A novel NIR light-activated CRISPR-dCas9/Cas9 system achieves precise and rapid gene regulation in living organism using a chemically cleavable rapamycin dimer. Unlike previous light-driven systems
this approach offers deeper tissue penetration
low toxicity
fast response
and minimal background activity. This platform opens new directions for highly efficient
targeted
noninvasive
and spatially confined gene editing for a great number of preclinical and clinically translatable applications.
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references
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