Loading
PDBj
メニューPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

2MK3

Solution NMR structure of gp41 ectodomain monomer on a DPC micelle

2MK3 の概要
エントリーDOI10.2210/pdb2mk3/pdb
NMR情報BMRB: 19750
分子名称Transmembrane glycoprotein, chimeric construct (1 entity in total)
機能のキーワードhiv-1 env, membrane fusion, gp41 ectodomain, pre-hairpin, cores, immune system
由来する生物種Human immunodeficiency virus 1
タンパク質・核酸の鎖数1
化学式量合計8293.23
構造登録者
Roche, J.,Louis, J.M.,Grishaev, A.,Ying, J.,Bax, A. (登録日: 2014-01-23, 公開日: 2014-02-19, 最終更新日: 2024-05-01)
主引用文献Roche, J.,Louis, J.M.,Grishaev, A.,Ying, J.,Bax, A.
Dissociation of the trimeric gp41 ectodomain at the lipid-water interface suggests an active role in HIV-1 Env-mediated membrane fusion.
Proc.Natl.Acad.Sci.USA, 111:3425-3430, 2014
Cited by
PubMed Abstract: The envelope glycoprotein gp41 mediates the process of membrane fusion that enables entry of the HIV-1 virus into the host cell. The actual fusion process involves a switch from a homotrimeric prehairpin intermediate conformation, consisting of parallel coiled-coil helices, to a postfusion state where the ectodomains are arranged as a trimer of helical hairpins, adopting a six-helix bundle (6HB) state. Here, we show by solution NMR spectroscopy that a water-soluble 6HB gp41 ectodomain binds to zwitterionic detergents that contain phosphocholine or phosphatidylcholine head groups and phospholipid vesicles that mimic T-cell membrane composition. Binding results in the dissociation of the 6HB and the formation of a monomeric state, where its two α-helices, N-terminal heptad repeat (NHR) and C-terminal heptad repeat (CHR), become embedded in the lipid-water interface of the virus and host cell. The atomic structure of the gp41 ectodomain monomer, based on NOE distance restraints and residual dipolar couplings, shows that the NHR and CHR helices remain mostly intact, but they completely lose interhelical contacts. The high affinity of the ectodomain helices for phospholipid surfaces suggests that unzippering of the prehairpin intermediate leads to a state where the NHR and CHR helices become embedded in the host cell and viral membranes, respectively, thereby providing a physical force for bringing these membranes into close juxtaposition before actual fusion.
PubMed: 24550514
DOI: 10.1073/pnas.1401397111
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 2mk3
検証レポート(詳細版)ダウンロードをダウンロード

251801

件を2026-04-08に公開中

PDB statisticsPDBj update infoContact PDBjnumon