| Literature DB >> 31943634 |
Cody M Palumbo1, Jeton M Gutierrez-Bujari1, Henriette O'Geen2, David J Segal2, Peter A Beal1.
Abstract
Specific applications of CRISPR/Cas genome editing systems benefit from chemical modifications of the sgRNA. Herein we describe a versatile and efficient strategy for functionalization of the 3'-end of a sgRNA. An exemplary collection of six chemically modified sgRNAs was prepared containing crosslinkers, a fluorophore and biotin. Modification of the sgRNA 3'-end was broadly tolerated by Streptococcus pyogenes Cas9 in an in vitro DNA cleavage assay. The 3'-biotinylated sgRNA was used as an affinity reagent to identify IGF2BP1, YB1 and hnRNP K as sgRNA-binding proteins present in HEK293T cells. Overall, the modification strategy presented here has the potential to expand on current applications of CRISPR/Cas systems.Entities:
Keywords: RNA; click chemistry; nucleic acids; protein engineering; proteomics
Mesh:
Substances:
Year: 2020 PMID: 31943634 PMCID: PMC7323579 DOI: 10.1002/cbic.201900736
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164