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6VU2

M1214_N1 Fab structure

6VU2 の概要
エントリーDOI10.2210/pdb6vu2/pdb
分子名称M1214 N1 Fab heavy chain, M1214 N1 Fab light chain (3 entities in total)
機能のキーワードantibody, gp120, immune system
由来する生物種Human immunodeficiency virus
詳細
タンパク質・核酸の鎖数2
化学式量合計46553.99
構造登録者
Pan, R.,Kong, X. (登録日: 2020-02-14, 公開日: 2020-05-06, 最終更新日: 2024-10-23)
主引用文献Jia, M.,Liberatore, R.A.,Guo, Y.,Chan, K.W.,Pan, R.,Lu, H.,Waltari, E.,Mittler, E.,Chandran, K.,Finzi, A.,Kaufmann, D.E.,Seaman, M.S.,Ho, D.D.,Shapiro, L.,Sheng, Z.,Kong, X.P.,Bieniasz, P.D.,Wu, X.
VSV-Displayed HIV-1 Envelope Identifies Broadly Neutralizing Antibodies Class-Switched to IgG and IgA.
Cell Host Microbe, 27:963-, 2020
Cited by
PubMed Abstract: The HIV-1 envelope (Env) undergoes conformational changes during infection. Broadly neutralizing antibodies (bNAbs) are typically isolated by using soluble Env trimers, which do not capture all Env states. To address these limitations, we devised a vesicular stomatitis virus (VSV)-based probe to display membrane-embedded Env trimers and isolated five bNAbs from two chronically infected donors, M4008 and M1214. Donor B cell receptor (BCR) repertoires identified two bNAb lineages, M4008_N1 and M1214_N1, that class-switched to immunoglobulin G (IgG) and IgA. Variants of these bNAbs reconstituted as IgA demonstrated broadly neutralizing activity, and the IgA fraction of M1214 plasma conferred neutralization. M4008_N1 epitope mapping revealed a glycan-independent V3 epitope conferring tier 2 virus neutralization. A 4.86-Å-resolution cryogenic electron microscopy (cryo-EM) structure of M1214_N1 complexed with CH505 SOSIP revealed another elongated epitope, the V2V5 corridor, extending from V2 to V5. Overall, the VSV probe identified bNAb lineages with neutralizing IgG and IgA members targeting distinct sites of HIV-1 Env vulnerability.
PubMed: 32315598
DOI: 10.1016/j.chom.2020.03.024
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.19 Å)
構造検証レポート
Validation report summary of 6vu2
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2025-07-16に公開中

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