造登録者
Antanasijevic, A.,Ward, A.B. (登録日: 2021-04-06, 公開日: 2022-01-26, 最終更新日: 2024-11-06)
主引用文献Antanasijevic, A.,Bowman, C.A.,Kirchdoerfer, R.N.,Cottrell, C.A.,Ozorowski, G.,Upadhyay, A.A.,Cirelli, K.M.,Carnathan, D.G.,Enemuo, C.A.,Sewall, L.M.,Nogal, B.,Zhao, F.,Groschel, B.,Schief, W.R.,Sok, D.,Silvestri, G.,Crotty, S.,Bosinger, S.E.,Ward, A.B.
From structure to sequence: Antibody discovery using cryoEM.
Sci Adv, 8:eabk2039-eabk2039, 2022
Cited by
PubMed Abstract: One of the rate-limiting steps in analyzing immune responses to vaccines or infections is the isolation and characterization of monoclonal antibodies. Here, we present a hybrid structural and bioinformatic approach to directly assign the heavy and light chains, identify complementarity-determining regions, and discover sequences from cryoEM density maps of serum-derived polyclonal antibodies bound to an antigen. When combined with next-generation sequencing of immune repertoires, we were able to specifically identify clonal family members, synthesize the monoclonal antibodies, and confirm that they interact with the antigen in a manner equivalent to the corresponding polyclonal antibodies. This structure-based approach for identification of monoclonal antibodies from polyclonal sera opens new avenues for analysis of immune responses and iterative vaccine design.
PubMed: 35044813
DOI: 10.1126/sciadv.abk2039
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (3.3 Å)
構造検証レポート
Validation report summary of 7mdu
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2026-02-04に公開中

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