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RNA结构中的工程化晶体堆积I:晶体中RNA堆积工程的过去与未来策略

Engineering Crystal Packing in RNA Structures I: Past and Future Strategies for Engineering RNA Packing in Crystals.

作者信息

Pujari Narsimha, Saundh Stephanie L, Acquah Francis A, Mooers Blaine H M, Ferré-D'Amaré Adrian R, Leung Adelaine Kwun-Wai

机构信息

Department of Veterinary Biomedical Sciences, University of Saskatchewan, Saskatoon, SK S7N 5B4, Canada.

Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.

出版信息

Crystals (Basel). 2021 Aug;11(8). doi: 10.3390/cryst11080952. Epub 2021 Aug 15.

Abstract

X-ray crystallography remains a powerful method to gain atomistic insights into the catalytic and regulatory functions of RNA molecules. However, the technique requires the preparation of diffraction-quality crystals. This is often a resource- and time-consuming venture because RNA crystallization is hindered by the conformational heterogeneity of RNA, as well as the limited opportunities for stereospecific intermolecular interactions between RNA molecules. The limited success at crystallization explains in part the smaller number of RNA-only structures in the Protein Data Bank. Several approaches have been developed to aid the formation of well-ordered RNA crystals. The majority of these are construct-engineering techniques that aim to introduce crystal contacts to favor the formation of well-diffracting crystals. A typical example is the insertion of tetraloop-tetraloop receptor pairs into non-essential RNA segments to promote intermolecular association. Other methods of promoting crystallization involve chaperones and crystallization-friendly molecules that increase RNA stability and improve crystal packing. In this review, we discuss the various techniques that have been successfully used to facilitate crystal packing of RNA molecules, recent advances in construct engineering, and directions for future research in this vital aspect of RNA crystallography.

摘要

X射线晶体学仍然是一种强大的方法,可用于从原子层面深入了解RNA分子的催化和调节功能。然而,该技术需要制备出具有衍射质量的晶体。这通常是一项耗费资源和时间的工作,因为RNA的结晶受到其构象异质性的阻碍,以及RNA分子之间立体特异性分子间相互作用的机会有限。结晶方面的有限成功部分解释了蛋白质数据库中仅含RNA结构的数量较少的原因。已经开发了几种方法来帮助形成有序的RNA晶体。其中大多数是构建体工程技术,旨在引入晶体接触以利于形成衍射良好的晶体。一个典型的例子是将四环-四环受体对插入非必需的RNA片段中以促进分子间缔合。其他促进结晶的方法涉及伴侣蛋白和有利于结晶的分子,它们可提高RNA的稳定性并改善晶体堆积。在本综述中,我们讨论了已成功用于促进RNA分子晶体堆积的各种技术、构建体工程的最新进展以及RNA晶体学这一重要方面未来的研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c91/8570644/840d30b83aa9/nihms-1734543-f0001.jpg

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