Abstract
The majority of the mammalian genome is transcribed into non-coding RNAs, many of which co-evolve with RNA-binding proteins (RBPs) to function as biochemically defined and tractable ribonucleoproteins (RNPs). Here, we applied icSHAPE- a robust and versatile RNA structural probing pipeline- to endogenous RNPs purified from nuclei, providing base-resolution structural rationale for RNP activity and subcellular localization. Combining with genetic and biochemical reconstitutions, structural and functional alternations can be directly attributed to a given RBP without ambiguity. For complete details on the use and execution of this protocol, please refer to Chen et al. (2018).
Original language | English |
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Pages (from-to) | 100477 |
Number of pages | 1 |
Journal | STAR Protocols |
Volume | 2 |
Issue number | 2 |
DOIs | |
State | Published - Jun 18 2021 |
Keywords
- CRISPR
- Cell separation/fractionation
- Gene Expression
- Molecular Biology
- Protein expression and purification
- RNA-seq
- Sequencing
- Structural Biology