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Antimicrobial Agents and Chemotherapy, November 2001, p. 3175-3181, Vol. 45, No. 11
Department of Microbiology, Trinity
College,1 and School of Biotechnology,
Dublin City University,3 Dublin, Ireland, and
Center for Drug Evaluation and Research, Food and Drug
Administration, Rockville, Maryland2
Received 17 November 2000/Returned for modification 19 May
2001/Accepted 24 July 2001
The pathway of hemoglobin degradation by erythrocytic stages of the
human malarial parasite Plasmodium falciparum involves initial cleavages of globin chains, catalyzed by several endoproteases, followed by liberation of amino acids from the resulting peptides, probably by aminopeptidases. This pathway is considered a promising chemotherapeutic target, especially in view of the antimalarial synergy
observed between inhibitors of aspartyl and cysteine endoproteases. We
have applied response-surface modelling to assess antimalarial interactions between endoprotease and aminopeptidase inhibitors using
cultured P. falciparum parasites. The synergies observed were consistent with a combined role of endoproteases and
aminopeptidases in hemoglobin catabolism in this organism. As synergies
between antimicrobial agents are often inferred without proper
statistical analysis, the model used may be widely applied in studies
of antimicrobial drug interactions.
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.11.3175-3181.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Analysis of Antimalarial Synergy between Bestatin
and Endoprotease Inhibitors Using Statistical Response-Surface
Modelling
*
Corresponding author. Mailing address: Department of
Microbiology, Moyne Institute, Trinity College, Dublin 2, Ireland.
Phone: (353 1) 608 1414. Fax: (353 1) 679 9294. E-mail:
abell{at}tcd.ie.
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