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RNA 全组织原位杂交邻近连接分析(rISH-PLA),一种用于检测完整细胞中 RNA-蛋白质复合物的分析方法。

RNA Whole-Mount In Situ Hybridization Proximity Ligation Assay (rISH-PLA), an Assay for Detecting RNA-Protein Complexes in Intact Cells.

作者信息

Roussis Ioannis M, Myers Fiona A, Scarlett Garry P

机构信息

Biophysics Laboratories, Institute of Biomedical and Biomolecular Sciences, University of Portsmouth, Portsmouth, United Kingdom.

出版信息

Curr Protoc Cell Biol. 2017 Mar 3;74:17.20.1-17.20.10. doi: 10.1002/cpcb.13.

Abstract

Techniques for studying RNA-protein interactions have lagged behind those for DNA-protein interactions as a consequence of the complexities associated with working with RNA. This unit describes a method for the adaptation of the In Situ Hybridization-Proximity Ligation Assay (ISH-PLA) to the study of RNA regulation (rISH-PLA). The rISH-PLA assay allows the identification of a given RNA-protein complex at subcellular and single-cell resolution, thus avoiding the lack of spatial resolution and sensitivity associated with assaying heterogeneous cell populations from which conventional RNA-protein interaction detection techniques suffer. This technique will be particularly usefully for studying the activity of RNA binding proteins (RBPs) in complex mixtures of cells, for example tissue sections or whole embryos. © 2017 by John Wiley & Sons, Inc.

摘要

由于处理RNA存在复杂性,用于研究RNA - 蛋白质相互作用的技术落后于用于研究DNA - 蛋白质相互作用的技术。本单元描述了一种将原位杂交 - 邻近连接分析(ISH - PLA)应用于RNA调控研究(rISH - PLA)的方法。rISH - PLA分析能够在亚细胞和单细胞分辨率下鉴定特定的RNA - 蛋白质复合物,从而避免了传统RNA - 蛋白质相互作用检测技术在分析异质细胞群体时所面临的空间分辨率和灵敏度不足的问题。该技术对于研究细胞复杂混合物(如组织切片或整个胚胎)中RNA结合蛋白(RBP)的活性将特别有用。© 2017约翰威立国际出版公司

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