Revolutionize the ability to identify RBP binding sites
The processing of and regulation through RNA molecules is tightly controlled by RNA binding proteins (RBPs), which bind to RNAs through recognition of sequence and structural motifs and regulate RNA processing in cell-type, condition-specific, or temporal manners.
Recent studies have estimated over 1500 RBPs in the human genome, which play roles throughout the RNA life cycle. Mutation of proper RBP activity has been linked to cancer, Amyotrophic Lateral Sclerosis (ALS), and numerous other diseases, and the emergence of new sequencing techniques will continue to rapidly expand our knowledge of RBPs causally mutated in diseases.
eCLIP-seq builds upon improved library preparation efficiency by nearly one thousand-fold based on much better adapter ligation chemistries. This increases experimental success rates and decreases wasted sequencing due to PCR duplication, see above: 102 eCLIP experiments show lower percentage of PCR duplications, relative to published iCLIP and other CLIP datasets
Transcriptome-wide identification of RNA targets
eCLIP-seq identifies binding sites throughout RNAs, including binding to intronic and exonic positions of coding sequences, 3′ and 5′ untranslated regions, non-coding RNAs including lincRNAs and microRNAs, retrotransposons and other RNA transcripts. See above: Example binding profiles for 5 RBPs
Reverse transcription often terminates at the protein-RNA crosslink site. By performing adapter ligation at the cDNA step, eCLIP can be used to identify binding sites and binding motifs with single-nucleotide resolution, depending on the target protein. See above: Crosslink-termination analysis on RBFOX2
RBP-RNA interactions are covalently linked using UV crosslinking of live cells. Cells are then lysed, and RNA is fragmented using limited RNase treatment. A specific RBP (and its bound RNA) is then immunoprecipitated using an antibody that specifically recognizes the targeted RBP. After ligation of a 3’ RNA adapter, immunoprecipitated material (as well as a paired input sample) are run on denaturing protein gels and transferred to nitrocellulose membranes. A region from the protein size to 75 kDa above is cut from the membrane and treated with Proteinase K to release RNA. After cleanup, RNA is then reverse transcribed to ssDNA, after which a second adapter is ligated. PCR amplification is then used to obtain sufficient material for high-throughput sequencing.