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Volume 270,
Number 27,
Issue of July 07, pp. 16327-16332, 1995
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
Purification
and Characterization of the GalNAc-4-sulfotransferase Responsible for
Sulfation of GalNAc 1,4GlcNAc-bearing Oligosaccharides
Lora V.
Hooper
,
Ole
Hindsgaul
,
Jacques
U.
Baenziger
The pituitary glycoprotein hormone lutropin is characterized by
its pulsatile appearance in the bloodstream which is important for the
expression of its biological activity in the ovary. We have previously
shown that lutropin bears unique Asn-linked oligosaccharides
terminating with GalNAc-4-SO which allow the hormone to be
rapidly cleared from the bloodstream via a specific receptor in the
liver, thus contributing to its pulsatile appearance in the
circulation. Furthermore, we have found that carbonic anhydrase VI,
synthesized by the submaxillary gland and secreted into the saliva,
also bears Asn-linked oligosaccharides terminating with
GalNAc-4-SO , suggesting that this unique sulfated structure
mediates other biological functions in addition to rapid clearance from
the circulation. We report here the purification of a
GalNAc-4-sulfotransferase which transfers sulfate to terminal
1,4-linked GalNAc on Asn-linked oligosaccharides. We show that the
purified submaxillary gland enzyme has kinetic parameters identical to
the pituitary enzyme, indicating that the same sulfotransferase is
responsible for the sulfation of lutropin oligosaccharides in pituitary
and carbonic anhydrase VI oligosaccharides in submaxillary gland. This
GalNAc-4-sulfotransferase has an apparent molecular mass of 128 kDa and
can be specifically photoaffinity radiolabeled with 3`,5`-ADP, a
competitive inhibitor of sulfotransferase activity. The acceptor
specificity of this GalNAc-4-sulfotransferase indicates that it is able
to transfer sulfate to terminal GalNAc 1,4GlcNAc on both N- and O-glycosidically linked oligosaccharides,
suggesting that this enzyme is also responsible for the sulfation of O-linked glycans on proopiomelanocortin.

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Copyright © 1995 by the American Society for Biochemistry and Molecular Biology.
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