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Gel-free sample preparation techniques and bioinformatic enrichment analysis to in depth characterise the cell wall proteome of mycobacteria

机译:无凝胶样品制备技术和生物信息学富集分析可深入表征分枝杆菌的细胞壁蛋白质组

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摘要

The comprehensive characterisation of the cell wall proteome of mycobacteria is of considerable relevance to both the discovery of new drug targets as well as to the design of new vaccines againstMycobacterium tuberculosis. However, due to its extremely hydrophobic nature, the coverage of proteomic studies of this subcellular compartment is still far from complete. Here, we report novel gel-free cell wall sample preparation procedures and quantitative LC–MS/MS measurements on a Q Exactive mass spectrometer. We combine these with a novel post-measurement bioinformatic analysis to filter out likely cytosolic contaminants. This reveals a subset of proteins that are highly enriched for cell wall proteins. The success of this approach is verified by peptide-centric measurement of the abundance of known subcellular markers, as well as analysis of the percentage of predicted membrane proteins within the purified fraction. WhileM. smegmatiswas used during this study to establish and optimise the sample preparation procedures, these can easily be applied to other mycobacterial species, such asM. bovisBCG orM. tuberculosis.?Improved gel-free cell wall sample preparation gives higher yields of tryptic peptides for LC–MS/MS measurement.?Higher yields of tryptic peptides provide better quantitation and coverage of cell wall proteome.?Post-measurement enrichment analysis filters out high abundance cytosolic contaminants that have carried through the experimental analysis.
机译:分枝杆菌细胞壁蛋白质组的全面表征与新药靶标的发现以及针对结核分枝杆菌的新疫苗的设计均具有相当的相关性。然而,由于其极其疏水的性质,对该亚细胞区室的蛋白质组学研究的覆盖范围仍然远远不够。在这里,我们报告了新型无凝胶细胞壁样品制备程序以及在Q Exactive质谱仪上进行的定量LC-MS / MS测量。我们将这些与新颖的测量后生物信息学分析相结合,以过滤出可能的胞质污染物。这揭示了高度富集细胞壁蛋白质的蛋白质子集。通过以肽为中心的已知亚细胞标记物丰度的测量以及分析纯化级分中预测的膜蛋白的百分比,可以验证这种方法的成功。 WhileM。在这项研究期间,使用耻垢分枝杆菌来建立和优化样品制备程序,这些可以很容易地应用于其他分枝杆菌物种,例如M。 bovisBCG orM。结核病。改进的无凝胶细胞壁样品制备方法可提高LC-MS / MS测量的胰蛋白酶肽的产量。较高的胰蛋白酶肽的产量可提供更好的细胞壁蛋白质组定量和覆盖范围。通过实验分析得出的大量胞质污染物。

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