Dinitroimidazoles as bifunctional bioconjugation reagents for protein functionalization and peptide macrocyclization
The selective formation of protein bioconjugates under physiological conditions is a challenging task. Here, the authors report that 1,4-dinitroimidazoles are reagents of choice for protein bioconjugation at either cysteine or lysine sites within short times and provide facile access to peptide macr...
Main Authors: | Qunfeng Luo, Youqi Tao, Wangjian Sheng, Jingxia Lu, Huan Wang |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2019-01-01
|
Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-018-08010-2 |
Similar Items
-
Organometallic Palladium Reagents for Polypeptide Bioconjugation and Macrocyclization
by: Mallek, Aaron J.
Published: (2022) -
Palladium reagents for bioconjugation
by: Rojas, Anthony J. (Anthony Jose)
Published: (2019) -
Organometallic palladium reagents for cysteine bioconjugation
by: Vinogradova, Ekaterina V., et al.
Published: (2017) -
Silicon-containing thiol-specific bioconjugating reagent
by: Zhang, Zhenguo, et al.
Published: (2024) -
Peptide-guided functionalization and macrocyclization of bioactive peptidosulfonamides by Pd(II)-catalyzed late-stage C–H activation
by: Jian Tang, et al.
Published: (2018-08-01)