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PMID: 10932227 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Import of host delta-aminolevulinate dehydratase into the malarial parasite: identification of a new drug target.

Nature medicine ·Vol. 6 ·No. 8 ·2000-08-00 ·Pages 898-903

Bonday ZQ, Dhanasekaran S, Rangarajan PN, Padmanaban G

Abstract

The parasite Plasmodium berghei imports the enzyme delta-aminolevulinate dehydratase (ALAD), and perhaps the subsequent enzymes of the pathway from the host red blood cell to sustain heme synthesis. Here we have studied the mechanism of this import. A 65-kDa protein on the P. berghei membrane specifically bound to mouse red blood cell ALAD, and a 93-amino-acid fragment (ALAD-DeltaNC) of the host erythrocyte ALAD was able to compete with the full-length enzyme for binding to the P. berghei membrane. ALAD-DeltaNC was taken up by the infected red blood cell when added to a culture of P. falciparum and this led to a substantial decrease in ALAD protein and enzyme activity and, subsequently, heme synthesis in the parasite, resulting in its death.

MeSH Terms
Animals Antimalarials/pharmacology Biological Transport, Active Cell Membrane/enzymology Erythrocytes/enzymology,parasitology Heme/biosynthesis Malaria/drug therapy,enzymology,parasitology Mice Mice, Inbred BALB C Plasmodium berghei/drug effects,enzymology Porphobilinogen Synthase/genetics,metabolism
Chemicals
Antimalarials Heme Porphobilinogen Synthase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Bonday Z Q
Department of Biochemistry, Indian Institute of Science Bangalore: 560 012, India.
Dhanasekaran S
Rangarajan P N
Padmanaban G
Article Info
Journal
Nature medicine
Abbr.
Nat Med
ISSN
1078-8956
Published
2000-08-00
Pages
898-903
Language
English
Region
United States
NLM ID
9502015
Subset
IM
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