High-fidelity genome and prime editing enabled by the AI-designed openCRISPR-1

Summary

These findings establish generative AI-guided protein design as a powerful strategy to overcome the specificity-efficiency trade-off, expanding the genome editing toolkit for both research and therapeutic use, and ushering in a new era of rational protein design. © 2026. The Author(s).

Authors Hwang HY, Yi H, Gwon Y, Jeon E, Kim D
Journal Genome medicine
Publication Date 2026 May 26;18(1)
PubMed 42192532
PubMed Central PMC13393691
DOI 10.1186/s13073-026-01682-2

Research Projects

Cell Lines