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Lamberth, J.

Publications and source records attributed to Lamberth, J..

2 recordsLinked to original sources

TFU72 is a novel and potent DNA-PKcs inhibitor for enhancing homology-directed repair gene editing

Precise gene editing through homology directed repair (HDR) is one of the most versatile genome editing approaches with broad applications. Achieving high HDR gene editing efficiency is critical to realizing the full potential of this approach. Although many strategies have been explored to enhance HDR editing efficiency, inhibition of DNA-dependent protein kinase catalytic subunit (DNA-PKcs), a key component of the non-homologous end joining (NHEJ) pathway remains one of the most effective. Here we describe a novel, highly potent DNA-PKcs small molecule inhibitor, TFU72 which enhances HDR gene editing efficiency remarkably by up to 30-fold in cell lines and human primary cells. We assessed the previously reported genotoxic outcomes associated with DNA-PKcs inhibition such as off-target mutations, chromosomal translocations and large deletions and describe approaches to mitigate these outcomes to safely enhance HDR gene editing efficiency with TFU72. This optimized approach enables broad application of TFU72 for HDR-based precise gene editing applications in both therapeutic and research settings.

molecular biology↗

Highly efficient and specific genome editing in human cells with paired CRISPR-Cas9 nickase ribonucleoproteins

CRISPR technology has opened up many diverse genome editing possibilities in human somatic cells, but has been limited in the therapeutic realm by both potential off-target effects and low genome modification efficiencies. Recent advancements to combat these limitations include delivering Cas9 nucleases directly to cells as highly purified ribonucleoproteins (RNPs) instead of the conventional plasmid DNA and RNA-based approaches. Here, we extend RNP-based delivery in cell culture to a less characterized CRISPR format which implements paired Cas9 nickases. The use of paired nickase Cas9 RNP system, combined with a GMP-compliant non-viral delivery technology, enables editing in human cells with high specificity and high efficiency, a development that opens up the technology for further exploration into a more therapeutic role.

molecular biology↗