Harold C, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center at Dallas, Dallas, TX 75390, USA.
Proteome Sci. 2011 Sep 15;9:53. doi: 10.1186/1477-5956-9-53.
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.
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。