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Beyond X-rays: an overview of emerging structural biology methods

机译:超越X射线:新兴结构生物学方法的概述

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Structural biologists rely on X-ray crystallography as the main technique for determining the three-dimensional structures of macromolecules; however, in recent years, new methods that go beyond X-ray-based technologies are broadening the selection of tools to understand molecular structure and function. Simultaneously, national facilities are developing programming tools and maintaining personnel to aid novice structural biologists in de novo structure determination. The combination of X-ray free electron lasers (XFELs) and serial femtosecond crystallography (SFX) now enable time-resolved structure determination that allows for capture of dynamic processes, such as reaction mechanism and conformational flexibility. XFEL and SFX, along with microcrystal electron diffraction (MicroED), help side-step the need for large crystals for structural studies. Moreover, advances in cryogenic electron microscopy (cryo-EM) as a tool for structure determination is revolutionizing how difficult to crystallize macromolecules and/or complexes can be visualized at the atomic scale. This review aims to provide a broad overview of these new methods and to guide readers to more in-depth literature of these methods.
机译:结构生物学家依靠X射线晶体学作为确定大分子三维结构的主要技术。但是,近年来,超出基于X射线的技术的新方法正在扩大了解分子结构和功能的工具的选择。同时,国家设施正在开发编程工具和维护人员,以帮助新手结构生物学家从头结构确定。现在,X射线游离电子激光器(XFELS)和串行飞秒晶体学(SFX)的组合可以实现时间分辨的结构测定,从而允许捕获动态过程,例如反应机理和构象灵活性。 XFEL和SFX以及微晶电子衍射(微晶体),有助于辅助大型晶体进行结构研究。此外,作为结构确定工具的低温电子显微镜(Cryo-EM)的进步正在革新如何在原子尺度上可视化多难以结晶的大分子和/或复合物。这篇评论旨在提供这些新方法的广泛概述,并指导读者了解这些方法的更深入文献。

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