Sexton Anna E, Doerig Christian, Creek Darren J, Carvalho Teresa G
Drug Delivery Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences , Monash University , 381 Royal Parade , Parkville , VIC 3052 , Australia.
Centre for Chronic, Inflammatory and Infectious Diseases, Biomedical Sciences Cluster, School of Health and Biomedical Sciences , RMIT University , 264 Plenty Road , Bundoora , VIC 3083 , Australia.
ACS Infect Dis. 2019 Aug 9;5(8):1269-1278. doi: 10.1021/acsinfecdis.9b00093. Epub 2019 Jun 20.
are evolutionarily distant from model eukaryotes, and as a consequence they exhibit many non-canonical cellular processes. In the post-genomic era, functional "omics" disciplines (transcriptomics, proteomics, and metabolomics) have accelerated our understanding of unique aspects of the biology of malaria parasites. Functional "omics" tools, in combination with genetic manipulations, have offered new opportunities to investigate the function of previously uncharacterized genes. Knowledge of basic parasite biology is fundamental to understanding drug modes of action, mechanisms of drug resistance, and relevance of vaccine candidates. This Perspective highlights recent "omics"-based discoveries in basic biology and gene function of the most virulent human malaria parasite, .
它们在进化上与模式真核生物距离较远,因此表现出许多非经典的细胞过程。在后基因组时代,功能性“组学”学科(转录组学、蛋白质组学和代谢组学)加速了我们对疟原虫生物学独特方面的理解。功能性“组学”工具与基因操作相结合,为研究以前未表征基因的功能提供了新机会。了解寄生虫的基础生物学对于理解药物作用模式、耐药机制以及疫苗候选物的相关性至关重要。本综述强调了基于“组学”的关于最具毒性的人类疟原虫基础生物学和基因功能的最新发现。