Isotope-free mapping of protein-RNA interactions at single-nucleotide resolution by iCLIP3
Individual-nucleotide resolution UV crosslinking and immunoprecipitation (iCLIP) enables transcriptome-wide mapping of RNA-binding protein (RBP)-RNA interactions. Here, we present iCLIP version 3 (iCLIP3), a streamlined protocol optimized for generating high-quality iCLIP libraries from low-input material. We describe steps for near-infrared visualization of RBP-RNA complexes, silica column-based RNA isolation, and unique dual indexing using TruSeq adapters for cost-effective multiplexing and sequencing. We detail a complete bioinformatics workflow to identify crosslinking events and define RBP binding sites from raw sequencing data.
Authors
- Melina Klostermann (ORCID: https://orcid.org/0000-0003-3122-1095)
- Anke Busch (ORCID: https://orcid.org/0000-0002-2232-1329)
- Michaela Müller-McNicoll (ORCID: https://orcid.org/0000-0002-7174-8310)
- Vladimir Despic
- Mikhail Mesitov
- Julian König
- Anna Orekhova
- Kathi Zarnack
Institutions
- Goethe University Frankfurt (DE)
- Acatech (DE)
- University of Würzburg (DE)
- Max Planck Institute of Biophysics (DE)
- Institute of Molecular Biology (DE)
- Frankfurt University of Applied Sciences (DE)
Publication Details
- Journal
- STAR Protocols
- Published
- 2026-07-17
- DOI
- https://doi.org/10.1016/j.xpro.2026.104704
- Primary Topic
- RNA Research and Splicing
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Deutsche Forschungsgemeinschaft