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改进的蛋白质芯片用于定量系统分析信号通路相互作用的动态

Improved protein arrays for quantitative systems analysis of the dynamics of signaling pathway interactions.

机构信息

Harold C, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center at Dallas, Dallas, TX 75390, USA.

出版信息

Proteome Sci. 2011 Sep 15;9:53. doi: 10.1186/1477-5956-9-53.

Abstract

An improved version of quantitative protein array platform utilizing linear Quantum dot signaling for systematically measuring protein levels and phosphorylation states is presented. The signals are amplified linearly by a confocal laser Quantum dot scanner resulting in ~1000-fold more sensitivity than traditional Western blots, but are not linear by the enzyme-based amplification. Software is developed to facilitate the quantitative readouts of signaling network activities. Kinetics of EGFRvIII mutant signaling was analyzed to quantify cross-talks between EGFR and other signaling pathways.

摘要

本文介绍了一种改进的定量蛋白质芯片平台,该平台利用线性量子点信号来系统地测量蛋白质水平和磷酸化状态。通过共焦激光量子点扫描仪对信号进行线性放大,比传统的 Western blot 方法灵敏约 1000 倍,但酶放大方法不是线性的。开发了软件来促进信号网络活性的定量读数。分析了 EGFRvIII 突变信号的动力学,以量化 EGFR 与其他信号通路之间的串扰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d228/3182966/81fe819440d3/1477-5956-9-53-1.jpg

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