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对严重急性呼吸综合征冠状病毒S蛋白驱动感染的易感性与血管紧张素转换酶2的表达相关,并且感染可被可溶性受体阻断。

Susceptibility to SARS coronavirus S protein-driven infection correlates with expression of angiotensin converting enzyme 2 and infection can be blocked by soluble receptor.

作者信息

Hofmann Heike, Geier Martina, Marzi Andrea, Krumbiegel Mandy, Peipp Matthias, Fey Georg H, Gramberg Thomas, Pöhlmann Stefan

机构信息

Chair of Genetics, University of Erlangen-Nürnberg, 91054 Erlangen, Germany.

出版信息

Biochem Biophys Res Commun. 2004 Jul 9;319(4):1216-21. doi: 10.1016/j.bbrc.2004.05.114.

Abstract

The angiotensin converting enzyme 2 (ACE2) has been identified as a receptor for the severe acute respiratory syndrome associated coronavirus (SARS-CoV). Here we show that ACE2 expression on cell lines correlates with susceptibility to SARS-CoV S-driven infection, suggesting that ACE2 is a major receptor for SARS-CoV. The soluble ectodomain of ACE2 specifically abrogated S-mediated infection and might therefore be exploited for the generation of inhibitors. Deletion of a major portion of the cytoplasmic domain of ACE2 had no effect on S-driven infection, indicating that this domain is not important for receptor function. Our results point to a central role of ACE2 in SARS-CoV infection and suggest a minor contribution of the cytoplasmic domain to receptor function.

摘要

血管紧张素转换酶2(ACE2)已被确定为严重急性呼吸综合征相关冠状病毒(SARS-CoV)的受体。在此我们表明,细胞系上ACE2的表达与对SARS-CoV S介导感染的易感性相关,这表明ACE2是SARS-CoV的主要受体。ACE2的可溶性胞外域特异性消除了S介导的感染,因此可用于开发抑制剂。删除ACE2胞质域的大部分对S介导的感染没有影响,表明该结构域对受体功能并不重要。我们的结果表明ACE2在SARS-CoV感染中起核心作用,并提示胞质域对受体功能的贡献较小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b23c/7111153/f160b94cc251/gr1.jpg

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