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  Chimeric CRISPR-CasX enzymes and guide RNAs for improved genome editing activity

Tsuchida, C. A., Zhang, S., Doost, M. S., Zhao, Y., Wang, J., O'Brien, E., et al. (2022). Chimeric CRISPR-CasX enzymes and guide RNAs for improved genome editing activity. Molecular Cell, 82(6), 1199-1209.e6. doi:10.1016/j.molcel.2022.02.002.

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 Urheber:
Tsuchida, Connor A.1, Autor
Zhang, Shouyue1, Autor
Doost, Mohammad Saffari1, Autor
Zhao, Yuqian1, Autor
Wang, Jia1, Autor
O'Brien, Elizabeth1, Autor
Fang, Huan1, Autor
Li, Cheng-Ping1, Autor
Li, Danyuan1, Autor
Hai, Zhuo-Yan1, Autor
Chuck, Jonathan1, Autor
Brötzmann, Julian2, Autor           
Vartoumian, Araz1, Autor
Burstein, David1, Autor
Chen, Xiao-Wei1, Autor
Nogales, Eva1, Autor
Doudna, Jennifer A.1, Autor
Liu, Jun-Jie Gogo1, Autor
Affiliations:
1external, ou_persistent22              
2Conti, Elena / Structural Cell Biology, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565144              

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Schlagwörter: RECOGNITION; CLEAVAGE; BIOLOGY; SYSTEMSBiochemistry & Molecular Biology; Cell Biology;
 Zusammenfassung: A compact protein with a size of <1,000 amino acids, the CRISPR-associated protein CasX is a fundamentally distinct RNA-guided nuclease when compared to Cas9 and Cas12a. Although it can induce RNA-guided genome editing in mammalian cells, the activity of CasX is less robust than that of the widely used S. pyogenes Cas9. Here, we show that structural features of two CasX homologs and their guide RNAs affect the R-loop complex assembly and DNA cleavage activity. Cryo-EM-based structural engineering of either the CasX protein or the guide RNA produced two new CasX genome editors (DpbCasX-R3-v2 and PlmCasX-R1v2) with significantly improved DNA manipulation efficacy. These results advance both the mechanistic understanding of CasX and its application as a genome-editing tool.

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Sprache(n): eng - English
 Datum: 2022
 Publikationsstatus: Erschienen
 Seiten: 18
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: ISI: 000773302500002
DOI: 10.1016/j.molcel.2022.02.002
 Art des Abschluß: -

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Titel: Molecular Cell
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Cambridge, Mass. : Cell Press
Seiten: - Band / Heft: 82 (6) Artikelnummer: - Start- / Endseite: 1199 - 1209.e6 Identifikator: ISSN: 1097-2765
CoNE: https://pure.mpg.de/cone/journals/resource/954925610929