A thermostable Cas9 with increased lifetime in human plasma

Lucas B. Harrington, David Paez-Espino, Brett T. Staahl, Janice S. Chen, Enbo Ma, Nikos C. Kyrpides and Jennifer A. Doudna ()
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Lucas B. Harrington: University of California
David Paez-Espino: Joint Genome Institute
Brett T. Staahl: University of California
Janice S. Chen: University of California
Enbo Ma: University of California
Nikos C. Kyrpides: Joint Genome Institute
Jennifer A. Doudna: University of California

Nature Communications, 2017, vol. 8, issue 1, 1-8

Abstract: Abstract CRISPR-Cas9 is a powerful technology that has enabled genome editing in a wide range of species. However, the currently developed Cas9 homologs all originate from mesophilic bacteria, making them susceptible to degradation and unsuitable for applications requiring cleavage at elevated temperatures. Here, we show that the Cas9 protein from the thermophilic bacterium Geobacillus stearothermophilus (GeoCas9) catalyzes RNA-guided DNA cleavage at elevated temperatures. GeoCas9 is active at temperatures up to 70 °C, compared to 45 °C for Streptococcus pyogenes Cas9 (SpyCas9), which expands the temperature range for CRISPR-Cas9 applications. We also found that GeoCas9 is an effective tool for editing mammalian genomes when delivered as a ribonucleoprotein (RNP) complex. Together with an increased lifetime in human plasma, the thermostable GeoCas9 provides the foundation for improved RNP delivery in vivo and expands the temperature range of CRISPR-Cas9.

Date: 2017
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DOI: 10.1038/s41467-017-01408-4

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