Peptides o ni tagata taua i gaioiga o le olaga, ma o latou suiga patino ma fa'ailoga e taua mo le su'esu'eina o latou fausaga ma galuega. Over the past decade, methods have been developed to label glycine on α-carbon. Peitai, these methods require pre-functionalization of glycine, which is not possible for rapid recognition of natural amino acids.In this study, we report the dual activation of the α-methylene of glycine, which distinguishes this glycine from 19 other amino acids.
Technical Advantages
Specific selectivity, utilizing the unique chemical properties of N-terminal glycine to realize its specific reaction with modifying reagents and avoid the interference of other amino acid residues.
- Universal: Applicable to a wide range of N-terminal glycine-containing peptides, as well as different modification groups and fluorescent dyes.
- Wide range of applications: Provide a powerful tool for peptide structure and function studies, drug screening, bio-imaging and other fields.
This study provides a method for selective labeling of N-terminal glycine peptides using 1,3-diphenyl 1,3-diones to provide pyrrole-based fluorescent products. It is strictly selective for N-terminal glycine due to the “dual activation” mechanism. It provides a theoretical basis for customized N-glycine-based fluorescence modification and a stability test method for rapid identification of N-terminal glycine-containing peptides.
