Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, British Columbia, Canada, V6T 1Z3.
Gandeeva Therapeutics Inc., Vancouver, British Columbia, Canada, V5C 6N5.
Chem Rev. 2022 Sep 14;122(17):14066-14084. doi: 10.1021/acs.chemrev.1c01062. Epub 2022 Jul 21.
The global spread of SARS-CoV-2 has proceeded at an unprecedented rate. Remarkably, characterization of the virus using modern tools in structural biology has also progressed at exceptional speed. Advances in electron-based imaging techniques, combined with decades of foundational studies on related viruses, have enabled the research community to rapidly investigate structural aspects of the novel coronavirus from the level of individual viral proteins to imaging the whole virus in a native context. Here, we provide a detailed review of the structural biology and pathobiology of SARS-CoV-2 as it relates to all facets of the viral life cycle, including cell entry, replication, and three-dimensional (3D) packaging based on insights obtained from X-ray crystallography, cryo-electron tomography, and single-particle cryo-electron microscopy. The structural comparison between SARS-CoV-2 and the related earlier viruses SARS-CoV and MERS-CoV is a common thread throughout this review. We conclude by highlighting some of the outstanding unanswered structural questions and underscore areas that are under rapid current development such as the design of effective therapeutics that block viral infection.
SARS-CoV-2 在全球的传播速度前所未有。值得注意的是,利用结构生物学中的现代工具对该病毒进行的特征描述也以非凡的速度取得进展。基于电子的成像技术的进步,加上几十年来对相关病毒的基础研究,使研究界能够迅速从单个病毒蛋白的水平研究新型冠状病毒的结构方面,并在天然环境中对整个病毒进行成像。在这里,我们详细回顾了 SARS-CoV-2 的结构生物学和发病生物学,涉及病毒生命周期的各个方面,包括基于 X 射线晶体学、冷冻电子断层扫描和单颗粒冷冻电子显微镜获得的见解的细胞进入、复制和三维(3D)包装。SARS-CoV-2 与相关的早期病毒 SARS-CoV 和 MERS-CoV 之间的结构比较是本综述的一个共同主题。最后,我们强调了一些悬而未决的突出结构问题,并强调了一些正在迅速发展的领域,例如设计有效阻止病毒感染的治疗方法。