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Total Membrane and Immunogenic Proteomes of Macrophage- and Tick Cell-Derived Ehrlichia chaffeensis Evaluated by Liquid Chromatography-Tandem Mass Spectrometry and MALDI-TOF Methods

机译:液相色谱-串联质谱和MALDI-TOF方法评估巨噬细胞和T虫来源的恰菲埃里希氏菌的总膜和免疫原性蛋白质组

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摘要

Ehrlichia chaffeensis, a tick-transmitted rickettsial, is the causative agent of human monocytic ehrlichiosis. To examine protein expression patterns, we analyzed total, membrane, and immunogenic proteomes of E. chaffeensis originating from macrophage and tick cell cultures. Total proteins resolved by one-dimensional gel electrophoresis and subjected to liquid chromatography-electrospray ionization ion trap mass spectrometry allowed identification of 134 and 116 proteins from macrophage- and tick cell-derived E. chaffeensis, respectively. Because a majority of immunogenic proteins remained in the membrane fraction, individually picked total and immunogenic membrane proteins were also surveyed by liquid chromatography-tandem mass spectrometry and matrix-assisted laser desorption ionization-time of flight methods. The analysis aided the identification of 48 additional proteins. In all, 278 genes of the E. chaffeensis genome were verified as functional genes. They included genes for DNA and protein metabolism, energy metabolism and transport, membrane proteins, hypothetical proteins, and many novel proteins of unknown function. The data reported in this study suggest that the membrane of E. chaffeensis is very complex, having many expressed proteins. This study represents the first and the most comprehensive analysis of E. chaffeensis-expressed proteins. This also is the first study confirming the expression of nearly one-fourth of all predicted genes of the E. chaffeensis genome, validating that they are functionally active genes, and demonstrating that classic shotgun proteomic approaches are feasible for tick-transmitted intraphagosomal bacteria. The identity of novel expressed proteins reported in this study, including the large selection of membrane and immunogenic proteins, will be valuable in elucidating pathogenic mechanisms and developing effective prevention and control methods.
机译:hr传播的立克次体是恰菲埃里希氏体,是人单核细胞埃希氏菌病的病原体。为了检查蛋白质表达模式,我们分析了源自巨噬细胞和壁虱细胞培养物的恰菲大肠杆菌的总蛋白,膜蛋白和免疫原性蛋白质组。通过一维凝胶电泳分离的总蛋白质,并进行液相色谱-电喷雾电离离子阱质谱分析,可以分别鉴定出巨噬细胞和壁虱细胞衍生的恰菲菌中的134和116种蛋白质。由于大多数免疫原性蛋白质保留在膜级分中,因此还通过液相色谱-串联质谱法和基质辅助激光解吸电离-飞行时间方法对单独挑选的总免疫原性膜蛋白进行了调查。该分析有助于鉴定48种其他蛋白质。总共确认了恰菲大肠杆菌基因组的278个基因为功能基因。它们包括DNA和蛋白质代谢,能量代谢和转运的基因,膜蛋白,假设蛋白和许多功能未知的新型蛋白。这项研究报告的数据表明,恰菲埃里希氏体的膜非常复杂,具有许多表达的蛋白质。这项研究代表了恰菲埃里希体表达蛋白的首次也是最全面的分析。这也是第一个研究,证实chaffeensis大肠杆菌基因组所有预测基因的近四分之一的表达,证实它们是功能活跃的基因,并证明经典的shot弹枪蛋白质组学方法可用于tick传播的吞噬体内细菌。这项研究中报道的新型表达蛋白的身份,包括膜和免疫原性蛋白的大量选择,对于阐明致病机制和开发有效的预防和控制方法将具有重要的意义。

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