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Comparison of the Membrane Proteome of Virulent Mycobacterium tuberculosis and the Attenuated Mycobacterium bovis BCG Vaccine Strain by Label-free Quantitative Proteomics

机译:无标记定量蛋白质组学比较强毒结核分枝杆菌和牛分枝杆菌减毒分枝杆菌疫苗株的膜蛋白质组

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摘要

The Mycobacterium tuberculosis (MTB) membrane is rich in antigens that are potential targets for diagnostics and the development of new vaccines. To better understand the mechanisms underlying MTB virulence and identify new targets for therapeutic intervention we investigated the differential composition of membrane proteomes between virulent M. tuberculosis H37Rv (MTB) and the Mycobacterium bovis BCG vaccine strain. To compare the membrane proteomes, we used LC-MS/MS analysis in combination with label-free quantitative (LFQ) proteomics, utilizing the area-under-curve (AUC) of the extracted ion chromatograms (XIC) of peptides obtained from m/z and retention time alignment of MS1 features. With this approach, we obtained relative abundance ratios for 2,203 identified membrane-associated proteins in high confidence. Of these proteins, 294 showed statistically significant differences of at least 2 fold, in relative abundance between MTB and BCG membrane fractions. Our comparative analysis detected several proteins associated with known genomic regions of difference between MTB and BCG as being absent, which validated the accuracy of our approach. In further support of our label-free quantitative data, we verified select protein differences by immunoblotting. To our knowledge we have generated the first comprehensive and high coverage profile of comparative membrane proteome changes between virulent MTB and its attenuated relative BCG, which helps elucidate the proteomic basis of the intrinsic virulence of the MTB pathogen.
机译:结核分枝杆菌(MTB)膜富含抗原,这些抗原是诊断和开发新疫苗的潜在目标。为了更好地了解MTB毒力的潜在机制并确定新的治疗靶标,我们研究了结核分枝杆菌H37Rv(MTB)和牛分枝杆菌BCG疫苗株之间膜蛋白质组的差异组成。为了比较膜蛋白质组学,我们将LC-MS / MS分析与无标记定量(LFQ)蛋白质组学结合使用,利用从m /获得的肽的提取离子色谱图(XIC)的曲线下面积(AUC) z和MS1功能的保留时间对齐。通过这种方法,我们以较高的置信度获得了2203种已鉴定的膜相关蛋白的相对丰度比。在这些蛋白质中,有294个在MTB和BCG膜级分之间的相对丰度上显示出至少2倍的统计学显着性差异。我们的比较分析检测到缺少与MTB和BCG之间已知基因组差异区域相关的几种蛋白质,这验证了我们方法的准确性。为了进一步支持我们的无标签定量数据,我们通过免疫印迹验证了选择的蛋白质差异。据我们所知,我们已经产生了有毒的MTB及其减毒的相对BCG之间的比较膜蛋白质组变化的第一个全面的高覆盖图谱,这有助于阐明MTB病原体内在毒力的蛋白质组学基础。

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