| Literature DB >> 35171487 |
Michael Backlund1,2,3,4, Andreas E Kulozik5,6,7,8.
Abstract
RNA-binding proteins are key mediators of many of the RNA-regulatory functions throughout the RNA life cycle in the nucleus and in the cytoplasm. The invention and the recent refinement of the RNA-interactome capture technology has now enabled the analysis of the global RNA-interactome in living cells in the nucleus and in the cytoplasm separately. This technology thus allows an unprecedented differential view on the function of RNA-binding proteins in these compartments. Here we describe a method combining nucleo-cytoplasmic fractionation and enhanced RNA-interactome capture (eRIC) for studying RBPs binding to polyadenylated RNAs separately in the cytoplasmic and in the nuclear compartments.Entities:
Keywords: Locked nucleic acid; Nucleo-cytoplasmic fractionation; RNA; RNA Interactome capture; RNA-binding protein
Mesh:
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Year: 2022 PMID: 35171487 DOI: 10.1007/978-1-0716-1975-9_18
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745