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• W2555264230 abstract "The interactions between soluble carbohydrates and/or surface displayed glycans and protein receptors are essential to many biological processes and cellular recognition events. Carbohydrate microarrays provide opportunities for high-throughput quantitative analysis of carbohydrate-protein interactions. Over the past decade, various techniques have been implemented for immobilizing glycans on solid surfaces in a microarray format. Herein, we describe a detailed protocol for fabricating carbohydrate microarrays that capitalizes on the intrinsic reactivity of boronic acid toward carbohydrates to form stable boronate diesters. A large variety of unprotected carbohydrates ranging in structure from simple disaccharides and trisaccharides to considerably more complex human milk and blood group (oligo)saccharides have been covalently immobilized in a single step on glass slides, which were derivatized with high-affinity boronic acid ligands. The immobilized ligands in these microarrays maintain the receptor-binding activities including those of lectins and antibodies according to the structures of their pendant carbohydrates for rapid analysis of a number of carbohydrate-recognition events within 30 h. This method facilitates the direct construction of otherwise difficult to obtain carbohydrate microarrays from underivatized glycans." @default.
• W2555264230 created "2016-11-30" @default.
• W2555264230 creator A5008211573 @default.
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• W2555264230 date "2016-11-22" @default.
• W2555264230 modified "2023-09-22" @default.
• W2555264230 title "Fabrication of Carbohydrate Microarrays by Boronate Formation" @default.
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• W2555264230 doi "https://doi.org/10.1007/978-1-4939-6584-7_4" @default.
• W2555264230 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27873199" @default.
• W2555264230 hasPublicationYear "2016" @default.
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