Miner Jacob C, Fenimore Paul W, Fischer William M, McMahon Benjamin H, Sanbonmatsu Karissa Y, Tung Chang-Shung
Theoretical Biology & Biophysics Group, Theoretical Division, Los Alamos National Laboratory, Los Alamos, NM, 87545, USA.
New Mexico Consortium, Los Alamos, NM, 87544, USA.
Curr Res Struct Biol. 2022;4:220-230. doi: 10.1016/j.crstbi.2022.06.004. Epub 2022 Jun 23.
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.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)是引发新型冠状病毒肺炎疫情并造成全球性灾难性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血管紧张素转换酶2(ACE2)的结合是导致宿主膜与病毒膜融合的第一步。尽管已经生成了大量关于SARS-CoV-2刺突蛋白的结构数据,但融合途径不同阶段的许多刺突蛋白详细结构仍不清楚,留下了大量潜在药物靶点空间未被探索。完整S2片段的原子尺度结构以及完整的融合中间体同样未知,这是我们对SARS-CoV-2感染途径认识中的主要空白。在此过程中刺突蛋白的构象变化同样也未得到很好的理解。在这里,我们展示了融合过程不同阶段的刺突蛋白结构。由于这些转变是受体结合前的必要步骤,我们提出沿转变途径的位点作为药物开发的潜在靶点。