Your browser doesn't support javascript.
loading
Photocontrollable Probes for Mitochondrial Protein Profiling.
Guo, Shuhong; Yuan, Chaonan; Lang, Wenjie; Hong, Danqi; Liu, Jian; Huang, Jintao; Dong, Jia; Ge, Jingyan.
Afiliação
  • Guo S; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Chao Wang Road 18, Hangzhou, 310014, P. R. China.
  • Yuan C; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Chao Wang Road 18, Hangzhou, 310014, P. R. China.
  • Lang W; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Chao Wang Road 18, Hangzhou, 310014, P. R. China.
  • Hong D; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Chao Wang Road 18, Hangzhou, 310014, P. R. China.
  • Liu J; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Chao Wang Road 18, Hangzhou, 310014, P. R. China.
  • Huang J; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Chao Wang Road 18, Hangzhou, 310014, P. R. China.
  • Dong J; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Chao Wang Road 18, Hangzhou, 310014, P. R. China.
  • Ge J; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Chao Wang Road 18, Hangzhou, 310014, P. R. China.
Chembiochem ; 23(10): e202200066, 2022 05 18.
Article em En | MEDLINE | ID: mdl-35344259
ABSTRACT
The mitochondrion is the core site of cell signaling, energy metabolism and biosynthesis. Here, taking advantage of activity-based probes, we synthesized two photocontrollable probes (YGH-1 and YGH-2), composed of a mitochondrial localization moiety "triphenylphosphonium", a photo-triggered group to achieve spatially and temporally controlled protein capture, and an alkyne group to enrich the labeled protein. Proteomic validation was further carried out to facilitate identification of the mitochondrial proteome in HeLa cells. The results show that half of the identified protein hits (∼300) labeled by YGH-1 and YGH-2 belong to mitochondria, and are mostly localized in the mitochondrial matrix and inner mitochondrial membrane. Our results provide a new tool for spatial and temporal analysis of subcellular proteomes.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteômica / Mitocôndrias Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteômica / Mitocôndrias Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article