利用计算方法识别冠状病毒刺突蛋白的重要基序

Manjusha Nair, A. R, Arya C. Babu
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摘要

迄今为止,冠状病毒(SARS-CoV-2)的不同突变变体影响了世界上很大一部分人口。从这个角度来看,任何了解病毒对疫苗和药物免疫的研究都具有更大的意义。血管紧张素转换酶2 (Angiotensin-converting enzyme, ACE2)是SARS-COV-2 S蛋白的主要进入受体,研究ACE2对了解宿主细胞中的SARS-COV-2感染具有重要意义。在刺突糖蛋白中发现的各种基序的功能意义及其构象变化已经被研究,以更好地了解其发病机制。本文所描述的计算研究集中于病毒的疾病传播机制,特别是病毒感染期间的受体识别机制。本研究使用不同的计算技术来鉴定sars - cov - 2s糖蛋白的重要基序。将不同的冠状病毒基因组与参考基因组(武汉海鲜市场分离物)进行了比较,并根据病毒感染关键基序的相似性提出了病毒可能的中间宿主。本文利用计算技术重新回顾了先前对蛋白水解裂解位点S蛋白基序的研究,以提示可能的感染中间宿主。
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Recognizing Significant Motifs of Corona Virus Spike Proteins using Computational Approaches
The different mutated variants of Corona Virus (SARS-CoV-2), affected a large percentage of the world population so far. On this light, any study on understanding the virus’s immunity to vaccines and medicines has greater relevance. Studies on Angiotensin-converting enzyme 2 (ACE2), the main entry receptor for the SARS-COV-2 S protein is significantly important in understanding SARS-COV-2 infection in host cells. The functional implications of various motifs found in the spike glycoprotein and its conformational changes had been studied previously to better understand the pathogenesis. The computational study, described herein, have focused on the disease transmission mechanisms of the virus especially on the receptor recognition mechanisms during viral infection. This study used different computational techniques to identify significant motif of the SARS-CoV-2 S Glycoprotein. Different corona viral genomes were compared against the reference genome (Wuhan seafood market isolate) and the possible intermediate hosts of the virus has been proposed based on the similarity in the motifs which are critical for viral infections. Previous studies on S protein motifs of proteolytic cleavage site are revisited here using computational techniques to suggest the possible intermediate hosts of infection.
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