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血管紧张素转换酶2:严重急性呼吸综合征冠状病毒的功能性受体。

Angiotensin-converting enzyme 2: a functional receptor for SARS coronavirus.

作者信息

Kuhn J H, Li W, Choe H, Farzan M

机构信息

Partners AIDS Research Center, Brigham and Women's Hospital, Department of Medicine (Microbiology and Molecular Genetics), Harvard Medical School, Cambridge, Massachusetts 02139, USA.

出版信息

Cell Mol Life Sci. 2004 Nov;61(21):2738-43. doi: 10.1007/s00018-004-4242-5.

Abstract

Cellular entry of enveloped viruses is often dependent on attachment proteins expressed on the host cell surface. Viral envelope proteins bind these receptors, and, in an incompletely understood process, facilitate fusion of the cellular and viral membranes so as to introduce the viral core into the cytoplasm. Only a small fraction of viral receptors have been identified so far. Recently, a novel coronavirus was identified as the etiological agent of severe acute respiratory syndrome (SARS). The fusion protein gene of SARS coronavirus (SARS-CoV) was cloned and characterized, and shortly thereafter, angiotensin-converting enzyme 2 (ACE2) was shown to be its functional receptor. Identification of ACE2 as a receptor for SARS-CoV will likely contribute to the development of antivirals and vaccines. It may also contribute to the development of additional animal models for studying SARS pathogenesis, and could help identify the animal reservoir of SARS-CoV.

摘要

包膜病毒的细胞进入通常依赖于宿主细胞表面表达的附着蛋白。病毒包膜蛋白与这些受体结合,并且在一个尚未完全理解的过程中,促进细胞膜与病毒膜的融合,从而将病毒核心引入细胞质。到目前为止,仅鉴定出一小部分病毒受体。最近,一种新型冠状病毒被确定为严重急性呼吸综合征(SARS)的病原体。克隆并鉴定了SARS冠状病毒(SARS-CoV)的融合蛋白基因,此后不久,血管紧张素转换酶2(ACE2)被证明是其功能性受体。将ACE2鉴定为SARS-CoV的受体可能有助于抗病毒药物和疫苗的开发。它也可能有助于开发用于研究SARS发病机制的其他动物模型,并有助于确定SARS-CoV的动物宿主。

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