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An Improved 2-Dimensional Gel Electrophoresis Method for Resolving Human Erythrocyte Membrane Proteins

机译:改进的二维凝胶电泳方法解析人红细胞膜蛋白

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摘要

The 2-dimensional gel electrophoresis (2-DE) technique is widely used for the analysis of complex protein mixtures extracted from biological samples. It is one of the most commonly used analytical techniques in proteomics to study qualitative and quantitative protein changes between different states of a cell or an organism (eg, healthy and diseased), conditionally expressed proteins, posttranslational modifications, and so on. The 2-DE technique is used for its unparalleled ability to separate thousands of proteins simultaneously. The resolution of the proteins by 2-DE largely depends on the quality of sample prepared during protein extraction which increases results in terms of reproducibility and minimizes protein modifications that may result in artifactual spots on 2-DE gels. The buffer used for the extraction and solubilization of proteins influences the quality and reproducibility of the resolution of proteins on 2-DE gel. The purification by cleanup kit is another powerful process to prevent horizontal streaking which occurs during isoelectric focusing due to the presence of contaminants such as salts, lipids, nucleic acids, and detergents. Erythrocyte membrane proteins serve as prototypes for multifunctional proteins in various erythroid and nonerythroid cells. In this study, we therefore optimized the selected major conditions of 2-DE for resolving various proteins of human erythrocyte membrane. The modification included the optimization of conditions for sample preparation, cleanup of protein sample, isoelectric focusing, equilibration, and storage of immobilized pH gradient strips, which were further carefully examined to achieve optimum conditions for improving the quality of protein spots on 2-DE gels. The present improved 2-DE analysis method enabled better detection of protein spots with higher quality and reproducibility. Therefore, the conditions established in this study may be used for the 2-DE analysis of erythrocyte membrane proteins for different diseases, which may help to identify the proteins that may serve as markers for diagnostics as well as targets for development of new therapeutic potential.
机译:二维凝胶电泳(2-DE)技术被广泛用于分析从生物样品中提取的复杂蛋白混合物。它是蛋白质组学中最常用的分析技术之一,用于研究细胞或生物体不同状态(例如健康和患病),有条件表达的蛋白质,翻译后修饰等之间的定性和定量蛋白质变化。 2-DE技术具有无与伦比的能力,可同时分离数千种蛋白质。 2-DE对蛋白质的分辨率在很大程度上取决于在蛋白质提取过程中制备的样品的质量,这会提高可重复性的结果,并最大程度地减少可能导致2-DE凝胶上人为斑点的蛋白质修饰。用于提取和溶解蛋白质的缓冲液会影响2-DE凝胶上蛋白质分辨率的质量和重现性。通过清洁套件进行纯化是另一种有效的过程,可防止由于存在盐,脂质,核酸和去污剂等污染物而在等电聚焦过程中发生水平条纹。红细胞膜蛋白是各种红系和非红系细胞中多功能蛋白的原型。因此,在这项研究中,我们优化了选择2-DE的主要条件,以解析人红细胞膜的各种蛋白质。修改内容包括优化样品制备条件,蛋白质样品净化,等电聚焦,平衡和固定化pH梯度条的存储,进一步仔细检查这些条件以获得改善2-DE凝胶上蛋白质斑点质量的最佳条件。本发明的改进的2-DE分析方法能够更好地检测具有更高质量和再现性的蛋白质斑点。因此,本研究建立的条件可用于针对不同疾病的红细胞膜蛋白进行2-DE分析,这可能有助于鉴定可用作诊断标志物以及开发新治疗潜力的靶标的蛋白。

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