Srivastava G, Hindsgaul O
Department of Chemistry, University of Alberta, Edmonton, Canada.
Carbohydr Res. 1992 Feb 7;224:83-93. doi: 10.1016/0008-6215(92)84095-a.
The tetrasaccharide beta-D-Galp-(1----4)-beta-D-GlcpNAc-(1----6)-alpha-D- Manp-(1----6)-beta-D-Manp-OR (2) and the pentasaccharide beta-D-GlcpNAc-(1----3)-beta-D-Galp-(1----4)-beta-D- GlcpNAc-(1----6)-alpha-D-Manp-(1----6)-beta-D-Manp-OR (3), where R = (CH2)8COOMe, have been prepared by using combined chemical and enzymic procedures. Structure 2 is a substrate for UDP-GlcpNAc:beta-D-Galp-(1----4)- beta-D-GlcpNAc (GlcNAc to Gal) beta(1----3)-N-acetylglucosaminyltransferase, and 3 would be the product of its action. Antibodies raised against 3 are intended for use in an ELISA assay that would quantitate the enzymic conversion of immobilized 2 into 3.
四糖β-D-半乳糖基-(1→4)-β-D-氨基葡萄糖基-(1→6)-α-D-甘露糖基-(1→6)-β-D-甘露糖-OR(2)和五糖β-D-氨基葡萄糖基-(1→3)-β-D-半乳糖基-(1→4)-β-D-氨基葡萄糖基-(1→6)-α-D-甘露糖基-(1→6)-β-D-甘露糖-OR(3),其中R =(CH2)8COOMe,已通过化学和酶促联合方法制备。结构2是UDP-氨基葡萄糖:β-D-半乳糖基-(1→4)-β-D-氨基葡萄糖(氨基葡萄糖到半乳糖)β(1→3)-N-乙酰氨基葡萄糖转移酶的底物,3将是其作用产物。针对3产生的抗体用于ELISA测定,该测定将定量固定化的2酶促转化为3的过程。