Baisch G, Ohrlein R, Streiff M, Kolbinger F
Novartis Pharma AG, Schwarzwaldallee, Basle, Switzerland.
Bioorg Med Chem Lett. 1998 Apr 7;8(7):755-8. doi: 10.1016/s0960-894x(98)00092-4.
A series of sialylated type-I sugars, which have the natural N-acetyl group of the glucosamine moiety replaced by a wide range of amides, is incubated with recombinant fucosyl-transferase III and non-natural guanosine-diphosphate activated donor-sugars. Surprisingly, the enzyme tolerates the simultaneous alterations on the donor and acceptor to form a wide array of sialyl-Lewis(a)-analogues.
一系列唾液酸化的I型糖,其葡糖胺部分的天然N-乙酰基被多种酰胺取代,与重组岩藻糖基转移酶III和非天然鸟苷二磷酸活化的供体糖一起孵育。令人惊讶的是,该酶能够耐受供体和受体上的同时改变,从而形成多种唾液酸化路易斯(a)类似物。