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Site-Specific Profiling of -Glycans in . | LitMetric

Site-Specific Profiling of -Glycans in .

Front Biosci (Landmark Ed)

College of Basic Medical Sciences, Shaanxi University of Chinese Medicine, 712046 Xianyang, Shaanxi, China.

Published: November 2023

Background: is a well-studied and highly tractable genetic model system for deciphering the molecular mechanisms underlying various biological processes. Although being one of the most critical post-translational modifications of proteins, the understanding of glycosylation in is still lagging behind compared with that of other model organisms.

Methods: In this study, we systematically investigated the site-specific -glycan profile of using intact glycopeptide analysis technique. This approach identified the glycans, proteins, and their glycosites in , as well as information on site-specific glycosylation, which allowed us to know which glycans are attached to which glycosylation sites.

Results: The results showed that the majority of -glycans in were high-mannose type (69.3%), consistent with reports in other insects. Meanwhile, fucosylated -glycans were also highly abundant (22.7%), and the majority of them were mono-fucosylated. In addition, 24 different sialylated glycans attached with 16 glycoproteins were identified, and these proteins were mainly associated with developmental processes. Gene ontology analysis showed that -glycosylated proteins in were involved in multiple biological processes, such as axon guidance, N-linked glycosylation, cell migration, cell spreading, and tissue development. Interestingly, we found that seven glycosyltransferases and four glycosidases were -glycosylated, which suggested that -glycans may play a regulatory role in the synthesis and degradation of -glycans and glycoproteins.

Conclusions: To our knowledge, this work represents the first comprehensive analysis of site-specific -glycosylation in , thereby providing new perspectives for the understanding of biological functions of glycosylation in insects.

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Source
http://dx.doi.org/10.31083/j.fbl2811278DOI Listing

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