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通过 NMR 光谱筛选蛋白质-单链 RNA 复合物以确定结构。

Screening protein--single stranded RNA complexes by NMR spectroscopy for structure determination.

机构信息

Department of Biochemistry, Henry Wellcome Laboratories of Structural Biology, University of Leicester, UK.

Department of Biochemistry, Henry Wellcome Laboratories of Structural Biology, University of Leicester, UK.

出版信息

Methods. 2014 Feb;65(3):288-301. doi: 10.1016/j.ymeth.2013.09.018. Epub 2013 Oct 1.

Abstract

In the past few years, RNA molecules have been revealed to be at the center of numerous biological processes. Long considered as passive molecules transferring genetic information from DNA to proteins, it is now well established that RNA molecules play important regulatory roles. Associated with that, the number of identified RNA binding proteins (RBPs) has increased considerably and mutations in RNA molecules or RBP have been shown to cause various diseases, such as cancers. It is therefore crucial to understand at the molecular level how these proteins specifically recognise their RNA targets in order to design new generation drug therapies targeting protein-RNA complexes. Nuclear magnetic resonance (NMR) is a particularly well-suited technique to study such protein-RNA complexes at the atomic level and can provide valuable information for new drug discovery programs. In this article, we describe the NMR strategy that we and other laboratories use for screening optimal conditions necessary for structural studies of protein-single stranded RNA complexes, using two proteins, Sam68 and T-STAR, as examples.

摘要

在过去的几年中,RNA 分子已被揭示处于许多生物过程的中心。长期以来,人们一直认为 RNA 分子是将遗传信息从 DNA 传递到蛋白质的被动分子,但现在已经明确,RNA 分子发挥着重要的调节作用。与此相关,已鉴定出的 RNA 结合蛋白 (RBP) 的数量大大增加,并且已经表明 RNA 分子或 RBP 的突变会导致各种疾病,如癌症。因此,了解这些蛋白质如何在分子水平上特异性识别其 RNA 靶标至关重要,以便设计针对蛋白-RNA 复合物的新一代药物疗法。核磁共振 (NMR) 是一种特别适合在原子水平上研究此类蛋白-RNA 复合物的技术,可为新药发现计划提供有价值的信息。在本文中,我们描述了我们和其他实验室使用的 NMR 策略,该策略用于筛选用于研究蛋白-单链 RNA 复合物结构的最佳条件,Sam68 和 T-STAR 这两种蛋白就是例子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2f7/3969250/883c777dd94d/gr1.jpg

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