SARS-CoV-2刺突蛋白突变引起的结构和功能变化的综合分析

COVID Pub Date : 2023-09-16 DOI:10.3390/covid3090100
Aganze Gloire-Aimé Mushebenge, Samuel Chima Ugbaja, Nonkululeko Avril Mbatha, Rene B. Khan, Hezekiel M. Kumalo
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引用次数: 1

摘要

导致COVID-19大流行的SARS-CoV-2病毒的出现引发了对其刺突蛋白的激烈研究,该蛋白对病毒进入宿主细胞至关重要。病毒的繁殖和传播、宿主免疫反应调节、受体识别和宿主细胞进入机制以及结构和功能影响都与刺突蛋白的突变有关。刺突蛋白突变还可能导致免疫逃避机制,从而损害疫苗的有效性和逃逸,并且它们与疾病严重程度和临床后果有关。已经进行了大量的研究来确定这些突变对刺突蛋白结构的影响以及它如何与宿主因子相互作用。这些结果对基于刺突蛋白的药物和疫苗的设计和开发以及评估这些产品对抗新发现的刺突蛋白突变的效率具有重要意义。本文概述了刺突蛋白突变是如何分类和命名的。它进一步研究了刺突蛋白突变与临床结果、疾病严重程度、未解决的问题和未来研究前景之间的联系。此外,还探讨了这些突变对疫苗有效性的影响以及刺突蛋白突变的可能治疗靶向性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Comprehensive Analysis of Structural and Functional Changes Induced by SARS-CoV-2 Spike Protein Mutations
The emergence of SARS-CoV-2, the virus responsible for the COVID-19 pandemic, has sparked intense research on its spike protein, which is essential for viral entrance into host cells. Viral reproduction and transmission, host immune response regulation, receptor recognition and host cell entrance mechanisms, as well as structural and functional effects have all been linked to mutations in the spike protein. Spike protein mutations can also result in immune evasion mechanisms that impair vaccine effectiveness and escape, and they are linked to illness severity and clinical consequences. Numerous studies have been conducted to determine the effects of these mutations on the spike protein structure and how it interacts with host factors. These results have important implications for the design and development of medicines and vaccines based on spike proteins as well as for the assessment of those products’ efficiency against newly discovered spike protein mutations. This paper gives a general overview of how spike protein mutations are categorized and named. It further looks at the links between spike protein mutations and clinical outcomes, illness severity, unanswered problems, and future research prospects. Additionally, explored are the effects of these mutations on vaccine effectiveness as well as the possible therapeutic targeting of spike protein mutations.
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