Mitsakos A, Hanisch F G, Uhlenbruck G
Institut für Immunbiologie, Medizinische Universitätsklinik Köln.
Biol Chem Hoppe Seyler. 1988 Aug;369(8):661-5. doi: 10.1515/bchm3.1988.369.2.661.
Biosynthesis of the sialyl-Lex determinant (NeuAc alpha 2-3Gal beta 1-4(Fuc alpha 1-3)-GlcNAc beta 1-3-R) in human amniotic fluid has been shown to proceed via the same sequence of glycosylation steps established previously for lung carcinoma PC 9 cells (Holmes, E. H., Ostrander, G.K. & Hakomori, S. (1986) J. Biol. Chem. 261, 3737-3743): sialylation of type-2-chain-precursor substrates (paragloboside) by an amniotic alpha 2-3-sialyltransferase precedes fucosylation of sialylated intermediates (sialosyl paragloboside) by an organ-characteristic alpha 1-3-L-fucosyltransferase.
人羊水唾液酸化-Lex决定簇(NeuAcα2-3Galβ1-4(Fucα1-3)-GlcNAcβ1-3-R)的生物合成已被证明是通过先前为肺癌PC 9细胞确定的相同糖基化步骤序列进行的(霍姆斯,E.H.,奥斯特兰德,G.K.和哈科莫里,S.(1986年)《生物化学杂志》261卷,3737-3743页):2型链前体底物(副球蛋白)由羊水α2-3-唾液酸转移酶进行唾液酸化,然后由器官特异性α1-3-L-岩藻糖转移酶对唾液酸化中间体(唾液酸副球蛋白)进行岩藻糖基化。