首页> 美国卫生研究院文献>MethodsX >Gel-free sample preparation techniques and bioinformatic enrichment analysis to in depth characterise the cell wall proteome of mycobacteria
【2h】

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

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

class="kwd-title">Method name: Cell wall enrichment and bioinformatic enrichment analysis class="kwd-title">Keywords: Cell wall proteomics, Mycobacteria, Proteomics, Bioinformatic enrichment analysis class="head no_bottom_margin" id="abs0010title">AbstractThe 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 against Mycobacterium 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. While M. smegmatis was used during this study to establish and optimise the sample preparation procedures, these can easily be applied to other mycobacterial species, such as M. bovis BCG or M. tuberculosis. class="first-line-outdent" id="lis0005">
  • • 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:<!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchred” f5-> <!-fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> class =“ kwd-title”>方法名称:细胞壁富集和生物信息学富集分析 class =“ kwd-title”>关键字:< / strong>细胞壁蛋白质组学,分枝杆菌,蛋白质组学,生物信息学富集分析 class =“ head no_bottom_margin” id =“ abs0010title”>摘要分枝杆菌细胞壁蛋白质组的全面表征与这两种方法都有着重要的联系。发现新的药物靶标以及设计针对结核分枝杆菌的新疫苗。然而,由于其极强的疏水性,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。尽管在这项研究中使用耻垢分枝杆菌来建立和优化样品制备程序,但这些方法可以轻松应用于其他分枝杆菌物种,例如牛分枝杆菌BCG或结核分枝杆菌。 class =“ first-line-outdent” id =“ lis0005”> <!-list-behavior =简单的前缀-word = mark-type = none max-label-size = 9->
  • •改进的无凝胶细胞壁样品制备具有较高收率的胰蛋白酶肽用于LC-MS / MS测量。
  • •较高收率的胰蛋白酶肽可以更好地定量和覆盖细胞壁蛋白质组。
  • •测量后的富集分析可以过滤掉通过实验分析而产生的高丰度胞质污染物。
  • 著录项

    相似文献

    • 外文文献
    • 中文文献
    • 专利
    代理获取

    客服邮箱:kefu@zhangqiaokeyan.com

    京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
    • 客服微信

    • 服务号