Oliveira Cláudia S, Segatto Ana L A, Nogara Pablo A, Piccoli Bruna C, Loreto Élgion L S, Aschner Michael, Rocha João B T
Programa Pós-Graduação Stricto Sensu em Biotecnologia Aplicada a Saúde da Criança e do Adolescente, Instituto de Pesquisa Pelé Pequeno Príncipe, Curitiba, Brazil.
Faculdades Pequeno Príncipe, Curitiba, Brazil.
Front Genet. 2020 May 5;11:425. doi: 10.3389/fgene.2020.00425. eCollection 2020.
Mercury is a hazardous substance that has unique neurodevelopmental toxic effects in humans. However, the precise sequence of molecular events that culminate in Hg-induced neuropathology is still unknown. Though the omics studies have been generating an enormous amount of new data about Hg toxicity, our ability to interpret such a large quantity of information is still limited. In this opinion article, we will reinforce the necessity of new high throughput and accurate analytical proteomic methodologies, especially, thiol and selenol-proteome. Overall, we posit that improvements in thiol- and selenol-proteomic analyses will be pivotal in identifying the primary cellular targets of Hg. However, a better understanding of the complex cascades and molecular pathways involved in its toxicity will require extensive complementary studies in more complex systems.
汞是一种有害物质,对人类具有独特的神经发育毒性作用。然而,最终导致汞诱导神经病理学的分子事件的确切顺序仍然未知。尽管组学研究已经产生了大量关于汞毒性的新数据,但我们解释如此大量信息的能力仍然有限。在这篇观点文章中,我们将强调新型高通量和精确分析蛋白质组学方法的必要性,特别是硫醇和硒醇蛋白质组。总体而言,我们认为硫醇和硒醇蛋白质组分析的改进对于确定汞的主要细胞靶点至关重要。然而,要更好地理解其毒性所涉及的复杂级联反应和分子途径,还需要在更复杂的系统中进行广泛的补充研究。