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New modified CRISPR protein can fit inside virus used for gene therapy

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Researchers have developed a novel version of a key CRISPR gene-editing protein that shows efficient editing activity and is small enough to be packaged within a non-pathogenic virus that can deliver it to target cells. Hongjian Wang and colleagues at Wuhan University, China, present these findings in the open-access journal PLOS Biology.

New modified CRISPR protein can fit inside virus used for gene therapy retrieved 30 May 2024 from https://phys.org/news/2024-05-crispr-protein-virus-gene-therapy.html

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