Dynamics changes of CRISPR-Cas9 systems induced by high fidelity mutations

CRISPR-Cas9, a powerful genome editing tool, has widely been applied in biological fields. Since the discovery of CRISPR-Cas9 as an adaptive immune system, it has been gradually modified to perform precise genome editing in eukaryotic cells by creating double-strand breaks. Although it is robust and...

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Main Authors: Zheng, Liangzhen, Shi, Jiahai, Mu, Yuguang
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/139057
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1390572023-02-28T17:10:20Z Dynamics changes of CRISPR-Cas9 systems induced by high fidelity mutations Zheng, Liangzhen Shi, Jiahai Mu, Yuguang School of Biological Sciences Science::Physics Mutations Cas9 CRISPR-Cas9, a powerful genome editing tool, has widely been applied in biological fields. Since the discovery of CRISPR-Cas9 as an adaptive immune system, it has been gradually modified to perform precise genome editing in eukaryotic cells by creating double-strand breaks. Although it is robust and efficient, the current CRISPR-Cas9 system faces a major flaw: off-target effects, which are not well understood. Several Cas9 mutants show significant improvement, with very low off-target effects; however, they also show relatively lower cleavage efficiency for on-target sequences. In this study, the dynamics of wild-type Cas9 from Streptococcus pyogenes and a high fidelity Cas9 mutant have been explored using molecular dynamics simulations. It was found that the mutations cause decreased electrostatic interactions between Cas9 and the R-loop. Consequently, the flexibility of the tDNA/sgRNA heteroduplex is decreased, which may explain the lower tolerance of mismatches in the heteroduplex region. The mutations also affect the protein dynamics and the correlation networks among Cas9 domains. In mutant Cas9, weakened communications between two catalytic domains as well as a slight opening of the conformation induced by the mutations account for the lower on-target cleavage efficiency and probably the lower off-target efficiency as well. These findings will facilitate more precise Cas9 engineering in future. MOE (Min. of Education, S’pore) Accepted version 2020-05-15T03:41:08Z 2020-05-15T03:41:08Z 2018 Journal Article Zheng, L., Shi, J., & Mu, Y. (2018). Dynamics changes of CRISPR-Cas9 systems induced by high fidelity mutations. Physical Chemistry Chemical Physics, 20(43), 27439-27448. doi:10.1039/C8CP04226H 1463-9076 https://hdl.handle.net/10356/139057 10.1039/C8CP04226H 43 20 27439 27448 en Physical Chemistry Chemical Physics © 2018 The Owner Societies. All rights reserved. This paper was published by Royal Society of Chemistry in Physical Chemistry Chemical Physics and is made available with permission of The Owner Societies. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Physics
Mutations
Cas9
spellingShingle Science::Physics
Mutations
Cas9
Zheng, Liangzhen
Shi, Jiahai
Mu, Yuguang
Dynamics changes of CRISPR-Cas9 systems induced by high fidelity mutations
description CRISPR-Cas9, a powerful genome editing tool, has widely been applied in biological fields. Since the discovery of CRISPR-Cas9 as an adaptive immune system, it has been gradually modified to perform precise genome editing in eukaryotic cells by creating double-strand breaks. Although it is robust and efficient, the current CRISPR-Cas9 system faces a major flaw: off-target effects, which are not well understood. Several Cas9 mutants show significant improvement, with very low off-target effects; however, they also show relatively lower cleavage efficiency for on-target sequences. In this study, the dynamics of wild-type Cas9 from Streptococcus pyogenes and a high fidelity Cas9 mutant have been explored using molecular dynamics simulations. It was found that the mutations cause decreased electrostatic interactions between Cas9 and the R-loop. Consequently, the flexibility of the tDNA/sgRNA heteroduplex is decreased, which may explain the lower tolerance of mismatches in the heteroduplex region. The mutations also affect the protein dynamics and the correlation networks among Cas9 domains. In mutant Cas9, weakened communications between two catalytic domains as well as a slight opening of the conformation induced by the mutations account for the lower on-target cleavage efficiency and probably the lower off-target efficiency as well. These findings will facilitate more precise Cas9 engineering in future.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Zheng, Liangzhen
Shi, Jiahai
Mu, Yuguang
format Article
author Zheng, Liangzhen
Shi, Jiahai
Mu, Yuguang
author_sort Zheng, Liangzhen
title Dynamics changes of CRISPR-Cas9 systems induced by high fidelity mutations
title_short Dynamics changes of CRISPR-Cas9 systems induced by high fidelity mutations
title_full Dynamics changes of CRISPR-Cas9 systems induced by high fidelity mutations
title_fullStr Dynamics changes of CRISPR-Cas9 systems induced by high fidelity mutations
title_full_unstemmed Dynamics changes of CRISPR-Cas9 systems induced by high fidelity mutations
title_sort dynamics changes of crispr-cas9 systems induced by high fidelity mutations
publishDate 2020
url https://hdl.handle.net/10356/139057
_version_ 1759854597524946944