| Literature DB >> 33915022 |
Tsung-Shing Andrew Wang1, Ruo-Yu Wu1, Yu Hong1, Zhe-Chong Wang2, Tsung-Lin Li2, Jiun-Jie Shie3, Cheng-Chih Hsu1.
Abstract
Secondary metabolites are structurally diverse natural products (NPs) and have been widely used for medical applications. Developing new tools to enrich NPs can be a promising solution to isolate novel NPs from the native and complex samples. Here, we developed native and deuterated chemoselective labeling probes to target phenol-containing glycopeptides by the ene-type labeling used in proteomic research. The clickable azido-linker was included for further biotin functionalization to facilitate the enrichment of labeled substrates. Afterward, our chemoselective method, in conjunction with LC-MS and MSn analysis, was demonstrated in bacterial cultures. A vancomycin-related phenol-containing glycopeptide was labeled and characterized by our labeling strategy, showing its potential in glycopeptide discovery in complex environments.Entities:
Keywords: chemoselective probe; glycopeptide; isotope tag; secondary metabolite; vancomycin
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Year: 2021 PMID: 33915022 DOI: 10.1002/cbic.202100169
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164