Research

Characterization of two putative potassium channels in Plasmodium falciparum

Karena L Waller^1,5 , Sean M McBride² , Kami Kim^3,4 and Thomas V McDonald^1,2

¹Department of Medicine (Cardiology), Albert Einstein College of Medicine, 1300 Morris Park Ave., Bronx NY 10461, USA

²Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx NY 10461, USA

³Department of Medicine (Infectious Diseases), Albert Einstein College of Medicine, Bronx NY 10461, USA

⁴Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx NY 10461, USA

⁵Department of Microbiology, Monash University, Clayton VIC 3800, Australia

author email corresponding author email

Malaria Journal 2008, 7:19doi:10.1186/1475-2875-7-19

Published:	24 January 2008

Abstract

Background

Potassium channels are essential for cell survival and participate in the regulation of cell membrane potential and electrochemical gradients. During its lifecycle, Plasmodium falciparum parasites must successfully traverse widely diverse environmental milieus, in which K⁺ channel function is likely to be critical. Dramatically differing conditions will be presented to the parasite in the mosquito mid-gut, red blood cell (RBC) cytosol and the human circulatory system.

Methods

In silico sequence analyses identified two open-reading frames in the P. falciparum genome that are predicted to encode for proteins with high homology to K⁺ channels. To further analyse these putative channels, specific antisera were generated and used in immunoblot and immunofluorescence analyses of P. falciparum-infected RBCs. Recombinant genome methods in cultured P. falciparum were used to create genetic knock outs of each K⁺ channel gene to asses the importance of their expression.

Results

Immunoblot and IFA analyses confirmed the expression of the two putative P. falciparum K⁺ channels (PfK1 and PfK2). PfK1 is expressed in all asexual stage parasites, predominantly in late stages and localizes to the RBC membrane. Conversely, PfK2 is predominantly expressed in late schizont and merozoite stage parasites and remains primarily localized to the parasite. Repeated attempts to knockout PfK1 and PfK2 expression by targeted gene disruption proved unsuccessful despite evidence of recombinant gene integration, indicating that pfk1 and pfk2 are apparently refractory to genetic disruption.

Conclusion

Putative K⁺ channel proteins PfK1 and PfK2 are expressed in cultured P. falciparum parasites with differing spatial and temporal patterns. Eventual functional characterization of these channels may reveal future pharmacological targets.