De Zorzi Rita, Mi Wei, Liao Maofu, Walz Thomas
Department of Cell Biology, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA Howard Hughes Medical Institute, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA.
Department of Cell Biology, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA.
Microscopy (Oxf). 2016 Feb;65(1):81-96. doi: 10.1093/jmicro/dfv058. Epub 2015 Oct 15.
Single-particle electron microscopy (EM) provides the great advantage that protein structure can be studied without the need to grow crystals. However, due to technical limitations, this approach played only a minor role in the study of membrane protein structure. This situation has recently changed dramatically with the introduction of direct electron detection device cameras, which allow images of unprecedented quality to be recorded, also making software algorithms, such as three-dimensional classification and structure refinement, much more powerful. The enhanced potential of single-particle EM was impressively demonstrated by delivering the first long-sought atomic model of a member of the biomedically important transient receptor potential channel family. Structures of several more membrane proteins followed in short order. This review recounts the history of single-particle EM in the study of membrane proteins, describes the technical advances that now allow this approach to generate atomic models of membrane proteins and provides a brief overview of some of the membrane protein structures that have been studied by single-particle EM to date.
单颗粒电子显微镜(EM)具有很大的优势,即无需生长晶体就能研究蛋白质结构。然而,由于技术限制,这种方法在膜蛋白结构研究中仅发挥了次要作用。随着直接电子检测设备相机的引入,这种情况最近发生了巨大变化,该相机能够记录前所未有的高质量图像,也使得诸如三维分类和结构精修等软件算法更加强大。通过提供生物医学上重要的瞬时受体电位通道家族成员的首个长期以来一直寻求的原子模型,单颗粒EM的增强潜力得到了令人印象深刻的展示。随后很快又有几种更多膜蛋白的结构被解析出来。这篇综述讲述了单颗粒EM在膜蛋白研究中的历史,描述了目前使这种方法能够生成膜蛋白原子模型的技术进步,并简要概述了迄今为止通过单颗粒EM研究的一些膜蛋白结构。