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蛋白质的快速光化学氧化与多维蛋白质鉴定技术(MudPIT)联用:将足迹策略扩展至复杂系统

Fast photochemical oxidation of proteins coupled to multidimensional protein identification technology (MudPIT): expanding footprinting strategies to complex systems.

作者信息

Rinas Aimee, Jones Lisa M

机构信息

Department of Chemistry and Chemical Biology, Indiana University-Purdue University Indianapolis, Indianapolis, IN, 46202, USA.

出版信息

J Am Soc Mass Spectrom. 2015 Apr;26(4):540-6. doi: 10.1007/s13361-014-1017-6. Epub 2014 Nov 20.

DOI:10.1007/s13361-014-1017-6
PMID:25409907
Abstract

Peptides containing the oxidation products of hydroxyl radical-mediated protein footprinting experiments are typically much less abundant than their unoxidized counterparts. This is inherent to the design of the experiment as excessive oxidation may lead to undesired conformational changes or unfolding of the protein, skewing the results. Thus, as the complexity of the systems studied using this method expands, the detection and identification of these oxidized species can be increasingly difficult with the limitations of data-dependent acquisition (DDA) and one-dimensional chromatography. Here we report the application of multidimensional protein identification technology (MudPIT) in combination with hydroxyl radical footprinting as a method to increase the identification of quantifiable peptides in these experiments. Using this method led to a 37% increase in unique peptide identifications as well as a 70% increase in protein group identifications over one-dimensional data-dependent acquisition on the same samples. Furthermore, we demonstrate the combination of these methods as a means to investigate megadalton complexes.

摘要

含有羟基自由基介导的蛋白质足迹实验氧化产物的肽通常比其未氧化的对应物丰度低得多。这是实验设计所固有的,因为过度氧化可能导致蛋白质出现不期望的构象变化或展开,从而使结果产生偏差。因此,随着使用该方法研究的系统复杂性增加,基于数据依赖采集(DDA)和一维色谱的局限性,检测和鉴定这些氧化物种可能会越来越困难。在此,我们报告了多维蛋白质鉴定技术(MudPIT)与羟基自由基足迹相结合的应用,作为一种在这些实验中增加可定量肽鉴定的方法。使用该方法使得独特肽鉴定增加了37%,并且与对相同样品进行一维数据依赖采集相比,蛋白质组鉴定增加了70%。此外,我们证明了这些方法的结合可作为研究兆道尔顿复合物的一种手段。

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