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首页> 外文期刊>Proteomics >Analysis of Human Proteome Organization Plasma Proteome Project (HUPO PPP) reference specimens using surface enhanced laser desorption/ionization-time of flight (SELDI-TOF) mass spectrometry: Multi-institution correlation of spectra and identificatio
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Analysis of Human Proteome Organization Plasma Proteome Project (HUPO PPP) reference specimens using surface enhanced laser desorption/ionization-time of flight (SELDI-TOF) mass spectrometry: Multi-institution correlation of spectra and identificatio

机译:使用表面增强激光解吸/电离飞行时间(SELDI-TOF)质谱分析人类蛋白质组组织血浆蛋白质组计划(HUPO PPP)参考标本:光谱和鉴定的多机构关联

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摘要

We report on a multicenter analysis of HUPO reference specimens using SELDI-TOF MS. Eight sites submitted data obtained from serum and plasma reference specimen analysis. Spectra from five sites passed preliminary quality assurance tests and were subjected to further analysis. Intralaboratory CVs varied from 15 to 43%. A correlation coefficient matrix generated using data from these five sites demonstrated high level of correlation, with values > 0.7 on 37 of 42 spectra. More than 50 peaks were differentially present among the various sample types, as observed on three chip surfaces. Additionally, peaks at similar to 9200 and similar to 15950 m/z were present only in select reference specimens. Chromatographic fractionation using anion-exchange, membrane cutoff, and reverse phase chromatography, was employed for protein purification of the similar to 9200 m/z peak. It was identified as the haptoglobin alpha subunit after peptide mass fingerprinting and high-resolution MS/MS analysis. The differential expression of this protein was confirmed by Western blot analysis. These pilot studies demonstrate the potential of the SELDI platform for reproducible and consistent analysis of serum/plasma across multiple sites and also for targeted biomarker discovery and protein identification. This approach could be exploited for population-based studies in all phases of the HUPO PPP.
机译:我们报告了使用SELDI-TOF MS对HUPO参考样本进行的多中心分析。八个站点提交了从血清和血浆参考样本分析获得的数据。来自五个地点的光谱通过了初步的质量保证测试,并进行了进一步分析。实验室内简历的比例从15%到43%不等。使用来自这五个位置的数据生成的相关系数矩阵显示出很高的相关性,在42个光谱中的37个光谱上的值> 0.7。如在三个芯片表面上所观察到的,在各种样品类型中,有超过50个峰存在差异。此外,仅在选定的参考样本中出现了类似于9200和类似于15950 m / z的峰。使用阴离子交换色谱法,膜截止色谱法和反相色谱法进行色谱分离,以纯化类似于9200 m / z峰的蛋白质。经过肽质量指纹分析和高分辨率MS / MS分析后,它被鉴定为触珠蛋白α亚基。通过蛋白质印迹分析证实了该蛋白质的差异表达。这些先导研究证明了SELDI平台具有潜力,可对多个部位的血清/血浆进行可重复且一致的分析,还可用于靶向生物标志物的发现和蛋白质鉴定。在HUPO PPP的所有阶段,都可以将这种方法用于基于人群的研究。

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