Wang Hong-Wei, Wang Jia-Wei
Beijing Advanced Innovation Center for Structural Biology, Ministry of Education Key Laboratory of Protein Sciences School of Life Sciences, Tsinghua University, Beijing, 100084.
Tsinghua-Peking Joint Center for Life Sciences, Tsinghua University, Beijing, 100084.
Protein Sci. 2017 Jan;26(1):32-39. doi: 10.1002/pro.3022. Epub 2016 Sep 7.
With the ability to resolve structures of macromolecules at atomic resolution, X-ray crystallography has been the most powerful tool in modern structural biology. At the same time, recent technical improvements have triggered a resolution revolution in the single particle cryo-EM method. While the two methods are different in many respects, from sample preparation to structure determination, they both have the power to solve macromolecular structures at atomic resolution. It is important to understand the unique advantages and caveats of the two methods in solving structures and to appreciate the complementary nature of the two methods in structural biology. In this review we provide some examples, and discuss how X-ray crystallography and cryo-EM can be combined in deciphering structures of macromolecules for our full understanding of their biological mechanisms.
凭借在原子分辨率下解析大分子结构的能力,X射线晶体学一直是现代结构生物学中最强大的工具。与此同时,最近的技术改进引发了单颗粒冷冻电镜方法的分辨率革命。虽然这两种方法在从样品制备到结构测定的许多方面都有所不同,但它们都有能力在原子分辨率下解析大分子结构。了解这两种方法在解析结构方面的独特优势和注意事项,并认识到它们在结构生物学中的互补性质非常重要。在这篇综述中,我们提供了一些例子,并讨论了X射线晶体学和冷冻电镜如何结合起来解析大分子结构,以便我们全面了解其生物学机制。