Novel Ion Channel Genes in Malaria Parasites

被引:1
作者
Desai, Sanjay A. [1 ]
机构
[1] Natl Inst Allergy & Infect Dis, Lab Malaria & Vector Res, NIH, Rockville, MD 20852 USA
基金
美国国家卫生研究院;
关键词
ion channels; nutrient uptake; protein export; transmembrane transport; malaria; Plasmodium falciparum; antimalarial therapies; SURFACE ANION CHANNEL; PARASITOPHOROUS VACUOLE MEMBRANE; PLASMODIUM-FALCIPARUM MALARIA; RED-BLOOD-CELLS; INFECTED ERYTHROCYTES; PROTEIN EXPORT; PERMEABILITY PATHWAYS; CALCIUM-TRANSPORT; DRUG-RESISTANCE; RHOPTRY PROTEIN;
D O I
10.3390/genes15030296
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Ion channels serve many cellular functions including ion homeostasis, volume regulation, signaling, nutrient acquisition, and developmental progression. Although the complex life cycles of malaria parasites necessitate ion and solute flux across membranes, the whole-genome sequencing of the human pathogen Plasmodium falciparum revealed remarkably few orthologs of known ion channel genes. Contrasting with this, biochemical studies have implicated the channel-mediated flux of ions and nutritive solutes across several membranes in infected erythrocytes. Here, I review advances in the cellular and molecular biology of ion channels in malaria parasites. These studies have implicated novel parasite genes in the formation of at least two ion channels, with additional ion channels likely present in various membranes and parasite stages. Computational approaches that rely on homology to known channel genes from higher organisms will not be very helpful in identifying the molecular determinants of these activities. Given their unusual properties, novel molecular and structural features, and essential roles in pathogen survival and development, parasite channels should be promising targets for therapy development.
引用
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页数:18
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