6NME

Structure of LbCas12a-crRNA

Summary for 6NME

• Entry DOI: 10.2210/pdb6nme/pdb
• EMDB information: 0449
• Descriptor: Cpf1, crRNA, MAGNESIUM ION, ... (4 entities in total)
• Functional Keywords: rna, unknown function-rna complex, unknown function/rna
• Biological source: Lachnospiraceae bacterium ND2006; More
• Total number of polymer chains: 2
• Total formula weight: 156678.46

Authors

Chang, L.,Li, Z.,Zhang, H. (deposition date: 2019-01-10, release date: 2019-06-12, Last modification date: 2024-03-20)

Primary citation

Zhang, H.,Li, Z.,Daczkowski, C.M.,Gabel, C.,Mesecar, A.D.,Chang, L.
Structural Basis for the Inhibition of CRISPR-Cas12a by Anti-CRISPR Proteins.
Cell Host Microbe, 25:815-, 2019

PubMed Abstract: CRISPR-Cas12a (Cpf1), a type V CRISPR-associated nuclease, provides bacterial immunity against bacteriophages and plasmids but also serves as a tool for genome editing. Foreign nucleic acids are integrated into the CRISPR locus, prompting transcription of CRISPR RNAs (crRNAs) that guide Cas12a cleavage of foreign complementary DNA. However, mobile genetic elements counteract Cas12a with inhibitors, notably type V-A anti-CRISPRs (AcrVAs). We present cryoelectron microscopy structures of Cas12a-crRNA bound to AcrVA1 and AcrVA4 at 3.5 and 3.3 Å resolutions, respectively. AcrVA1 is sandwiched between the recognition (REC) and nuclease (NUC) lobes of Cas12a and inserts into the binding pocket for the protospacer-adjacent motif (PAM), a short DNA sequence guiding Cas12a targeting. AcrVA1 cleaves crRNA in a Cas12a-dependent manner, inactivating Cas12a-crRNA complexes. The AcrVA4 dimer is anchored around the crRNA pseudoknot of Cas12a-crRNA, preventing required conformational changes for crRNA-DNA heteroduplex formation. These results uncover molecular mechanisms for CRISPR-Cas12a inhibition, providing insights into bacteria-phage dynamics.

PubMed: 31155345
DOI: 10.1016/j.chom.2019.05.004

Experimental method

ELECTRON MICROSCOPY (5.67 Å)