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9I8Y

SpCas12Cas12f1 in complex with sgRNA and cognate DNA

Summary for 9I8Y
Entry DOI10.2210/pdb9i8y/pdb
EMDB information52745
DescriptorCRISPR-associated endodeoxyribonuclease Cas12f1, DNA target strand, DNA non-target strand, ... (5 entities in total)
Functional Keywordscrispr-cas, cas12, cas12f1, rna binding protein
Biological sourceSyntrophomonas palmitatica JCM 14374
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Total number of polymer chains5
Total formula weight198248.55
Authors
Sasnauskas, G.,Baltramonaitis, M.,Karvelis, T.,Siksnys, V. (deposition date: 2025-02-06, release date: 2025-07-23)
Primary citationMadariaga-Marcos, J.,Baltramonaitis, M.,Henkel-Heinecke, S.,Kauert, D.J.,Irmisch, P.,Bigelyte-Stankeviciene, G.,Silanskas, A.,Karvelis, T.,Siksnys, V.,Sasnauskas, G.,Seidel, R.
Structural and mechanistic insights into the sequential dsDNA cleavage by SpCas12f1.
Nucleic Acids Res., 53:-, 2025
Cited by
PubMed Abstract: Miniature CRISPR-Cas12f1 effector complexes have recently attracted considerable interest for genome engineering applications due to their compact size. Unlike other Class 2 effectors, Cas12f1 functions as a homodimer bound to a single ∼200 nt RNA. While the basic biochemical properties of Cas12f1, such as its use of a single catalytic center for catalysis, have been characterized, the orchestration of the different events occurring during Cas12f1 reactions remained little explored. To gain insights into the dynamics and mechanisms involved in DNA recognition and cleavage by Cas12f1 from Syntrophomonas palmitatica (SpCas12f1), we solved the structure of SpCas12f1 bound to target DNA and employed single-molecule magnetic tweezers measurements in combination with ensemble kinetic measurements. Our data indicate that SpCas12f1 forms 18 bp R-loops, in which local contacts of the protein to the R-loop stabilize R-loop intermediates. DNA cleavage is catalyzed by a single SpCas12f1 catalytic center, which first rapidly degrades a ∼11 bp region on the nontarget strand by cutting at random sites. Subsequent target strand cleavage is slower and requires at least a nick in the nontarget strand.
PubMed: 40650969
DOI: 10.1093/nar/gkaf588
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.89 Å)
Structure validation

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