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J Biol Chem, Vol. 273, Issue 7, 3884-3887, February 13, 1998
From the New York University Medical Center, Department of
Pathology, New York, New York 10016
Haptoglobin-related protein (HPR) is a serum
protein that is >90% homologous to the acute-phase reactant
haptoglobin (Hp). Haptoglobin binds and removes free hemoglobin (Hb)
from the circulation. Hpr levels are elevated with tumor progression in
the serum of some cancer patients, but the relevance of this
observation is not understood. HPR is an integral part of two distinct
high molecular weight complexes (trypanosome lytic factor 1 (TLF1) and
TLF2) that are lytic for the African parasite Trypanosoma brucei
brucei. Previous data indicate that HPR represents the toxic
component of both trypanosome lytic factors. It has been proposed that
after uptake by the parasite, Hb bound to HPR causes lysis in a
peroxidase-dependent process. We report that the molecular
architecture of HPR in normal human serum is different from that of Hp
and that HPR does not bind Hb in normal human serum. Immunodepletion of
all detectable Hb from TLF1 does not deplete TLF1 of HPR or
trypanolytic activity, suggesting that the mechanism of parasite lysis
is Hb-independent.
Characterization of the Human Serum Trypanosome Toxin,
Haptoglobin-related Protein
Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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