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用于定量植物蛋白质组学的整株植物水培同位素标记法(HILEP);氧化应激案例研究

Hydroponic isotope labelling of entire plants (HILEP) for quantitative plant proteomics; an oxidative stress case study.

作者信息

Bindschedler Laurence V, Palmblad Magnus, Cramer Rainer

机构信息

The BioCentre, The University of Reading, Reading, UK.

出版信息

Phytochemistry. 2008 Jul;69(10):1962-72. doi: 10.1016/j.phytochem.2008.04.007. Epub 2008 Jun 5.

Abstract

Hydroponic isotope labelling of entire plants (HILEP) is a cost-effective method enabling metabolic labelling of whole and mature plants with a stable isotope such as (15)N. By utilising hydroponic media that contain (15)N inorganic salts as the sole nitrogen source, near to 100% (15)N-labelling of proteins can be achieved. In this study, it is shown that HILEP, in combination with mass spectrometry, is suitable for relative protein quantitation of seven week-old Arabidopsis plants submitted to oxidative stress. Protein extracts from pooled (14)N- and (15)N-hydroponically grown plants were fractionated by SDS-PAGE, digested and analysed by liquid chromatography electrospray ionisation tandem mass spectrometry (LC-ESI-MS/MS). Proteins were identified and the spectra of (14)N/(15)N peptide pairs were extracted using their m/z chromatographic retention time, isotopic distributions, and the m/z difference between the (14)N and (15)N peptides. Relative amounts were calculated as the ratio of the sum of the peak areas of the two distinct (14)N and (15)N peptide isotope envelopes. Using Mascot and the open source trans-proteomic pipeline (TPP), the data processing was automated for global proteome quantitation down to the isoform level by extracting isoform specific peptides. With this combination of metabolic labelling and mass spectrometry it was possible to show differential protein expression in the apoplast of plants submitted to oxidative stress. Moreover, it was possible to discriminate between differentially expressed isoforms belonging to the same protein family, such as isoforms of xylanases and pathogen-related glucanases (PR 2).

摘要

整株植物的水培同位素标记法(HILEP)是一种经济高效的方法,能够使用诸如(15)N等稳定同位素对完整且成熟的植物进行代谢标记。通过利用含有(15)N无机盐作为唯一氮源的水培介质,可实现接近100%的蛋白质(15)N标记。在本研究中,结果表明,HILEP与质谱联用适用于对遭受氧化应激的七周龄拟南芥植株进行相对蛋白质定量分析。将水培生长的(14)N和(15)N植株的蛋白质提取物进行SDS-PAGE分级分离、消化,然后通过液相色谱电喷雾电离串联质谱(LC-ESI-MS/MS)进行分析。鉴定蛋白质,并利用其质荷比、色谱保留时间、同位素分布以及(14)N和(15)N肽段之间的质荷比差异提取(14)N/(15)N肽对的光谱。相对含量计算为两种不同的(14)N和(15)N肽同位素包络峰面积之和的比值。使用Mascot和开源的跨蛋白质组学管道(TPP),通过提取异构体特异性肽段,实现了数据处理自动化,可对全局蛋白质组进行定量分析,直至异构体水平。通过这种代谢标记与质谱联用的方法,能够显示遭受氧化应激的植物质外体中蛋白质的差异表达。此外,还能够区分属于同一蛋白质家族的差异表达异构体,如木聚糖酶和病程相关葡聚糖酶(PR 2)的异构体。

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