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bioRxiv · 10.1101/2021.08.04.455019

Probing the stability of the SpCas9-DNA complex after cleavage

Aldag, P.·Welzel, F.·Jakob, L.·Schmidbauer, A.·Rutkauskas, M.·Fettes, F.·Grohmann, D.·Seidel, R.
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Abstract

CRISPR-Cas9 is a ribonucleoprotein complex that sequence-specifically binds and cleaves double-stranded DNA. Wildtype Cas9 as well as its nickase and cleavage-incompetent mutants have been used in various biological techniques due to their versatility and programmable specificity. Cas9 has been shown to bind very stably to DNA even after cleavage of the individual DNA strands, inhibiting further turnovers and considerably slowing down in-vivo repair processes. This poses an obstacle in genome editing applications. Here, we employed single-molecule magnetic tweezers to investigate the binding stability of different S. pyogenes Cas9 variants after cleavage by challenging them with supercoiling. We find that different release mechanisms occur depending on which DNA strand is cleaved. After non-target strand cleavage, supercoils are immediately but slowly released by swiveling of the non-target strand around the DNA with friction. Consequently, Cas9 and its non-target strand nicking mutant stay stably bound to the DNA for many hours even at elevated torsional stress. After target-strand cleavage, supercoils are only removed after the collapse of the R-loop. We identified several states with different stabilities of the R-loop. Most importantly, we find that the post-cleavage state of Cas9 exhibits a higher stability compared to the pre-cleavage state. This suggests that Cas9 has evolved to remain tightly bound to its cut target.

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Aldag, P., Welzel, F., Jakob, L., Schmidbauer, A., Rutkauskas, M., Fettes, F., Grohmann, D., Seidel, R.. 2021-08-04. Probing the stability of the SpCas9-DNA complex after cleavage. https://doi.org/10.1101/2021.08.04.455019

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