Chemical control of 2'-hydroxyl-dependent Cas9 target engagement enables CRISPR RNA ribose replacement

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Authors: Adrian A Pater, Halle M Barber, Sruthi Sudhakar, Ramadevi Chilamkurthy, Sunit K Jana, Mansi A Parasrampuria, Michael S. Bosmeny, Jacob A Graczyk-Marrs, Seth B Eddington, Cole A Blazier, Leonora Abdullahu, Elise Malek-Adamian
+6 more Christopher L Barkau, Daniel O’Reilly, Sergey Korolev, P I Pradeepkumar, Masad José Damha, Keith T. Gagnon
Cited by: 1

Abstract

Advanced CRISPR-based therapies benefit from CRISPR RNA (crRNA) with high nuclease resistance and enhanced drug-like properties, which is primarily achieved through chemical replacement of the RNA ribose moiety. However, for gene editing enzymes like CRISPR-Cas9 a handful of residues cannot be replaced with chemical ribose analogues, limiting the scope of therapeutic strategies. The mechanism underlying this restriction has remained unclear. Here, using nucleic acid chemistry, biochemistry, cryo-EM, and molecular dynamics simulations, we show that the ribose 2'-hydroxyl group at specific crRNA residues is required to achieve a conformational state competent for Cas9 target DNA binding. Based on the mechanistic principles uncovered, we combined site-specific phosphorothioate linkage chemistry with ribose replacement chemistry to restore binding and activity, resulting in high Cas9 editing efficiency and fidelity with a ribose-free crRNA. This study offers novel mechanistic insight and crRNAs with full chemical stabilization, making rational design of guide RNAs with complete nuclease protection for CRISPR-based medicines possible.

Fields of Study & Subjects

CRISPR and Genetic Engineering RNA regulation and disease PARP inhibition in cancer therapy

Publication details

Journal / source
bioRxiv (Cold Spring Harbor Laboratory)
Publisher
openRxiv
Publication date
26 January 2026
Language
EN
Document type
Preprint