4.8 Article

High-Resolution Structure of Cas13b and Biochemical Characterization of RNA Targeting and Cleavage

Journal

CELL REPORTS
Volume 26, Issue 13, Pages 3741-+

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2019.02.094

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Funding

  1. Paul and Daisy Soros Fellowship
  2. NIH [F30 NRSA 1F30-CA210382, 1R01-HG009761, 1R01-MH110049, 1DP1-HL141201]
  3. Howard Hughes Medical Institute
  4. New York Stem Cell Foundation
  5. Simons Foundation
  6. Paul G. Allen Family Foundation
  7. Vallee Foundation
  8. Poitras Center for Affective Disorders Research at MIT
  9. Hock E. Tan and K. Lisa Yang Center for Autism Research at MIT
  10. Novo Nordisk Foundation [NNF14CC0001]
  11. cryoEM grant [NNF0024386]
  12. cryoNET grant [NNF17SA0030214]

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Type VI CRISPR-Cas systems contain programmable single-effector RNA-guided RNases, including Cas13b, one of the four known family members. Cas13b, which has been used for both RNA editing and nucleic acid detection, is unique among type VI CRISPR effectors in its linear domain architecture and CRISPR RNA (crRNA) structure. Here, we report the crystal structure of Prevotella buccae Cas13b (PbuCas13b) bound to crRNA at 1.65 angstrom resolution. This structure, combined with biochemical experiments assaying the stability, kinetics, and function of Cas13b, provides a mechanistic model for Cas13b target RNA recognition and identifies features responsible for target and cleavage specificity. Based on these observations, we generated Cas13b variants with altered cleavage preferences, which may expand the utility of nuclease-based RNA detection assays and other applications of Cas13b in mammalian cells.

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