Department of Veterinary Biosciences, Melbourne Veterinary School, The University of Melbourne, Parkville, Victoria 3010, Australia.
Bio21 Mass Spectrometry and Proteomics Facility, The University of Melbourne, Parkville, Victoria 3010, Australia.
J Proteomics. 2020 Feb 20;213:103615. doi: 10.1016/j.jprot.2019.103615. Epub 2019 Dec 14.
Protein phosphorylation plays essential roles in many cellular processes. Despite recent progress in the genomics, transcriptomics and proteomics of socioeconomically important parasitic nematodes, there is scant phosphoproteomic data to underpin molecular biological discovery. Here, using the phosphopeptide enrichment-based LC-MS/MS and data-independent acquisition (DIA) quantitation, we characterised the first developmental phosphoproteome of the parasitic nematode Haemonchus contortus - one of the most pathogenic parasites of ruminant livestock. Totally, 1804 phosphorylated proteins with 4406 phosphorylation sites ('phosphosites') from different developmental stages/sexes were identified. Bioinformatic analyses of quantified 'phosphosites' exhibited distinctive stage- and sex-specific patterns during development, and identified a subset of phosphoproteins proposed to play crucial roles in processes such as spindle positioning, signal transduction and kinase activity. A sequence-based comparison of the phosphoproteome of H. contortus with those of two free-living nematode species (Caenorhabditis elegans and Pristionchus pacificus) suggested a limited number of common protein phosphorylation events among these species. Our findings infer active roles for protein phosphorylation in the adaptation of a parasitic nematode to a constantly changing external environment. The phosphoproteomic data set for H. contortus provides a basis to better understand phosphorylation and associated biological processes (e.g., regulation of signal transduction), and might enable the discovery of novel anthelmintic targets. SIGNIFICANCE: Here, we report the first phosphoproteome for a socioeconomically parasitic nematode (Haemonchus contortus). This phosphoproteome exhibits distinctive patterns during development, suggesting active roles of post-translational modification in the parasite's adaptation to changing environments within and outside of the host animal. This work sheds a light on the developmental phosphorylation in a parasitic nematode, and could enable the discovery of novel interventions against major pathogens.
蛋白质磷酸化在许多细胞过程中起着至关重要的作用。尽管在具有社会经济重要性的寄生线虫的基因组学、转录组学和蛋白质组学方面取得了最近的进展,但几乎没有磷酸蛋白质组学数据来支持分子生物学发现。在这里,我们使用基于磷酸肽富集的 LC-MS/MS 和无信息获取 (DIA) 定量方法,描述了寄生线虫旋毛虫的第一个发育磷酸蛋白质组——反刍动物牲畜中最具致病性的寄生虫之一。总共从不同发育阶段/性别中鉴定出 1804 种具有 4406 个磷酸化位点(“磷酸化位点”)的磷酸化蛋白。对定量“磷酸化位点”的生物信息学分析表明,在发育过程中存在明显的阶段和性别特异性模式,并鉴定出一组磷酸蛋白,这些蛋白被认为在纺锤体定位、信号转导和激酶活性等过程中发挥关键作用。旋毛虫的磷酸蛋白质组与两种自由生活线虫物种(秀丽隐杆线虫和太平洋真涡虫)的磷酸蛋白质组的序列比较表明,这些物种之间共同的蛋白质磷酸化事件数量有限。我们的研究结果推断,蛋白质磷酸化在寄生线虫适应不断变化的外部环境中发挥着积极的作用。旋毛虫的磷酸蛋白质组数据集为更好地理解磷酸化和相关生物学过程(例如,信号转导的调节)提供了基础,并可能发现新的驱虫靶点。意义:在这里,我们报告了第一个具有社会经济重要性的寄生线虫(旋毛虫)的磷酸蛋白质组。该磷酸蛋白质组在发育过程中表现出独特的模式,表明翻译后修饰在寄生虫适应宿主内外环境变化中的积极作用。这项工作揭示了寄生线虫发育中的磷酸化作用,并可能发现针对主要病原体的新干预措施。