| Literature DB >> 33517144 |
Jianhua Wang1, Ning Jiang2, Xiaoyu Sang2, Na Yang2, Ying Feng2, Ran Chen2, Xinyi Wang3, Qijun Chen4.
Abstract
Malaria elimination is still pending on the development of novel tools that rely on a deep understanding of parasite biology. Proteins of all living cells undergo myriad posttranslational modifications (PTMs) that are critical to multifarious life processes. An extensive proteome-wide dissection revealed a fine PTM map of most proteins in both Plasmodium falciparum, the causative agent of severe malaria, and the infected red blood cells. More than two-thirds of proteins of the parasite and its host cell underwent extensive and dynamic modification throughout the erythrocytic developmental stage. PTMs critically modulate the virulence factors involved in the host-parasite interaction and pathogenesis. Furthermore, P. falciparum stabilized the supporting proteins of erythrocyte origin by selective demodification. Collectively, our multiple omic analyses, apart from having furthered a deep understanding of the systems biology of P. falciparum and malaria pathogenesis, provide a valuable resource for mining new antimalarial targets.Entities:
Keywords: Plasmodium falciparum; molecular function; protein posttranslational modification; regulation
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Year: 2020 PMID: 33517144 PMCID: PMC7857547 DOI: 10.1074/mcp.RA120.002375
Source DB: PubMed Journal: Mol Cell Proteomics ISSN: 1535-9476 Impact factor: 5.911