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Protecting-Group-Free Synthesis of Glycopolymers and Their Binding Assay with Lectin and Influenza Virus

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Part of the book series: Methods in Molecular Biology ((MIMB,volume 1367))

Abstract

Typical synthetic methods for glycopolymers are laborious and require multistep processes, including protection and deprotection steps. Here we describe a facile protecting-group-free synthetic approach to glycopolymers bearing oligosaccharides from free saccharides by direct azidation and click chemistry methods, followed by reversible addition-fragmentation chain transfer polymerization. This method can be applied not only to mono- and disaccharides, but also to large biologically relevant oligosaccharides having sialic acids. Due to the glycocluster effect, the glycopolymers strongly bind with the corresponding lectin and influenza A virus, as analyzed by the quartz crystal microbalance method and hemagglutination inhibition assay.

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Acknowledgment

This work was financially supported by JSPS KAKENHI Grant No. 25810075.

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Correspondence to Tomonari Tanaka .

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Tanaka, T., Takahashi, T., Suzuki, T. (2016). Protecting-Group-Free Synthesis of Glycopolymers and Their Binding Assay with Lectin and Influenza Virus. In: Sun, XL. (eds) Macro-Glycoligands. Methods in Molecular Biology, vol 1367. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-3130-9_4

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  • DOI: https://doi.org/10.1007/978-1-4939-3130-9_4

  • Publisher Name: Humana Press, New York, NY

  • Print ISBN: 978-1-4939-3129-3

  • Online ISBN: 978-1-4939-3130-9

  • eBook Packages: Springer Protocols

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