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Designing a small IscB enzyme to improve precise DNA base editing with wider targeting ability
Updated
Abstract
IminiCBE achieved an average editing efficiency of 67% in mammalian cells.
- IscB has a similar structure to Cas9 but is smaller, making it more suitable for delivery via adeno-associated virus.
- High-efficiency miniature base editors were developed by modifying OgeuIscB and its associated RNA.
- IminiABE demonstrated an average editing efficiency of 52% in mammalian cells.
- The addition of the non-specific DNA-binding protein Sso7d to IminiBEs increased editing efficiency by approximately two- to threefold at low-efficiency sites.
- IminiCBE and SIminiCBE can target a broader range of genomic sites than traditional IscB nickase by recognizing specific motifs.
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