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  Fucose-functionalized precision glycomacromolecules targeting human norovirus capsid protein

Bücher, K. S., Yan, H., Creutznacher, R., Ruoff, K., Mallagaray, A., Grafmüller, A., et al. (2018). Fucose-functionalized precision glycomacromolecules targeting human norovirus capsid protein. Macromolecules, 19(9), 3714-3724. doi:10.1021/acs.biomac.8b00829.

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Item Permalink: https://hdl.handle.net/21.11116/0000-0001-ED99-8 Version Permalink: https://hdl.handle.net/21.11116/0000-0002-52FD-5
Genre: Journal Article

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Bücher, Katharina Susanne, Author
Yan, Hao, Author
Creutznacher, Robert, Author
Ruoff, Kerstin, Author
Mallagaray, Alvaro, Author
Grafmüller, Andrea1, Author           
Dirks, Jan Sebastian, Author
Kilic, Turgay, Author
Weickert, Sabrina, Author
Rubailo, Anna, Author
Drescher, Malte, Author
Schmidt, Stephan, Author
Hansman, Grant, Author
Peters, Thomas, Author
Uetrecht, Charlotte, Author
Hartmann, Laura, Author
Affiliations:
1Andrea Grafmüller, Theorie & Bio-Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863323              

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 Abstract: Norovirus infection is the major cause of non-bacterial gastroenteritis in humans and has been the subject of numerous studies investigating the virus’s biophysical properties and biochemical function with the aim of deriving novel and highly potent entry inhibitors to prevent infection. Recently, it has been shown that the protruding P domain dimer (P-dimer) of a GII.10 Norovirus strain exhibits two new binding sites for L-fucose in addition to the canonical binding sites. Thus these sites provide a novel target for the design of multivalent fucose ligands as entry inhibitors of norovirus infections. In this current study, a first generation of multivalent fucose-functionalized glycomacromolecules was synthesized and applied as model structures to investigate the potential targeting of fucose binding sites in human norovirus P-dimer. Following previously established solid phase polymer synthesis, eight precision glycomacromolecules varying in number and position of fucose ligands along an oligo(amidoamine) backbone were obtained and then used in a series of binding studies applying native MS, NMR and X-ray crystallography. We observed only one fucose per glycomacromolecule binding to one P-dimer resulting in similar binding affinities for all fucose-functionalized glycomacromolecules, which based on our current findings we attribute to the overall size of macromolecular ligands and possibly to steric hindrance.

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 Dates: 2018-08-022018-09-10
 Publication Status: Issued
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 Rev. Type: Peer
 Identifiers: DOI: 10.1021/acs.biomac.8b00829
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Title: Macromolecules
Source Genre: Journal
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Publ. Info: Washington, D.C. : American Chemical Society
Pages: - Volume / Issue: 19 (9) Sequence Number: - Start / End Page: 3714 - 3724 Identifier: ISSN: 0024-9297