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Beads-free protein immunoprecipitation for a mass spectrometry-based interactome and posttranslational modifications analysis

机译:用于基于质谱的相互作用组和翻译后修饰分析的无珠蛋白免疫沉淀

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Background Protein immunoprecipitation (IP) coupled with MS provides means to interrogate protein complexes and their posttranslational modifications (PTMs). In a typical protein IP assay antibodies are conjugated to protein A/G beads requiring large amounts of antibodies, tube transfers and centrifugations. Results As an alternative, we present Matrix-IP, beads-free microplate-based platform with surface-immobilized antibodies. Assay utilizes standard 96-well polypropylene PCR plates that are laboratory-fabricated with UV-C light and then protein A/G coated prior to IP reaction. We demonstrate application of Matrix-IP platform in MS analysis of heterogeneous nuclear ribonucleoprotein K (hnRNP K) interactome and PTMs. Conclusion Matrix-IP is time-saving, easy to use high throughput method adaptable for low sample amounts and automation.
机译:背景技术与MS结合的蛋白质免疫沉淀(IP)提供了询问蛋白质复合物及其翻译后修饰(PTM)的方法。在典型的蛋白质IP分析中,抗体与蛋白质A / G珠缀合,需要大量抗体,试管转移和离心。结果作为替代方案,我们提出了具有表面固定抗体的基于Matrix-IP,无珠的基于微孔板的平台。该测定法使用标准的96孔聚丙烯PCR板,该板在实验室用UV-C光源制成,然后在IP反应之前将蛋白A / G包被。我们展示了Matrix-IP平台在异构核糖核糖核蛋白K(hnRNP K)相互作用组和PTM的MS分析中的应用。结论Matrix-IP节省时间,易于使用的高通量方法,适用于低样品量和自动化。

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