Adenoviral Delivery of CRISPR/Cas9 Aims to Expand Genome Editing to Primary Cells
Type
Blog Post
Published
Dec. 10, 2020, 1 p.m.
...vectors (right) are transduced to target cells. Within target cells, Cas9 machinery is transiently expressed...in order to facilitate its entry into the target cells (Beatty et al., 2012). These features make AdV an... complexes into transformed and non-transformed cells yielded rates of targeted mutagenesis similar to...nuclease-induced gene disruption frequencies in the various cell types ranged from 18% to 65% (Maggio et al., 2014... leads to a vast majority of AdV-modified human cells being subjected to scarless homology-directed genome...therapeutically relevant, non-transformed mammalian cells. These viral vector systems also work equally well... dividing and quiescent, post-mitotic mammalian cells.
Applications of CRISPR delivery by adenoviral ...