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Antimicrobial Agents and Chemotherapy, March 2001, p. 949-951, Vol. 45, No. 3
Department of Medicine, San Francisco General
Hospital and University of California, San Francisco, California
Received 17 July 2000/Returned for modification 2 October
2000/Accepted 15 December 2000
Falcipain-2, a cysteine protease and essential hemoglobinase of
Plasmodium falciparum, is a potential antimalarial
drug target. We compared the falcipain-2 sequences and sensitivities to
cysteine protease inhibitors of five parasite strains that differ
markedly in sensitivity to established antimalarial drugs. The sequence of falcipain-2 was highly conserved, and the sensitivities of all of
the strains to falcipain-2 inhibitors were very similar. Thus,
cross-resistance between cysteine protease inhibitors and other
antimalarial agents is not expected in parasites that are now
circulating and falcipain-2 remains a promising chemotherapeutic target.
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.3.949-951.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Comparison of Efficacies of Cysteine Protease
Inhibitors against Five Strains of Plasmodium
falciparum
*
Corresponding author. Mailing address: Department of
Medicine, Box 0811, University of California, San Francisco, CA
94143-0811. Phone: (415) 206-8845. Fax: (415) 648-8425. E-mail:
rosnthl{at}itsa.ucsf.edu.
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