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Volume 272, Number 10,
Issue of March 7, 1997
pp. 6428-6439
©1997 by The American Society for Biochemistry and Molecular Biology, Inc.
Glycosylphosphatidylinositol Anchors Represent the Major
Carbohydrate Modification in Proteins of Intraerythrocytic Stage
Plasmodium falciparum
(Received for publication, May 17, 1996, and in revised form, October 24, 1996)
D. Channe
Gowda
,
Priyadarshan
Gupta
and
Eugene A.
Davidson
From the Department of Biochemistry and Molecular Biology,
Georgetown University Medical Center, Washington, D. C. 20007
The nature and extent of carbohydrate
modification in intraerythrocytic stage Plasmodium
falciparum proteins have been controversial. This study describes
the characterization of the carbohydrates in intraerythrocytic P. falciparum proteins and provides an overall picture of the nature
of carbohydrate modification in the parasite proteins. P. falciparum strains were metabolically labeled with radioactive
sugar precursors and ethanolamine at different developmental stages.
The individual parasite proteins separated on SDS-polyacrylamide gels
and whole parasite cell lysates were analyzed for the carbohydrate moieties. The results established the following: 1)
glycosylphosphatidylinositol (GPI) anchors represent the major
carbohydrate modification in the intraerythrocytic stage P. falciparum proteins; 2) in contrast to previous reports,
O-linked carbohydrates are either absent or present only at
very low levels in the parasite; and 3) P. falciparum
contains low levels of N-glycosylation capability. The
amount of N-linked carbohydrates in whole parasite proteins is ~6% compared with the GPI anchors attached to proteins based on
radioactive GlcN incorporated into the proteins.
The glycan cores of multiple parasite protein GPI anchors are all
similar, consisting of
protein-ethanolamine-phosphate-(Man 1-2)6Man 1-2Man 1-6Man 1- 4GlcN.
The fourth Man residues distal to GlcN of the GPI anchor glycan
cores contain unidentified substituents that are susceptible to
conditions of nitrous acid deamination. This unusual structural feature
may contribute to the reported pathogenic properties of the P. falciparum GPI anchors.

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Copyright © 1997 by the American Society for Biochemistry and Molecular Biology.
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