Plasmodium falciparum M1-Aminopeptidase: A Promising Target for the Development of Antimalarials

Author(s): Jorge Gonzalez-Bacerio , Rafael Fando , Alberto del Monte-Martinez , Jean-Louis Charli , Maria de los A. Chávez .

Journal Name: Current Drug Targets

Volume 15 , Issue 12 , 2014

  Journal Home
Translate in Chinese
Become EABM
Become Reviewer

Abstract:

Malaria is a devastating human parasitic disease that receives enhanced attention due to the emergence of resistance to traditional drugs. Thus, the search for new molecular targets is a major goal. PfAM1 is an aminopeptidase from Plasmodium falciparum, William H. Welch 1897, belonging to the M1 family of metalloproteases, which is a promising target of inhibitors to block the intra-erythrocytic stages of the parasite. Since its identification in 1998, many efforts have been done to validate PfAM1 as an appropriate target of antimalarials. The present work is a critical review of the main structural, functional and kinetic characteristics of PfAM1, as well as a summary of the effects of key inhibitors at molecular and cellular levels. The systematization of experimental results should contribute to a better understanding of the properties of PfAM1 as a target of antimalarials and promote research projects focused on the development of PfAM1 inhibitors.

Keywords: Antimalarials, growth inhibition, M1 family, metallo-aminopeptidases, Plasmodium falciparum, protease inhibitors.

Rights & PermissionsPrintExport Cite as

Article Details

VOLUME: 15
ISSUE: 12
Year: 2014
Page: [1144 - 1165]
Pages: 22
DOI: 10.2174/1389450115666141024115641
Price: $58

Article Metrics

PDF: 22