Structural biology of SARS-CoV-2 accessory proteins

被引:0
|
作者
Briggs, David C. [1 ]
Kandler, Luise [2 ]
Schmidt, Lisa [2 ]
Santoni, Gianluca [3 ]
Thorn, Andrea [2 ]
机构
[1] Francis Crick Inst, Signalling & Struct Biol Lab, London, England
[2] Univ Hamburg, Inst Nanostruct & Solid State Phys, Luruper Chaussee, Hamburg, Germany
[3] European Synchrotron Radiat Facil, Grenoble, France
基金
英国医学研究理事会; 英国惠康基金;
关键词
SARS-CoV-2; COVID-19; accessory proteins; interferon; corona; ORF3A;
D O I
10.1080/0889311X.2023.2173744
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
The coronavirus SARS-CoV-2 is the causative agent for the COVID-19 pandemic. Its proteome is typically separated into three classes of proteins: (1) Structural proteins which facilitate the transport and host cell infiltration of the viral RNA, (2) non-structural proteins which are thought to be essential for the viral life cycle and are all produced from open reading frame 1ab (ORF1ab) on the RNA, and (3) everything else, called accessory proteins. Although it was originally thought that these accessory proteins are non-essential for viral replication, a growing body of evidence suggests that these diverse proteins have crucial roles in virus-host interactions, in particular in the way they interfere with the signalling pathways that modulate the host cell's response to infection and viral pathogenicity. Here, we summarize efforts to structurally characterize the accessory proteins from SARS-CoV-2.
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页码:3 / 18
页数:16
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