Cianfrocco Michael A, Kellogg Elizabeth H
Life Sciences Institute and Department of Biological Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.
Department of Molecular Biology and Genetics,Cornell University, Ithaca, New York 14850, United States.
J Chem Inf Model. 2020 May 26;60(5):2458-2469. doi: 10.1021/acs.jcim.9b01178. Epub 2020 Mar 9.
Cryo-electron microscopy (cryo-EM) has enjoyed explosive recent growth due to revolutionary advances in hardware and software, resulting in a steady stream of long-awaited, high-resolution structures with unprecedented atomic detail. With this comes an increased number of microscopes, cryo-EM facilities, and scientists eager to leverage the ability to determine protein structures without crystallization. However, numerous pitfalls and considerations beset the path toward high-resolution structures and are not necessarily obvious from literature surveys. Here, we detail the most common misconceptions when initiating a cryo-EM project and common technical hurdles, as well as their solutions, and we conclude with a vision for the future of this exciting field.
由于硬件和软件方面的革命性进展,冷冻电子显微镜(cryo-EM)近年来得到了迅猛发展,从而源源不断地产生了一大批人们期待已久的、具有前所未有的原子细节的高分辨率结构。随之而来的是显微镜数量的增加、冷冻电子显微镜设施的增多,以及渴望利用无需结晶就能确定蛋白质结构这一能力的科学家数量的增加。然而,在通往高分辨率结构的道路上存在许多陷阱和需要考虑的因素,而这些从文献调研中不一定能明显看出。在这里,我们详细阐述了启动冷冻电子显微镜项目时最常见的误解和常见的技术障碍,以及它们的解决方案,最后我们展望了这个令人兴奋的领域的未来。