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使用微斑点免疫测定法对磷蛋白进行定量分析。

Quantitative analysis of phosphoproteins using microspot immunoassays.

作者信息

Henjes Frauke, Götschel Frank, Jöcker Anika, Korf Ulrike

机构信息

Division of Molecular Genome Analysis, German Cancer Research Center (DKFZ), Heidelberg, Germany.

出版信息

Methods Mol Biol. 2011;785:191-201. doi: 10.1007/978-1-61779-286-1_13.

Abstract

Protein microarrays are an ideal technology platform which allow for a robust and standardized profiling of the cellular proteome. Many cellular functions are not simply controlled by the presence of certain proteins, especially the propagation of external stimuli, which depend on transient post-translational modifications that determine whether a protein is in its active or inactive state. Thus, complex biological processes require the availability of a sound set of quantitative and time-resolved measurements to be understood. For this reason, new assay platforms which allow for the investigation of several proteins in parallel are necessary. The current best understood mode of cellular regulation occurs via phosphorylation and dephosphorylation processes, which are mediated via a large panel of kinases and phosphatases. The microspot immunoassay technique described here allows for an exact determination of several different phosphorylated proteins in parallel, as well as from small sample amounts, and is therefore an appropriate system to deepen the understanding of the complex regulatory networks implicated in health and disease.

摘要

蛋白质微阵列是一种理想的技术平台,可对细胞蛋白质组进行强大且标准化的分析。许多细胞功能并非简单地由某些蛋白质的存在所控制,特别是外部刺激的传播,这取决于瞬时翻译后修饰,这些修饰决定了蛋白质处于活性还是非活性状态。因此,复杂的生物过程需要一系列完善的定量和时间分辨测量才能被理解。出于这个原因,需要新的检测平台来并行研究多种蛋白质。目前对细胞调节理解最透彻的模式是通过磷酸化和去磷酸化过程发生的,这些过程由大量的激酶和磷酸酶介导。本文所述的微斑点免疫测定技术能够并行且从小样本量中精确测定几种不同的磷酸化蛋白质,因此是一个加深对健康和疾病中复杂调控网络理解的合适系统。

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