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. 2018 Jun 1;293(30):11955–11965. doi: 10.1074/jbc.RA117.001369

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© 2018 by The American Society for Biochemistry and Molecular Biology, Inc.

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Figure 1. — Binding of norovirus GII.4 (Sydney, 2012, JX459908) VLPs on neoglycolipid arrays derived from high-mass human milk oligosaccharides. A, neoglycolipid fractions 1–42 correspond to HMO fractions listed in Table S1. Two micrograms of neoglycolipid were immobilized per well in a duplicate assay on polystyrene plates. B, neoglycolipids derived from standard HMOs (LNFP-I, lacto-N-fucopentaose-I; LNneoFP-I, lacto-N-neofucopentaose-I; LNFP-II, lacto-N-fucopentaose-II) and selected HMO fractions were tested in triplicate for comparative norovirus GII.4 VLP binding.