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人类冠状病毒刺突蛋白与宿主受体的识别。

Human coronavirus spike protein-host receptor recognition.

机构信息

School of Chemistry, University of Hyderabad, Hyderabad, 500046, India.

出版信息

Prog Biophys Mol Biol. 2021 May;161:39-53. doi: 10.1016/j.pbiomolbio.2020.10.006. Epub 2020 Oct 31.

Abstract

A variety of coronaviruses (CoVs) have infected humans and caused mild to severe respiratory diseases that could result in mortality. The human CoVs (HCoVs) belong to the genera of α- and β-CoVs that originate in rodents and bats and are transmitted to humans via zoonotic contacts. The binding of viral spike proteins to the host cell receptors is essential for mediating fusion of viral and host cell membranes to cause infection. The SARS-CoV-2 originated in bats (RaTG13 SARS-CoV) and is transmitted to humans via pangolins. The presence of 'PRRA' sequence motif in SARS-CoV-2 spike proteins from human, dog, cat, mink, tiger and lion suggests a common viral entry mechanism into host cells. In this review, we discuss structural features of HCoV spike proteins and recognition of host protein and carbohydrate receptors.

摘要

多种冠状病毒(CoVs)已感染人类,并导致从轻微到严重的呼吸道疾病,甚至可能导致死亡。人类冠状病毒(HCoVs)属于α和β冠状病毒属,源自啮齿动物和蝙蝠,并通过动物与人类之间的接触传播给人类。病毒刺突蛋白与宿主细胞受体的结合对于介导病毒和宿主细胞膜融合以引起感染至关重要。SARS-CoV-2 起源于蝙蝠(RaTG13 SARS-CoV),并通过穿山甲传播给人类。来自人类、狗、猫、水貂、老虎和狮子的 SARS-CoV-2 刺突蛋白中存在“PRRA”序列基序,表明存在进入宿主细胞的共同病毒进入机制。在这篇综述中,我们讨论了 HCoV 刺突蛋白的结构特征以及对宿主蛋白和碳水化合物受体的识别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc15/7604128/48efb355c8a4/gr1a_lrg.jpg

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