Post-Translational Modifications of Proteins of Malaria Parasites during the Life Cycle

被引:0
|
作者
Schwarzer, Evelin [1 ]
Skorokhod, Oleksii [2 ]
机构
[1] Univ Turin, Dept Oncol, Via Santena 5 bis, I-10126 Turin, Italy
[2] Univ Turin, Dept Life Sci & Syst Biol, Via Acad Albertina 13, I-10123 Turin, Italy
关键词
Plasmodium; mosquito Anopheles; phosphorylation; acetylation; methylation; lipidation; lipoxidation; glycosylation; ubiquitination; glutathionylation; PLASMODIUM-FALCIPARUM MALARIA; SIGNAL PEPTIDE PEPTIDASE; BLOOD-STAGE; PALMITOYL-TRANSFERASES; ANTIMALARIAL ACTIVITY; FUNCTIONAL-ANALYSIS; OXIDATIVE STRESS; IN-VITRO; CIRCUMSPOROZOITE PROTEIN; THERAPEUTIC TARGET;
D O I
10.3390/ijms25116145
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Post-translational modifications (PTMs) are essential for regulating protein functions, influencing various fundamental processes in eukaryotes. These include, but are not limited to, cell signaling, protein trafficking, the epigenetic control of gene expression, and control of the cell cycle, as well as cell proliferation, differentiation, and interactions between cells. In this review, we discuss protein PTMs that play a key role in the malaria parasite biology and its pathogenesis. Phosphorylation, acetylation, methylation, lipidation and lipoxidation, glycosylation, ubiquitination and sumoylation, nitrosylation and glutathionylation, all of which occur in malarial parasites, are reviewed. We provide information regarding the biological significance of these modifications along all phases of the complex life cycle of Plasmodium spp. Importantly, not only the parasite, but also the host and vector protein PTMs are often crucial for parasite growth and development. In addition to metabolic regulations, protein PTMs can result in epitopes that are able to elicit both innate and adaptive immune responses of the host or vector. We discuss some existing and prospective results from antimalarial drug discovery trials that target various PTM-related processes in the parasite or host.
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页数:49
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