A strategy for Cas13 miniaturization based on the structure and AlphaFold
© 2023. Springer Nature Limited..
The small size of the Cas nuclease fused with various effector domains enables a broad range of function. Although there are several ways of reducing the size of the Cas nuclease complex, no efficient or generalizable method has been demonstrated to achieve protein miniaturization. In this study, we establish an Interaction, Dynamics and Conservation (IDC) strategy for protein miniaturization and generate five compact variants of Cas13 with full RNA binding and cleavage activity comparable the wild-type enzymes based on a combination of IDC strategy and AlphaFold2. In addition, we construct an RNA base editor, mini-Vx, and a single AAV (adeno-associated virus) carrying a mini-RfxCas13d and crRNA expression cassette, which individually shows efficient conversion rate and RNA-knockdown activity. In summary, these findings highlight a feasible strategy for generating downsized CRISPR/Cas13 systems based on structure predicted by AlphaFold2, enabling targeted degradation of RNAs and RNA editing for basic research and therapeutic applications.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:14 |
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Enthalten in: |
Nature communications - 14(2023), 1 vom: 08. Sept., Seite 5545 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Zhao, Feiyu [VerfasserIn] |
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Links: |
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Themen: |
63231-63-0 |
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Anmerkungen: |
Date Completed 11.09.2023 Date Revised 19.11.2023 published: Electronic Citation Status MEDLINE |
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doi: |
10.1038/s41467-023-41320-8 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM361817967 |
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520 | |a The small size of the Cas nuclease fused with various effector domains enables a broad range of function. Although there are several ways of reducing the size of the Cas nuclease complex, no efficient or generalizable method has been demonstrated to achieve protein miniaturization. In this study, we establish an Interaction, Dynamics and Conservation (IDC) strategy for protein miniaturization and generate five compact variants of Cas13 with full RNA binding and cleavage activity comparable the wild-type enzymes based on a combination of IDC strategy and AlphaFold2. In addition, we construct an RNA base editor, mini-Vx, and a single AAV (adeno-associated virus) carrying a mini-RfxCas13d and crRNA expression cassette, which individually shows efficient conversion rate and RNA-knockdown activity. In summary, these findings highlight a feasible strategy for generating downsized CRISPR/Cas13 systems based on structure predicted by AlphaFold2, enabling targeted degradation of RNAs and RNA editing for basic research and therapeutic applications | ||
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700 | 1 | |a Sun, Xiaodi |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Xiyun |e verfasserin |4 aut | |
700 | 1 | |a Chen, Letong |e verfasserin |4 aut | |
700 | 1 | |a Wang, Hejun |e verfasserin |4 aut | |
700 | 1 | |a Li, Jinze |e verfasserin |4 aut | |
700 | 1 | |a Fan, Peng |e verfasserin |4 aut | |
700 | 1 | |a Lai, Liangxue |e verfasserin |4 aut | |
700 | 1 | |a Sui, Tingting |e verfasserin |4 aut | |
700 | 1 | |a Li, Zhanjun |e verfasserin |4 aut | |
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