Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.tmaid.2006.01.015
Title: Plasmodium falciparum pyruvate kinase as a novel target for antimalarial drug-screening
Authors: Chan, M. 
Tan, D.S.H. 
Sim, T.S. 
Keywords: cDNA
Glycolysis
Malaria
Plasmodium falciparum
Pyruvate kinase
Issue Date: 2007
Source: Chan, M.,Tan, D.S.H.,Sim, T.S. (2007). Plasmodium falciparum pyruvate kinase as a novel target for antimalarial drug-screening. Travel Medicine and Infectious Disease 5 (2 SPEC. ISS.) : 125-131. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tmaid.2006.01.015
Abstract: Background: Global travellers are increasingly at risk of contracting malaria. The increasing occurrence of drug-resistance in many endemic areas emphasizes the need for novel drug targets for antimalarial-screening. In this study, the use of pyruvate kinase as a drug-target is evaluated. The functional validation of a gene encoding pyruvate kinase (designated PK1) has previously been reported. However, alternative copies of this enzyme encoded by Plasmodium falciparum could also circumvent the role of PK1. A survey of genome data revealed a putative ORF seemingly coding for another pyruvate kinase (designated PK2). Methods: The expression of PK1 and PK2 in in vitro cultures were investigated by RT-PCR. Biocomputational analysis was carried out to identify structural differences between the P. falciparum pyruvate kinases and the corresponding enzymes from its human host. Results: Both PK1 and PK2 were indeed actively transcribed during the intraerythrocytic stages, suggesting the involvement of both enzymes during infection. A comparison of amino acid residues at the effector binding sites of PK1 and PK2, to those of the human pyruvate kinases revealed some significant differences that could serve as targets for selective inhibitors to be designed against parasitic pyruvate kinases. Conclusion: Experimental evidence for the expression of both PK1 and PK2 during the blood stages of malaria infection was provided. Interestingly, phylogenetic analysis revealed that the "PK2" type of enzyme appears to be confined to Apicomplexans, an important observation with respect to the assessment of PK2 as a drug-target. © 2006 Elsevier Ltd. All rights reserved.
Source Title: Travel Medicine and Infectious Disease
URI: http://scholarbank.nus.edu.sg/handle/10635/24655
ISSN: 14778939
DOI: 10.1016/j.tmaid.2006.01.015
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

SCOPUSTM   
Citations

15
checked on Dec 12, 2017

Page view(s)

147
checked on Dec 15, 2017

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.