dos Santos Júnior Agenor de Castro Moreira, Kalume Dário Eluan, Camargo Ricardo, Gómez-Mendoza Diana Paola, Correa José Raimundo, Charneau Sébastien, de Sousa Marcelo Valle, de Lima Beatriz Dolabela, Ricart Carlos André Ornelas
Department of Cell Biology, Institute of Biology, University of Brasilia, Campus Darcy Ribeiro, Asa Norte, 70910-900, Brasília, Brazil.
Laboratório Interdisciplinar de Pesquisas Médicas, Instituto Oswaldo Cruz (IOC), Fundação Oswaldo Cruz (FIOCRUZ), 21040-360 Manguinhos, Rio de Janeiro, RJ, Brasil.
PLoS One. 2015 Sep 18;10(9):e0138667. doi: 10.1371/journal.pone.0138667. eCollection 2015.
Replication of Trypanosoma cruzi, the etiological agent of Chagas disease, displays peculiar features, such as absence of chromosome condensation and closed mitosis. Although previous proteome and subproteome analyses of T. cruzi have been carried out, the nuclear subproteome of this protozoan has not been described. Here, we report, for the first time to the best of our knowledge, the isolation and proteome analysis of T. cruzi nuclear fraction. For that, T. cruzi epimastigote cells were lysed and subjected to cell fractionation using two steps of sucrose density gradient centrifugation. The purity of the nuclear fraction was confirmed by phase contrast and fluorescence microscopy. Liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) allowed the identification of 864 proteins. Among those, 272 proteins were annotated as putative uncharacterized, and 275 had not been previously reported on global T. cruzi proteome analysis. Additionally, to support our enrichment method, bioinformatics analysis in DAVID was carried out. It grouped the nuclear proteins in 65 gene clusters, wherein the clusters with the highest enrichment scores harbor members with chromatin organization and DNA binding functions.
恰加斯病的病原体克氏锥虫的复制具有独特特征,如不存在染色体浓缩和封闭有丝分裂。尽管之前已对克氏锥虫进行了蛋白质组和亚蛋白质组分析,但该原生动物的核亚蛋白质组尚未被描述。在此,据我们所知,我们首次报告了克氏锥虫核组分的分离及蛋白质组分析。为此,将克氏锥虫无鞭毛体细胞裂解,并通过两步蔗糖密度梯度离心进行细胞分级分离。通过相差显微镜和荧光显微镜确认了核组分的纯度。液相色谱-串联质谱联用(LC-MS/MS)鉴定出了864种蛋白质。其中,272种蛋白质被注释为假定的未表征蛋白质,275种蛋白质在之前的克氏锥虫全蛋白质组分析中未曾报道。此外,为支持我们的富集方法,在DAVID中进行了生物信息学分析。它将核蛋白分为65个基因簇,其中富集分数最高的簇包含具有染色质组织和DNA结合功能的成员。