4.7 Article

Recent trends in glycoproteomics by characterization of intact glycopeptides

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 415, Issue 18, Pages 3727-3738

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-023-04592-z

Keywords

Glycoproteomics; Intact glycopeptides; Enrichment; Protein glycosylation; Quantitative analysis; Qualitative analysis

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This trends article provides an overview of the current state and recent developments in the analysis of intact glycopeptides using LC-MS based proteomics technologies. It covers techniques for sample preparation, characterization of intact glycopeptide structures, and data analysis using bioinformatics. The article also highlights open challenges in the field, including glycopeptide isomerism, quantitative analysis, and characterization of less-studied glycosylation types. Overall, it serves as a valuable resource for researchers in the field and stimulates future research on intact glycopeptide analysis.
This trends article provides an overview of the state of the art in the analysis of intact glycopeptides by proteomics technologies based on LC-MS analysis. A brief description of the main techniques used at the different steps of the analytical workflow is provided, giving special attention to the most recent developments. The topics discussed include the need for dedicated sample preparation for intact glycopeptide purification from complex biological matrices. This section covers the common approaches with a special description of new materials and innovative reversible chemical derivatization strategies, specifically devised for intact glycopeptide analysis or dual enrichment of glycosylation and other post-translational modifications. The approaches are described for the characterization of intact glycopeptide structures by LC-MS and data analysis by bioinformatics for spectra annotation. The last section covers the open challenges in the field of intact glycopeptide analysis. These challenges include the need of a detailed description of the glycopeptide isomerism, the issues with quantitative analysis, and the lack of analytical methods for the large-scale characterization of glycosylation types that remain poorly characterized, such as C-mannosylation and tyrosine O-glycosylation. This bird's-eye view article provides both a state of the art in the field of intact glycopeptide analysis and open challenges to prompt future research on the topic.

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