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| Title | Structural basis of AtCas9 recognition of PAM mutants in underwound DNA topology. |
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| Journal, issue, pages | Nat Struct Mol Biol, Vol. 33, Issue 7, Page 1062-1074, Year 2026 |
| Publish date | Jun 24, 2026 |
Authors | Min Duan / Bing Meng / Lei Zhou / Lijie Wu / Xiaohan Tong / Dongchao Huang / Hao Yin / Zhi-Jie Liu / Ying Zhang / ![]() |
| PubMed Abstract | The CRISPR-Cas9 system locates targets through guide RNA pairing and recognition of a protospacer-adjacent motif (PAM). Although PAM specificity is sequence-determined, DNA topology can relax PAM ...The CRISPR-Cas9 system locates targets through guide RNA pairing and recognition of a protospacer-adjacent motif (PAM). Although PAM specificity is sequence-determined, DNA topology can relax PAM requirements and enable near-PAMless cleavage by the type II-C Alicyclobacillus tengchongensis Cas9 (AtCas9). However, the structural mechanism underlying this regulation remains unknown. Here we report cryogenic-electron microscopy (cryo-EM) structures of AtCas9 bound to B-form DNA or a 340 bp underwound minicircle DNA containing wild-type or mutant PAMs. Despite PAM sequences differences, all three underwound complexes adopt an almost identical architecture distinct from the B-form DNA-bound state. On B-form DNA, AtCas9 recognizes the PAM through base-specific hydrogen bonds and steric exclusion, conferring preference for NCNNN and NRNNA (R = A/G). By contrast, underwound DNA widens the PAM major groove and promotes sequence-independent backbone contacts, explaining the near-PAMless cleavage. These findings uncover a topology-dependent mechanism of PAM recognition and establish a cryo-EM platform using underwound minicircle DNA for structural studies under native-like topological states. |
External links | Nat Struct Mol Biol / PubMed:42342973 |
| Methods | EM (single particle) |
| Resolution | 2.41 - 3.15 Å |
| Structure data | EMDB-65811, PDB-9wac: EMDB-65812, PDB-9wad: EMDB-67605, PDB-21dz: EMDB-67606, PDB-21ea: |
| Source |
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Keywords | RNA BINDING PROTEIN/RNA/DNA / Complex / Endonuclease / Immunity / RNA BINDING PROTEIN-RNA-DNA complex |
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Alicyclobacillus tengchongensis (bacteria)
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