Bodakuntla Satish, Kuhn Christopher Cyrus, Biertümpfel Christian, Mizuno Naoko
Laboratory of Structural Cell Biology, National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, MD, United States.
National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, United States.
Front Mol Biosci. 2023 Oct 6;10:1252529. doi: 10.3389/fmolb.2023.1252529. eCollection 2023.
Cryogenic electron microscopy (cryo-EM) and electron tomography (cryo-ET) have become a critical tool for studying viral particles. Cryo-EM has enhanced our understanding of viral assembly and replication processes at a molecular resolution. Meanwhile, cryo-ET has been used to investigate how viruses attach to and invade host cells. These advances have significantly contributed to our knowledge of viral biology. Particularly, prompt elucidations of structures of the SARS-CoV-2 spike protein and its variants have directly impacted the development of vaccines and therapeutic measures. This review discusses the progress made by cryo-EM based technologies in comprehending the severe acute respiratory syndrome coronavirus-2 (SARS-Cov-2), the virus responsible for the devastating global COVID-19 pandemic in 2020 with focus on the SARS-CoV-2 spike protein and the mechanisms of the virus entry and replication.
低温电子显微镜(cryo-EM)和电子断层扫描(cryo-ET)已成为研究病毒颗粒的关键工具。低温电子显微镜在分子分辨率上增强了我们对病毒组装和复制过程的理解。同时,低温电子断层扫描已被用于研究病毒如何附着并侵入宿主细胞。这些进展极大地促进了我们对病毒生物学的认识。特别是,对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白及其变体结构的迅速阐明直接影响了疫苗和治疗措施的开发。本综述讨论了基于低温电子显微镜的技术在理解严重急性呼吸综合征冠状病毒2(SARS-CoV-2)方面取得的进展,该病毒是2020年造成全球毁灭性COVID-19大流行的元凶,重点关注SARS-CoV-2刺突蛋白以及病毒进入和复制的机制。