Nucleic acid detection with CRISPR-Cas13a/C2c2
Broad Institute · Harvard University · +6 more institutions
Abstract
Rapid, inexpensive, and sensitive nucleic acid detection may aid point-of-care pathogen detection, genotyping, and disease monitoring. The RNA-guided, RNA-targeting clustered regularly interspaced short palindromic repeats (CRISPR) effector Cas13a (previously known as C2c2) exhibits a "collateral effect" of promiscuous ribonuclease activity upon target recognition. We combine the collateral effect of Cas13a with isothermal amplification to establish a CRISPR-based diagnostic (CRISPR-Dx), providing rapid DNA or RNA detection with attomolar sensitivity and single-base mismatch specificity. We use this Cas13a-based molecular detection platform, termed Specific High-Sensitivity Enzymatic Reporter UnLOCKing…
Citation impact
- FWCI
- 81.18
- Percentile
- 100%
- References
- 36
Authors
19- JSJonathan S. GootenbergCorresponding
Broad Institute, Harvard University, McGovern Institute for Brain Research, Center for Systems Biology, Massachusetts Institute of Technology
- OOOmar O. AbudayyehCorresponding
Broad Institute, McGovern Institute for Brain Research, Massachusetts Institute of Technology
- JWJeong Wook Lee
Harvard University
- PEPatrick Essletzbichler
Broad Institute, McGovern Institute for Brain Research, Massachusetts Institute of Technology
- AJAaron J. Dy
Broad Institute, Massachusetts Institute of Technology
Topics & keywords
- CRISPR
- Recombinase Polymerase Amplification
- Nucleic acid
- Genotyping
- DNA
- Biology
- Computational biology
- Polymerase chain reaction
Funding
- HHHoward Hughes Medical InstituteAward: award301050
- SFSimons FoundationAward: award301051
- PGPaul G. Allen Family FoundationAward: award301054
- NYNew York Stem Cell FoundationAward: award301049
- VFVallee FoundationAward: award301052
- OOOffice of the DirectorAward: award301053
- NONIH Office of the DirectorAwards: award301048, award301047, 5DP1-MH100706, 1R01-MH110049