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研究剪接体解旋酶的结构与功能。

Studying structure and function of spliceosomal helicases.

作者信息

Ficner Ralf, Dickmanns Achim, Neumann Piotr

机构信息

Department of Molecular Structural Biology, Institute of Microbiology and Genetics, GZMB, Georg-August-University Göttingen, 37077 Göttingen, Germany.

Department of Molecular Structural Biology, Institute of Microbiology and Genetics, GZMB, Georg-August-University Göttingen, 37077 Göttingen, Germany.

出版信息

Methods. 2017 Aug 1;125:63-69. doi: 10.1016/j.ymeth.2017.06.028. Epub 2017 Jun 29.

Abstract

The splicing of eukaryotic precursor mRNAs requires the activity of at least three DEAD-box helicases, one Ski2-like helicase and four DEAH-box helicases. High resolution structures for five of these spliceosomal helicases were obtained by means of X-ray crystallography. Additional low resolution structural information could be derived from single particle cryo electron microscopy and small angle X-ray scattering. The functional characterization includes biochemical methods to measure the ATPase and helicase activities. This review gives an overview on the techniques used to gain insights in to the structure and function of spliceosomal helicases.

摘要

真核生物前体mRNA的剪接至少需要三种DEAD-box解旋酶、一种Ski2样解旋酶和四种DEAH-box解旋酶的活性。通过X射线晶体学获得了其中五种剪接体解旋酶的高分辨率结构。另外的低分辨率结构信息可从单颗粒冷冻电子显微镜和小角X射线散射中获得。功能表征包括测量ATP酶和解旋酶活性的生化方法。本综述概述了用于深入了解剪接体解旋酶结构和功能的技术。

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