Ce. Miller et al., OF 4 MURINE, ANTI-SHIGELLA DYSENTERIAE TYPE-1 O-POLYSACCHARIDE ANTIBODIES, 3 EMPLOY V-GENES THAT DIFFER EXTENSIVELY FROM THOSE OF THE 4TH, Molecular immunology, 33(16), 1996, pp. 1217-1222
Three murine, monoclonal antibodies, IgM 5286 F2, IgM 5297 C1, and IgG
5338 H4 were generated against Shigella dysenteriae type 1 O-specific
polysaccharide (O-SP)-conjugate. They are specific for the O-SP, whic
h is a poly-[alpha-L-rhamnopyranosyl-(1 --> 3)-alpha-L-rhamnopyranosyl
-(1 --> 2)-alpha(D-galactopyranosyl-(1 --> -2-deoxy-2-amino-N-acetyl-a
lpha-D-glucopyranosyl]. The VH and VL genes of these antibodies were c
loned and their sequences determined. They showed 93% homology, but we
re quite different to the primary sequence of IgM 3707 E9, of the same
O-SP-specificity, previously reported. The fine-specificities of both
IgG 5338 H4 and IgM 3707 E9 were for the same disaccharide moiety in
the O-SP, while IgMs 5286 F2 and 5297 C1 showed fine-specificity for t
he entire repeating unit of the O-SP. Therefore, divergent sequences c
an confer upon antibodies similar-, or even identical-carbohydrate-epi
tope fine-specificity. In addition, close primary sequence-homology do
es not preclude differences in antibody fine-specificity. Published by
Elsevier Science Ltd.