SARS-COV-2 AND BETACORONAVIRUS: WHAT HAVE WE LEARNED IN 8 MONTHS?

被引:0
|
作者
Kwiatek, Agnieszka [1 ]
Adamczyk-Poplawska, Monika [1 ]
机构
[1] Univ Warsaw, Fac Biol, Inst Microbiol, Dept Mol Virol, Warsaw, Poland
关键词
SARS-CoV-2; betacoronavirus proteins; spike protein; furin-cleavage site; pathogenesis; ACUTE RESPIRATORY SYNDROME; CORONAVIRUS-LIKE PARTICLES; SPIKE PROTEIN; FUSION PROTEIN; VIRUS; ENTRY; REPLICATION; RECOGNITION; EXPRESSION; INTERACTS;
D O I
10.21307/PM-2020.59.3.14
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In 2019, a new human pandemic coronavirus (SARS-CoV-2) emerged in Wuhan, China. We present the knowledge about SARS-CoV-2 compared to SARS-CoV and MERS-CoV. The SARS-CoV-2 is similar to other coronaviruses, nevertheless, differences were observed. Cell entry of SARS-CoV-2 is facilitated by cleavage of spike protein by furin. The receptor-binding motif of SARS-CoV-2 spike protein forms a larger binding interface and more contacts with host receptor ACE2 compared those of in SARS-CoV. Unlike other coronaviruses, the SARS-CoV-2 spike protein has a motif; known to bind integrins. Nucleocapsid protein and RNA-dependent RNA polymerase of SA RS-CoV-2 display some structural differences compared to those of SARS-CoV as well. These features may increase the efficiency of the spread of SARS-CoV-2 and indicate the putative targets for specific antiviral therapy.
引用
收藏
页码:197 / 206
页数:10
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