Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
FEBS J. 2013 Jan;280(1):28-45. doi: 10.1111/febs.12078. Epub 2012 Dec 17.
Cryo-electron microscopy (cryo-EM) is increasingly becoming a mainstream technology for studying the architecture of cells, viruses and protein assemblies at molecular resolution. Recent developments in microscope design and imaging hardware, paired with enhanced image processing and automation capabilities, are poised to further advance the effectiveness of cryo-EM methods. These developments promise to increase the speed and extent of automation, and to improve the resolutions that may be achieved, making this technology useful to determine a wide variety of biological structures. Additionally, established modalities for structure determination, such as X-ray crystallography and nuclear magnetic resonance spectroscopy, are being routinely integrated with cryo-EM density maps to achieve atomic-resolution models of complex, dynamic molecular assemblies. In this review, which is directed towards readers who are not experts in cryo-EM methodology, we provide an overview of emerging themes in the application of this technology to investigate diverse questions in biology and medicine. We discuss the ways in which these methods are being used to study structures of macromolecular assemblies that range in size from whole cells to small proteins. Finally, we include a description of how the structural information obtained by cryo-EM is deposited and archived in a publicly accessible database.
冷冻电子显微镜(cryo-EM)技术越来越成为研究细胞、病毒和蛋白质组装体分子结构的主流技术。显微镜设计和成像硬件的最新进展,加上增强的图像处理和自动化功能,有望进一步提高 cryo-EM 方法的效率。这些发展有望提高自动化的速度和程度,并提高可能达到的分辨率,使这项技术能够用于确定各种生物结构。此外,用于结构确定的成熟模式,如 X 射线晶体学和核磁共振波谱学,正被常规地与 cryo-EM 密度图相结合,以实现复杂、动态分子组装体的原子分辨率模型。在这篇面向 cryo-EM 方法学非专家读者的综述中,我们概述了该技术在生物学和医学领域的各种问题研究中的应用中的新兴主题。我们讨论了这些方法如何用于研究从整个细胞到小蛋白质等各种大小的大分子组装体的结构。最后,我们还介绍了 cryo-EM 获得的结构信息如何以可公开访问的数据库的形式进行存储和归档。