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TitleImproving the efficiency of high-fidelity Cas9 by enhancing PAM-distal interactions.
Journal, issue, pagesNat Struct Mol Biol, Year 2026
Publish dateMar 18, 2026
AuthorsRong Zheng / Zhike Lu / Rongwei Wei / Young-Cheul Shin / Jiang Du / Qingfeng Zhang / Jianbo Li / Xiaoqi Wang / Yi Wei / Botao Liu / Yang Chen / Lihong Ding / Heng Zhang / Hui Chen / Jing Huang / Lijia Ma /
PubMed AbstractEngineering CRISPR enzymes for high fidelity often impairs cleavage activity. Meanwhile, a mechanistic understanding of why high-fidelity mutations reduce Cas9's cleavage activity remains unclear, ...Engineering CRISPR enzymes for high fidelity often impairs cleavage activity. Meanwhile, a mechanistic understanding of why high-fidelity mutations reduce Cas9's cleavage activity remains unclear, presenting a challenge in balancing nuclease specificity and efficiency for clinical applications. In this study, we show that extending the spacer region to 21 or 22 nucleotides restores the impaired cleavage activity of SuperFi-Cas9, a high-fidelity Cas9 variant with 7 mutations in the RuvC domain at the protospacer adjacent motif (PAM)-distal region. Cryo-electron microscopy structures and mutational analyses reveal that the negatively charged mutations in a protruding loop of the RuvC domain create repulsive forces that destabilize the nuclease-single guide (sg)RNA-DNA complex. Spacer extension enhances interactions in the PAM-distal region, effectively restoring cleavage activity and balancing editing efficiency with specificity. In addition, we develop a deep learning model, AIdit-SuperFi, to predict optimal sgRNA length for high-fidelity genome editing. Our findings introduce a straightforward strategy to enhance CRISPR complex stability and provide mechanistic insights into the impaired cleavage activity of engineered high-fidelity Cas9, presenting a pathway toward precise and efficient genome editing and clinical translation of CRISPR technologies.
External linksNat Struct Mol Biol / PubMed:41851507
MethodsEM (single particle)
Resolution3.79 - 4.4 Å
Structure data

EMDB-65730, PDB-9w7q:
SuperFi Cas9 - 20nt sgRNA - DNA ternary complex Class A
Method: EM (single particle) / Resolution: 3.79 Å

EMDB-65732, PDB-9w7t:
SuperFi Cas9 - 20nt sgRNA - DNA ternary complex Class B
Method: EM (single particle) / Resolution: 3.91 Å

EMDB-65733, PDB-9w7u:
SuperFi Cas9 - 20nt sgRNA - DNA ternary complex Class C
Method: EM (single particle) / Resolution: 3.83 Å

EMDB-65734, PDB-9w7v:
SuperFi Cas9 - 20nt sgRNA - DNA ternary complex Class D
Method: EM (single particle) / Resolution: 3.81 Å

EMDB-65771, PDB-9w9d:
SuperFi Cas9 - 22nt sgRNA - DNA ternary complex
Method: EM (single particle) / Resolution: 4.4 Å

EMDB-65809, PDB-9wa9:
SuperFi Cas9 - 22nt sgRNA - DNA ternary complex Class B
Method: EM (single particle) / Resolution: 4.12 Å

EMDB-65810, PDB-9waa:
SuperFi Cas9 - 22nt sgRNA - DNA ternary complex Class C
Method: EM (single particle) / Resolution: 4.17 Å

EMDB-65827, PDB-9waw:
SuperFi Cas9 - 20nt sgRNA - DNA ternary complex Class E
Method: EM (single particle) / Resolution: 3.95 Å

Source
  • streptococcus pyogenes (bacteria)
  • streptococcus pyogenes serotype m1 (bacteria)
  • synthetic construct (others)
KeywordsIMMUNE SYSTEM / Complex / cas / SuperFi cas9

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