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JBC, Vol. 254, Issue 24, 12531-12534, Dec, 1979
T. A. Beyer, J. I. Rearick, J. C. Paulson, J. P. Prieels, J. E. Sadler and R. L. Hill
Six purified glycosyltransferase (a beta-galactoside alpha 2 leads to 6
sialyltransferase, a beta-galactoside alpha 2 leads to 3 sialyltransferase,
an alpha-N-acetylgalactosaminide alpha 2 leads to 6 sialyltransferase, a
beta-galactoside alpha 1 leads to 2 fucosyltransferase, a
beta-N-acetylglucosaminide alpha 1 leads to 3 fucosyltransferase, and a
(fucosyl alpha 1 leads to 2) galactoside alpha 1 leads to 3
N-acetyl-galactosaminyltransferase) have been used to study the
biosynthetic pathways for formation of the nonreducing terminal
oligosaccharide sequences in mammalian glycoproteins. The two glycoproteins
used as model acceptor substrates in this study were human
asialotransferrin, which contains the nonreducing terminal oligosaccharide
sequence Gal beta 1 leads to 4GlcNAc beta 1 leads to 2Man, and antifreeze
glycoprotein, which contains oligosaccarides with the structure, Gal beta 1
leads to 3GalNAc alph 1 leads O-Thr. Sequential action of the six
glycosyltransferases on these model substrates led to the formation of
previously described oligosaccharide structures. The studies reported here
indicate that the substrate specificities of the individual enzymes dictate
the structures that can be synthesized and the pathways by which they may
be formed. The actions of a number of the transferasesare mutually
exclusive, thereby prohibiting the formation of theoretically possible
oligosaccharide structures. Oligosaccharides with the terminal sequence
NeuAc alpha 2 leads to 3(Fuc alpha 1 leads to 2)Gal beta 1 leads to 3GalNAc
and NeuAc alpha 2 leads to 6Gal beta 1 leads to 4(Fuc alpha 1 leads to
3)GlcNAc cannot be formed because the prior incorporation of sialic acid by
the sialyltransferases yields products that are not acceptor substrates for
the fucosyltransferases, and vice versa. Synthesis of other products
requires that the enzymes act sequentially in a specific order. The
structures NeuAc alpha 2 leads to 6(Fuc alpha 1 leads to 2)Gal beta 1 leads
to 4GlcNAc, Fuc alpha 1 leads to 2Gal beta 1 leads to 4(Fuc alpha 1 leads
to 3)GlcNAc, GalNAc alpha 1 leads to 3(Fuc alpha 1 leads to 2)Gal beta 1
leads to 4GlcNAc, and GalNAc alpha 1 leads to 3(Fuc alpha 1 leads to 2)Gal
beta 1 leads to 3GalNAc can only be synthesized if the fucosyl alpha 1
leads to 2 galactose linkage is formed first. Synthesis of the
pentasaccharide sequences GalNAc alpha 1 leads to 3(Fuc alpha 1 leads to
2)Gal beta 1 leads to 3(NeuAc alpha 2 leads to 6)GalNAc and GalNAc alpha 1
leads to 3(Fuc alpha 1 leads to 2)Gal beta 1 leads to 4(Fuc alpha 1 leads
to 3)GlcNAc requires that the N-acetylgalactosaminyltransferase act last on
the former structure and that the alpha 1 leads to 3 fucosyltransferase act
last on the latter. In those instances where a product can be formed by one
of two possible pathways, the comparisons of reaction rates indicate that
one pathway is usually preferred...
Biosynthesis of mammalian glycoproteins. Glycosylation pathways in the synthesis of the nonreducing terminal sequences
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