未能成功:在RNA - RNA复合物的结构研究中防止RNA切割的技术

IF 3.5 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Seth P. Jones , Christian Goossen , Sean D. Lewis , Annie M. Delaney , Michael L. Gleghorn
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引用次数: 0

摘要

核糖核酸酶在其切割靶向的RNA结构和序列上各不相同,是细胞中的一种重要类型的酶。尽管已知RNase和具有确定三维结构的RNase的实例很多,但在切割前RNase与完整同源RNA底物结合的实例相对较少。为了更好地理解RNA酶的结构和RNA靶标的序列特异性,已经为许多不同的RNA酶开发了用于组装这些以预切割状态捕获的酶复合物的体外方法。我们调查了蛋白质数据库中的此类结构,并在本综述中详细介绍了成功使用的方法,并将其与相应的结构联系起来。我们还为未来的方法开发提供了想法和建议。这篇综述中的许多策略可以与X射线晶体学、冷冻电镜和其他结构求解技术结合使用。我们希望这篇综述将作为解决未来尚未确定的RNase底物复杂结构的指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Not making the cut: Techniques to prevent RNA cleavage in structural studies of RNase–RNA complexes

Not making the cut: Techniques to prevent RNA cleavage in structural studies of RNase–RNA complexes

RNases are varied in the RNA structures and sequences they target for cleavage and are an important type of enzyme in cells. Despite the numerous examples of RNases known, and of those with determined three-dimensional structures, relatively few examples exist with the RNase bound to intact cognate RNA substrate prior to cleavage. To better understand RNase structure and sequence specificity for RNA targets, in vitro methods used to assemble these enzyme complexes trapped in a pre-cleaved state have been developed for a number of different RNases. We have surveyed the Protein Data Bank for such structures and in this review detail methodologies that have successfully been used and relate them to the corresponding structures. We also offer ideas and suggestions for future method development. Many strategies within this review can be used in combination with X-ray crystallography, as well as cryo-EM, and other structure-solving techniques. Our hope is that this review will be used as a guide to resolve future yet-to-be-determined RNase–substrate complex structures.

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来源期刊
Journal of Structural Biology: X
Journal of Structural Biology: X Biochemistry, Genetics and Molecular Biology-Structural Biology
CiteScore
6.50
自引率
0.00%
发文量
20
审稿时长
62 days
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