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Curr Gene Ther · 2017

CRISPR/Cas9 Editing to Facilitate and Expand Drug Discovery.

Current gene therapy, 17(4): 275-285 PMID 29173168 DOI 10.2174/1566523217666171121164615

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Abstract

INTRODUCTIONThe ability of most laboratories to easily access CRISPR/Cas9 engineering tools has caused a revolution in biology. One of the areas that will continue to be impacted by genome editing is the drug discovery process.

OBJECTIVECRISPR/Cas9 will not only serve to accelerate the drug discovery pipeline, but also streamline line it by identifying high-value targets, facilitating the validation of drug: target interactions and mechanisms of action, and stimulating the development of phenotype-based high throughput screens as alternatives to target-based assays.

CONCLUSIONWe review the literature and hurdles that have been overcome to develop the current generation of tools being used to enrich the drug discovery paradigm.

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