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Direct discrimination of cell surface glycosylation signatures using a single pH-responsive boronic acid-functionalized polymer

Cell surface glycans serve fundamental roles in many biological processes, including cell–cell interaction, pathogen infection, and cancer metastasis. Cancer cell surface have alternative glycosylation to healthy cells, making these changes useful hallmarks of cancer. However, the diversity of glyca...

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Detalles Bibliográficos
Autores principales: Jiang, Mingdi, Chattopadhyay, Aritra Nath, Li, Cheng Hsuan, Geng, Yingying, Luther, David C., Huang, Rui, Rotello, Vincent M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645398/
https://www.ncbi.nlm.nih.gov/pubmed/36519060
http://dx.doi.org/10.1039/d2sc02116a
Descripción
Sumario:Cell surface glycans serve fundamental roles in many biological processes, including cell–cell interaction, pathogen infection, and cancer metastasis. Cancer cell surface have alternative glycosylation to healthy cells, making these changes useful hallmarks of cancer. However, the diversity of glycan structures makes glycosylation profiling very challenging, with glycan ‘fingerprints’ providing an important tool for assessing cell state. In this work, we utilized the pH-responsive differential binding of boronic acid (BA) moieties with cell surface glycans to generate a high-content six-channel BA-based sensor array that uses a single polymer to distinguish mammalian cell types. This sensing platform provided efficient discrimination of cancer cells and readily discriminated between Chinese hamster ovary (CHO) glycomutants, providing evidence that discrimination is glycan-driven. The BA-functionalized polymer sensor array is readily scalable, providing access to new diagnostic and therapeutic strategies for cell surface glycosylation-associated diseases.