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Nat Methods ; 20(1): 65-69, 2023 01.
Article in English | MEDLINE | ID: mdl-36550273

ABSTRACT

Ultraviolet crosslinking and immunoprecipitation (CLIP) methodologies enable the identification of RNA binding sites of RNA-binding proteins (RBPs). Despite improvements in the library preparation of RNA fragments, the enhanced CLIP (eCLIP) protocol requires 4 days of hands-on time and lacks the ability to process several RBPs in parallel. We present a new method termed antibody-barcode eCLIP that utilizes DNA-barcoded antibodies and proximity ligation of the DNA oligonucleotides to RBP-protected RNA fragments to interrogate several RBPs simultaneously. We observe performance comparable with that of eCLIP with the advantage of dramatically increased scaling while maintaining the same material requirement of a single eCLIP experiment.


Subject(s)
RNA , Transcriptome , RNA/genetics , Binding Sites , Protein Binding , RNA-Binding Proteins/metabolism , Antibodies/chemistry , Immunoprecipitation
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