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. 2014 Sep;88(18):10377–10391. doi: 10.1128/JVI.01008-14

TABLE 1.

Neoglycoconjugates used to determine the carbohydrate specificities of CNV VLPsa

Name Conjugate Structure
α-N-Acetylgalactose PAA GalNAcα1
LacNAc PAA Galβ1-4GlcNAcβ1
Forsmann disaccharide PAA GalNAcα1-3GalNAcβ1
H type 1 HSA Fucα1-2Galβ1-3GlcNAcβ1
H type 2 Both Fucα1-2Galβ1-4GlcNAcβ1
H type 3 PAA Fucα1-2Galβ1-3GalNAcα1
A heptasaccharide HSA GalNAcα1-3(Fucα1-2)Galβ1-3(Fucα1-4)GlcNAcβ1-3Galβ1-4Glcβ1
A trisaccharide Both GalNAcα1-3(Fucα1-2)Galβ1
A disaccharide PAA GalNAcα1-3Galβ1
A type 2b PAA GalNAcα1-3(Fucα1-2)Galβ1-4GlcNacβ1
Lea (Lewis a) PAA Galβ1-3(Fucα1-4)GlcNAcβ1
Leb (Lewis b) Both Fucα1-2Galβ1-3(Fucα1-4)GlcNAcβ1
Lex (Lewis x) PAA Galβ1-4(Fucα1-3)GlcNAcβ1
Ley (Lewis y) Both Fucα1-2Galβ1-4(Fucα1-3)GlcNAcβ1
3-Sulfo Lex PAA HSO3-3Galβ1-4(Fucα1-3)GlcNAcβ1
Sial Lex (sialyl-Lewis x) Both NeuAcα2-3Galβ1-4 (Fucα1-3)GlcNAcβ1
Sial Lea (sialyl-Lewis a) Both NeuAcα2-3Galβ1-4 (Fucα1-3)GlcNAcβ1
Sialyl LNF V (lacto N-fucopentose V) HSA Fucα1-2Galβ1-3(Neu5Acα2-6)GlcNAcβ1-3Galβ1-4Glc β1
Sialyl LNnT (lacto-N-neotetraose) HSA NeuAcα2-3Galβ1-4GlcNAcβ1-3Galβ1-4Glcβ1
6-Sulfo sialyl Lex PAA NeuAcα2-3Galβ1-3(Fucα1-4)(HSO3-6)GlcNAcβ1
a

Twenty-six synthetic oligosaccharides, conjugated to either PAA or HSA, were used in ELISA-based assays to investigate the ability of CNV VLPs to bind carbohydrate structures. Ten of these synthetic oligosaccharides were only available conjugated to PAA, four were only available conjugated to HSA, and a further six oligosaccharide structures were available with either PAA or HSA conjugation.