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A thiol-selective and acid-stable protein modification strategy using an electron-deficient yne reagent.
Chen, Zhi-Liang; Chen, Wen; Wang, Fenglin; Jiang, Jian-Hui; Dong, Wan-Rong.
Afiliação
  • Chen ZL; State Key Laboratory of Chemo/Biosensing & Chemometrics, College of Chemistry & Chemical Engineering, Hunan University, Changsha 410082, China. wanrongdong@hnu.edu.cn.
  • Chen W; School of Pharmacy, Shaoyang University, Shaoyang, 422000, P. R China.
  • Wang F; State Key Laboratory of Chemo/Biosensing & Chemometrics, College of Chemistry & Chemical Engineering, Hunan University, Changsha 410082, China. wanrongdong@hnu.edu.cn.
  • Jiang JH; State Key Laboratory of Chemo/Biosensing & Chemometrics, College of Chemistry & Chemical Engineering, Hunan University, Changsha 410082, China. wanrongdong@hnu.edu.cn.
  • Dong WR; State Key Laboratory of Chemo/Biosensing & Chemometrics, College of Chemistry & Chemical Engineering, Hunan University, Changsha 410082, China. wanrongdong@hnu.edu.cn.
Org Biomol Chem ; 22(36): 7311-7315, 2024 09 18.
Article em En | MEDLINE | ID: mdl-39163001
ABSTRACT
A protein modification strategy was developed based on a thiol-yne click reaction using an electron-deficient yne reagent. This approach demonstrated exceptional selectivity towards thiols and exhibited rapid kinetics, resulting in conjugates with superior acid stability. The conjugation of IgG with an indole-derived fluorophore was achieved for the imaging of PD-L1 in cancer cells.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Sulfidrila / Elétrons / Química Click Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Sulfidrila / Elétrons / Química Click Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article