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Pull-down Assay on Streptavidin Beads and Surface Plasmon Resonance Chips for SWATH-MS-based Interactomics

机译:基于SWATH-MS的相互作用的链霉亲和素珠和表面等离振子共振芯片的下拉测定

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摘要

Background/Aim: Pul-down assay is a popular in vitro method for identification of physical interactors of selected proteins. Here, for the first time, we compared three conventional variants of pull-down assay with the streptavidin-modified surface plasmon resonance (SPR) chips for the detection of PDZ and LIM domain protein 2 (PDLIM2) interaction partners. Materials and Methods: PDLIM2 protein–protein interactions were analysed by three variants of pull-down assay on streptavidin beads using LC-MS/MS in “Sequential Window Acquisition of all Theoretical fragment ion spectra (SWATH)” mode and compared with LC-SWATH-MS/MS data from SPR chips. Results: The results showed that (i) the use of SPR chip led to comparable data compared to on-column streptavidin beads, (ii) gravity flow and microflow in wash and elution steps provided better results than centrifugation, and (iii) type and concentration of detergent did not significantly affect the interactome data of cancer-associated PDLIM2. Conclusion: Our study supports further application of SPR-based affinity purification with SWATH mass spectrometry for reproducible and controlled characterization of cancer-associated interactomes.
机译:背景/目的:下拉测定法是一种流行的体外方法,用于鉴定所选蛋白质的物理相互作用物。在这里,我们第一次比较了下拉测定法的三种常规变体与链霉亲和素修饰的表面等离振子共振(SPR)芯片,用于检测PDZ和LIM域蛋白2(PDLIM2)相互作用的伴侣。材料和方法:使用LC-MS / MS在“所有理论碎片离子光谱的顺序窗口采集”模式下,通过链霉亲和素珠的三种下拉测定法分析了PDLIM2蛋白之间的相互作用,并与LC-SWATH进行了比较-来自SPR芯片的MS / MS数据。结果:结果表明:(i)与柱上抗生蛋白链菌素珠相比,使用SPR芯片可获得可比的数据;(ii)洗涤和洗脱步骤中的重力流和微流比离心提供了更好的结果;(iii)类型和去污剂的浓度不会显着影响癌症相关的PDLIM2的相互作用组数据。结论:我们的研究支持SWATH质谱法基于SPR的亲和纯化在癌症相关相互作用组的可再现和受控表征中的进一步应用。

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