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7T12

Hexameric HIV-1 (O-group) CA

7T12 の概要
エントリーDOI10.2210/pdb7t12/pdb
分子名称Capsid protein p24 (1 entity in total)
機能のキーワードcapsid, viral protein
由来する生物種HIV-1 O_MVP5180
タンパク質・核酸の鎖数12
化学式量合計305655.84
構造登録者
Jacques, D.A.,James, L.C. (登録日: 2021-12-01, 公開日: 2022-10-19, 最終更新日: 2023-10-18)
主引用文献Zuliani-Alvarez, L.,Govasli, M.L.,Rasaiyaah, J.,Monit, C.,Perry, S.O.,Sumner, R.P.,McAlpine-Scott, S.,Dickson, C.,Rifat Faysal, K.M.,Hilditch, L.,Miles, R.J.,Bibollet-Ruche, F.,Hahn, B.H.,Boecking, T.,Pinotsis, N.,James, L.C.,Jacques, D.A.,Towers, G.J.
Evasion of cGAS and TRIM5 defines pandemic HIV.
Nat Microbiol, 7:1762-1776, 2022
Cited by
PubMed Abstract: Of the 13 known independent zoonoses of simian immunodeficiency viruses to humans, only one, leading to human immunodeficiency virus (HIV) type 1(M) has become pandemic, causing over 80 million human infections. To understand the specific features associated with pandemic human-to-human HIV spread, we compared replication of HIV-1(M) with non-pandemic HIV-(O) and HIV-2 strains in myeloid cell models. We found that non-pandemic HIV lineages replicate less well than HIV-1(M) owing to activation of cGAS and TRIM5-mediated antiviral responses. We applied phylogenetic and X-ray crystallography structural analyses to identify differences between pandemic and non-pandemic HIV capsids. We found that genetic reversal of two specific amino acid adaptations in HIV-1(M) enables activation of TRIM5, cGAS and innate immune responses. We propose a model in which the parental lineage of pandemic HIV-1(M) evolved a capsid that prevents cGAS and TRIM5 triggering, thereby allowing silent replication in myeloid cells. We hypothesize that this capsid adaptation promotes human-to-human spread through avoidance of innate immune response activation.
PubMed: 36289397
DOI: 10.1038/s41564-022-01247-0
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3 Å)
構造検証レポート
Validation report summary of 7t12
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2024-11-06に公開中

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