Molecular modeling of glycosyltransferases involved in the biosynthesis of blood group A, blood group B, Forssman and iGb3 antigens and their interaction with substrates

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A novel seven membered carbohydrate phostone

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Comparative aspects of glycosyltransferases

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DMA mismatch detection by resonance energy transfer between ruthenium(II) and osmium(II) tris(2,2′-bipyridyl) chromophores

Octahedral tris-chelate complexes [M II(bpy) 3] 2+ (M = Ru or Os, bpy = 2,2′-bipyridyl), covalently attached to the 3′- and 5′phosphates of two oligonucleotides, are juxtaposed when hybridized contiguously to a fully complementary DMA target. Visible metal-to-ligand charge-transfer (MLCT) excitation of the [Ru II(bpy) 3] 2+ unit leads to resonance energy transfer to the MLCT state of the [Os II(bpy) 3] 2+ moiety, with the energy transfer efficiency depending on the degree of hybridization. The extent of attenuation of the intense red luminescence from the Ru II chromophore hence allows highly sensitive structural probing of the assembly and constitutes a novel approach to DNA sensing which is capable of detecting mutations. © 2005 American Chemical Society

Synthesis of D-galactopyranosylphosphonic and (D-galactopyranosylmethyl)phosphonic acids as intermediates of inhibitors of galactosyltransferases

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DMA mismatch detection by resonance energy transfer between ruthenium(II) and osmium(II) tris(2,2′-bipyridyl) chromophores

Octahedral tris-chelate complexes [M II(bpy) 3] 2+ (M = Ru or Os, bpy = 2,2′-bipyridyl), covalently attached to the 3′- and 5′phosphates of two oligonucleotides, are juxtaposed when hybridized contiguously to a fully complementary DMA target. Visible metal-to-ligand charge-transfer (MLCT) excitation of the [Ru II(bpy) 3] 2+ unit leads to resonance energy transfer to the MLCT state of the [Os II(bpy) 3] 2+ moiety, with the energy transfer efficiency depending on the degree of hybridization. The extent of attenuation of the intense red luminescence from the Ru II chromophore hence allows highly sensitive structural probing of the assembly and constitutes a novel approach to DNA sensing which is capable of detecting mutations. © 2005 American Chemical Society

DNA mismatch detection by resonance energy transfer between ruthenium(II) and osmium(II) tris(2,2'-bipyridyl) chromophores.

Octahedral tris-chelate complexes [M(II)(bpy)(3)](2+) (M = Ru or Os, bpy = 2,2'-bipyridyl), covalently attached to the 3'- and 5'-phosphates of two oligonucleotides, are juxtaposed when hybridized contiguously to a fully complementary DNA target. Visible metal-to-ligand charge-transfer (MLCT) excitation of the [Ru(II)(bpy)(3)](2+) unit leads to resonance energy transfer to the MLCT state of the [Os(II)(bpy)(3)](2+) moiety, with the energy transfer efficiency depending on the degree of hybridization. The extent of attenuation of the intense red luminescence from the Ru(II) chromophore hence allows highly sensitive structural probing of the assembly and constitutes a novel approach to DNA sensing which is capable of detecting mutations