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通过制备性电泳结合双向电泳对人尿蛋白质组进行表征。

Characterization of the human urine proteome by preparative electrophoresis in combination with 2-DE.

作者信息

Zerefos Panagiotis G, Vougas Konstantinos, Dimitraki Ploumisti, Kossida Sophia, Petrolekas Andreas, Stravodimos Konstantinos, Giannopoulos Aris, Fountoulakis Michael, Vlahou Antonia

机构信息

Division of Biotechnology, Foundation for Biomedical Research of the Academy of Athens, Greece.

出版信息

Proteomics. 2006 Aug;6(15):4346-55. doi: 10.1002/pmic.200500671.

Abstract

The protein components of urine are useful indicators of renal function and human health in general. Urine samples are easily attainable making them ideal substrates for biomarker research. Analysis of the urine proteome however, has been hindered by the great variability of the urine specimens, and the presence of various proteins in low abundance or modified forms. To alleviate some of these problems urine samples from five different individuals were pooled, concentrated and the proteome characterized by a combination of preparative electrophoresis and 2-DE, followed by PMF. A total of 778 protein spots corresponding to 141 different gene products were identified. In comparison, 171 spots corresponding to 44 unique proteins were identified in the unfractionated starting material. Among the proteins identified from the preparative electrophoresis were many of low abundance such as proteins involved in signal transduction. Furthermore, the median molecular mass of the identified proteins from the preparative electrophoresis was significantly lower in comparison to the proteins identified from the unfractionated starting material (39 886 Da versus 71 317 Da, respectively). Concluding, application of this methodology provides a coherent analysis of the urine proteome and contributes to the generation of the urine protein map in health and disease.

摘要

尿液中的蛋白质成分通常是肾功能和人体健康的有用指标。尿液样本易于获取,使其成为生物标志物研究的理想底物。然而,尿液蛋白质组的分析受到尿液样本巨大变异性以及各种低丰度或修饰形式蛋白质存在的阻碍。为了缓解其中一些问题,将来自五个不同个体的尿液样本混合、浓缩,并通过制备电泳和二维电泳相结合的方法对蛋白质组进行表征,随后进行肽质量指纹图谱分析。共鉴定出对应于141种不同基因产物的778个蛋白质斑点。相比之下,在未分级的起始材料中鉴定出对应于44种独特蛋白质的171个斑点。从制备电泳中鉴定出的蛋白质中有许多是低丰度的,例如参与信号转导的蛋白质。此外,与从未分级起始材料中鉴定出的蛋白质相比,从制备电泳中鉴定出的蛋白质的中位分子量显著更低(分别为39886 Da和71317 Da)。总之,这种方法的应用为尿液蛋白质组提供了连贯的分析,并有助于生成健康和疾病状态下的尿液蛋白质图谱。

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