SARS-CoV-2刺突蛋白在融合过程中的整合结构研究(2022)

IF 2.7 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jacob C. Miner , Paul W. Fenimore , William M. Fischer , Benjamin H. McMahon , Karissa Y. Sanbonmatsu , Chang-Shung Tung
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引用次数: 0

摘要

SARS-CoV-2是导致COVID-19大流行和灾难性的全球健康和经济影响的病毒。病毒表面的刺突蛋白负责病毒进入宿主细胞。刺突蛋白与宿主细胞受体ACE2的结合是导致宿主和病毒膜融合的第一步。尽管对SARS-CoV-2的刺突蛋白已经产生了大量的结构数据,但在融合途径的不同阶段,刺突蛋白的许多详细结构是未知的,留下了丰富的潜在药物靶点空间未被探索。完整的S2片段的原子尺度结构以及完整的融合中间体也是未知的,这是我们对sars - cov -2感染途径的认识的主要空白。在这个过程中,刺突蛋白的构象变化也同样没有得到很好的理解。在这里,我们展示了融合过程中不同阶段刺突蛋白的结构。由于过渡是受体结合之前的必要步骤,我们提出了沿过渡途径的位点作为药物开发的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Integrative structural studies of the SARS-CoV-2 spike protein during the fusion process (2022)

Integrative structural studies of the SARS-CoV-2 spike protein during the fusion process (2022)

SARS-CoV-2 is the virus responsible for the COVID-19 pandemic and catastrophic, worldwide health and economic impacts. The spike protein on the viral surface is responsible for viral entry into the host cell. The binding of spike protein to the host cell receptor ACE2 is the first step leading to fusion of the host and viral membranes. Despite the vast amount of structure data that has been generated for the spike protein of SARS-CoV-2, many of the detailed structures of the spike protein in different stages of the fusion pathway are unknown, leaving a wealth of potential drug-target space unexplored. The atomic-scale structure of the complete S2 segment, as well as the complete fusion intermediate are also unknown and represent major gaps in our knowledge of the infectious pathway of SAR-CoV-2. The conformational changes of the spike protein during this process are similarly not well understood. Here we present structures of the spike protein at different stages of the fusion process. With the transitions being a necessary step before the receptor binding, we propose sites along the transition pathways as potential targets for drug development.

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来源期刊
CiteScore
4.60
自引率
0.00%
发文量
33
审稿时长
104 days
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