CSIR-Centre for Cellular and Molecular Biology, Habsiguda, Uppal Road, Hyderabad, 500007, TS, India.
Academy of Scientific and Innovative Research, Ghaziabad, 201002, UP, India.
Sci Rep. 2020 Nov 19;10(1):20220. doi: 10.1038/s41598-020-77001-5.
A variety of post-translational modifications of Plasmodium falciparum proteins, including phosphorylation and ubiquitination, are shown to have key regulatory roles during parasite development. NEDD8 is a ubiquitin-like modifier of cullin-RING E3 ubiquitin ligases, which regulates diverse cellular processes. Although neddylation is conserved in eukaryotes, it is yet to be characterized in Plasmodium and related apicomplexan parasites. We characterized P. falciparum NEDD8 (PfNEDD8) and identified cullins as its physiological substrates. PfNEDD8 is a 76 amino acid residue protein without the C-terminal tail, indicating that it can be readily conjugated. The wild type and mutant (Gly75Ala/Gly76Ala) PfNEDD8 were expressed in P. falciparum. Western blot of wild type PfNEDD8-expressing parasites indicated multiple high molecular weight conjugates, which were absent in the parasites expressing the mutant, indicating conjugation of NEDD8 through Gly76. Immunoprecipitation followed by mass spectrometry of wild type PfNEDD8-expressing parasites identified two putative cullins. Furthermore, we expressed PfNEDD8 in mutant S. cerevisiae strains that lacked endogenous NEDD8 (rub1Δ) or NEDD8 conjugating E2 enzyme (ubc12Δ). The PfNEDD8 immunoprecipitate also contained S. cerevisiae cullin cdc53, further substantiating cullins as physiological substrates of PfNEDD8. Our findings lay ground for investigation of specific roles and drug target potential of neddylation in malaria parasites.
疟原虫蛋白的各种翻译后修饰,包括磷酸化和泛素化,被证明在寄生虫发育过程中具有关键的调节作用。NEDD8 是一种泛素样修饰物,可调节 cullin-RING E3 泛素连接酶,从而调节多种细胞过程。尽管 neddylation 在真核生物中是保守的,但它在疟原虫和相关的顶复门寄生虫中尚未被描述。我们对疟原虫 NEDD8(PfNEDD8)进行了特征描述,并鉴定了 cullins 作为其生理底物。PfNEDD8 是一种 76 个氨基酸残基的蛋白质,没有 C 末端尾部,这表明它可以很容易地被共轭。野生型和突变型(Gly75Ala/Gly76Ala)PfNEDD8 在疟原虫中表达。野生型 PfNEDD8 表达寄生虫的 Western blot 显示出多个高分子量的缀合物,而在表达突变型的寄生虫中则不存在,这表明 NEDD8 通过 Gly76 进行缀合。对野生型 PfNEDD8 表达寄生虫进行免疫沉淀和质谱分析,鉴定出两种可能的 cullins。此外,我们在缺乏内源性 NEDD8(rub1Δ)或 NEDD8 缀合 E2 酶(ubc12Δ)的突变型 S. cerevisiae 菌株中表达 PfNEDD8。PfNEDD8 的免疫沉淀也含有 S. cerevisiae cullin cdc53,进一步证实 cullins 是 PfNEDD8 的生理底物。我们的发现为研究 neddylation 在疟原虫中的特定作用和药物靶标潜力奠定了基础。