Author

Chaoshuang Xia

Boston UniversityORCID 0000-0001-7076-4813Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Approach:experimental assay· 3 Organism:human· 2 Assay:proteomics· 2 Organism:C. elegans· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

Catherine E. CostelloiD· 2 shared Avital Adah RodaliD· 1 shared Barbara ImperialiiD· 1 shared Bing XuiD· 1 shared Cheng Lin· 1 shared Christine A. ArbouriD· 1 shared Daniela M. DinulescuiD· 1 shared David Mark LoebiD· 1 shared

Activity by Year

2026-2026 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersImmunology

Catherine E. CostelloORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

ImmunologybioRxivPreprintOct 14, 2026

The Human Contraceptive Antibody Targets A Semenogelin Galectin-3 N-Linked Glycan Complex on the Sperm Surface

Sarah Dohadwala, Chaoshuang Xia, Shane Finn…·Deborah Jean Anderson

This paper identifies the HCA antibody's target as a semenogelin-galectin-3 complex on the sperm surface, rather than CD52, through affinity purification and glycan analysis.

DOI 10.64898/2026.10.13.757762

humanproteomics

𝕏 PostBluesky

BiochemistryJournal of Biological ChemistryPeer-reviewedOct 1, 2026

Glycoconjugate diversification in Campylobacter concisus is determined by two glycosyltransferases

Hayley L. Knox, Christine A. Arbour, Chaoshuang Xia…·Karen N. Allen

The paper identifies the final N-linked glycan structure in Campylobacter concisus and reveals the roles of two glycosyltransferases in its diversification.

DOI 10.1016/j.jbc.2026.113704

C. elegansproteomics

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BiochemistryNature CommunicationsPeer-reviewedJan 28, 2026

Cycling Molecular Assemblies for Selective Cancer Cell Golgi Disruption

Weiyi Tan, Qiuxin Zhang, Zhiyu Liu…·Bing Xu

This paper develops CyMA, small peptides that disrupt cancer cell Golgi function by exploiting enzymatic cycles, showing selectivity over hepatocytes and immune cells.

6 citations

humanexperimental assay

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