Structure and specificity of the RNA-guided endonuclease Cas9 during DNA interrogation, target binding and cleavage

Nucleic Acids Res. 2015 Oct 15;43(18):8924-41. doi: 10.1093/nar/gkv892. Epub 2015 Sep 17.

Abstract

CRISPR-associated endonuclease Cas9 cuts DNA at variable target sites designated by a Cas9-bound RNA molecule. Cas9's ability to be directed by single 'guide RNA' molecules to target nearly any sequence has been recently exploited for a number of emerging biological and medical applications. Therefore, understanding the nature of Cas9's off-target activity is of paramount importance for its practical use. Using atomic force microscopy (AFM), we directly resolve individual Cas9 and nuclease-inactive dCas9 proteins as they bind along engineered DNA substrates. High-resolution imaging allows us to determine their relative propensities to bind with different guide RNA variants to targeted or off-target sequences. Mapping the structural properties of Cas9 and dCas9 to their respective binding sites reveals a progressive conformational transformation at DNA sites with increasing sequence similarity to its target. With kinetic Monte Carlo (KMC) simulations, these results provide evidence of a 'conformational gating' mechanism driven by the interactions between the guide RNA and the 14th-17th nucleotide region of the targeted DNA, the stabilities of which we find correlate significantly with reported off-target cleavage rates. KMC simulations also reveal potential methodologies to engineer guide RNA sequences with improved specificity by considering the invasion of guide RNAs into targeted DNA duplex.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Binding Sites
  • CRISPR-Associated Proteins / chemistry*
  • CRISPR-Associated Proteins / metabolism*
  • DNA / metabolism*
  • DNA Cleavage*
  • Endodeoxyribonucleases / chemistry*
  • Endodeoxyribonucleases / metabolism*
  • Humans
  • Microscopy, Atomic Force
  • Protein Binding
  • RNA / chemistry
  • RNA / metabolism

Substances

  • CRISPR-Associated Proteins
  • RNA
  • DNA
  • Endodeoxyribonucleases