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The application of genome-wide CRISPR-Cas9 screens to dissect the molecular mechanisms of toxins.
Wang, Bei; Chen, Jun-Zhu; Luo, Xue-Qun; Wan, Guo-Hui; Tang, Yan-Lai; Wang, Qiao-Ping.
Afiliación
  • Wang B; Lab of Metabolism and Aging, School of Pharmaceutical Sciences (Shenzhen), Sun Yat-sen University, Shenzhen 518107, PR China.
  • Chen JZ; Department of Pediatrics, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, Guangdong Province, PR China.
  • Luo XQ; Department of Pediatrics, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, Guangdong Province, PR China.
  • Wan GH; School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510275, PR China.
  • Tang YL; Department of Pediatrics, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, Guangdong Province, PR China.
  • Wang QP; Lab of Metabolism and Aging, School of Pharmaceutical Sciences (Shenzhen), Sun Yat-sen University, Shenzhen 518107, PR China.
Comput Struct Biotechnol J ; 20: 5076-5084, 2022.
Article en En | MEDLINE | ID: mdl-36187925
ABSTRACT
Many toxins are life-threatening to both animals and humans. However, specific antidotes are not available for most of those toxins. The molecular mechanisms underlying the toxicology of well-known toxins are not yet fully characterized. Recently, the advance in CRISPR-Cas9 technologies has greatly accelerated the process of revealing the toxic mechanisms of some common toxins on hosts from a genome-wide perspective. The high-throughput CRISPR screen has made it feasible to untangle complicated interactions between a particular toxin and its corresponding targeting tissue(s). In this review, we present an overview of recent advances in molecular dissection of toxins' cytotoxicity by using genome-wide CRISPR screens, summarize the components essential for toxin-specific CRISPR screens, and propose new strategies for future research.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Comput Struct Biotechnol J Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Comput Struct Biotechnol J Año: 2022 Tipo del documento: Article