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Originally published In Press as doi:10.1074/jbc.M205152200 on June 12, 2002
J. Biol. Chem., Vol. 277, Issue 36, 32562-32570, September 6, 2002
The Expression of Free Oligosaccharides in Human Seminal
Plasma*
Sara
Chalabi ,
Richard L.
Easton ,
Manish S.
Patankar§,
Frank
A.
Lattanzio§,
Jamie C.
Morrison§,
Maria
Panico ,
Howard R.
Morris ¶,
Anne
Dell , and
Gary F.
Clark§**
From the Department of Biological Sciences, Imperial
College of Science, Technology, and Medicine,
London SW7 2AY, United Kingdom and § Department of
Physiological Sciences, Eastern Virginia Medical School,
Norfolk, Virginia 23501-1980
Human seminal plasma is a complex mixture of
proteins, glycoproteins, peptides, glycopeptides, and prostaglandins
secreted by organs of the male reproductive tract. The components of
this fluid have been implicated in the suppression of immune response, agonistic effects on sperm-egg binding, and promotion of successful implantation of the human embryo. Fractionation followed by biophysical analyses revealed that free oligosaccharides constitute a major component of the total glycoconjugates within seminal plasma. Significant findings of our analyses include the following: (i) the
concentration of free oligosaccharides is 0.3-0.4 mg/ml; (ii) mono-
and difucosylated forms of the disaccharide lactose are major
components; (iii) many of the remaining oligosaccharides are also rich
in fucose and carry Lewisx and/or Lewisy
epitopes; (iv) a subset of the oligosaccharides express the reducing end sequence (GlcNAc 1-3/4Glc) not reported in human milk
oligosaccharides; (v) oligosaccharides in seminal plasma exclusively
express type 2 (Gal 1-4GlcNAc) but not the type 1 sequences
(Gal 1-3GlcNAc) that predominate in human milk glycans; and (vi) the
structural diversity of seminal plasma oligosaccharides is far less
than human milk oligosaccharides. The agonistic effect of both fucose and fucosylated glycoconjugates on human sperm-egg binding in vitro suggests that fucosylated oligosaccharides may also promote fertilization in the female reproductive tract.
*
This work was supported by the Biotechnology and Biological
Sciences Research Council and the Wellcome Trust (to A. D. and H. R. M.), National Institutes of Health Grant HD35652 (to G. F.
C.), and Jeffress Research Grant J-584 (to M. S. P.).The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
¶
To whom correspondence may be addressed. Tel.:
44-207-225-5219; Fax: 44-207-225-0458; E-mail: h.morris@ic.ac.uk.
To whom correspondence may be addressed. Tel.:
44-207-225-5219; Fax: 44-207-225-0458; E-mail: a.dell@ic.ac.uk.
**
To whom correspondence may be addressed. Tel.: 757-446-5653; Fax:
757-624-2270; E-mail: clarkgf@evms.edu.
Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.

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Copyright © 2002 by the American Society for Biochemistry and Molecular Biology.
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