CRISPR-Cas12a detection of DNA glycosylases


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
10 Oct 2024
Historique:
medline: 10 10 2024
pubmed: 10 10 2024
entrez: 10 10 2024
Statut: aheadofprint

Résumé

A programmable CRISPR-Cas12a system for selective detection of various DNA glycosylases is described. By temporarily inactivating Cas12a through the introduction of specific DNA modifications in the complementary DNA strand of Cas12a's crRNA, the system is able to detect the target DNA glycosylases. This approach addresses critical gaps in current CRISPR-Cas12a diagnostics for non-nucleic acid detection beyond the limitations of aptamers.

Identifiants

pubmed: 39385597
doi: 10.1039/d4cc04180a
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Youxian Li (Y)

Guangdong Provincial Key Laboratory of Digestive Cancer Research, Digestive Diseases Center, Scientific Research Center, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, Guangdong, 518107, P. R. China. wangjq97@mail.sysu.edu.cn.

Xiaoquan Yang (X)

School of Medicine, Sun Yat-sen University, Shenzhen, Guangdong, 518107, P. R. China.

Yi Dong (Y)

School of Medicine, Sun Yat-sen University, Shenzhen, Guangdong, 518107, P. R. China.

Jiaqi Wang (J)

Guangdong Provincial Key Laboratory of Digestive Cancer Research, Digestive Diseases Center, Scientific Research Center, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, Guangdong, 518107, P. R. China. wangjq97@mail.sysu.edu.cn.

Chaoxing Liu (C)

Guangdong Provincial Key Laboratory of Digestive Cancer Research, Digestive Diseases Center, Scientific Research Center, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, Guangdong, 518107, P. R. China. wangjq97@mail.sysu.edu.cn.

Classifications MeSH