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Titlebook: Kinase Signaling Networks; Aik-Choon Tan,Paul H. Huang Book 2017 Springer Science+Business Media, LLC, part of Springer Nature 2017 Protei

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Dissecting Kinase Effector Signaling Using the RapRTAP Methodologyplex in living cells. This technology uses a rapamycin-inducible kinase activation coupled to interaction with FKBP12-binding domain (FRB) tagged protein. Here, we demonstrate application of this method by targeting Src to either p130Cas or FAK and discriminating cell mophodynamic changes downstream each of these signaling complexes.
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Proteomic Profiling of Protein Kinase Inhibitor Targets by Mass Spectrometryan example, we provide an optimized protocol featuring on-bead protein digestion and single nano-flow liquid chromatographic-mass spectrometric (LC-MS) analyses, consequently increasing analytical throughput and sensitivity over gel-based sample preparation methods for rapid profiling of kinase inhibitor targets.
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Analysis of Phosphotyrosine Signaling Networks in Lung Cancer Cell Linesust two-stage isolation of phosphotyrosine peptides and mass spectrometry-aided identification of phosphosites to characterize basal signaling networks in unstimulated non-small cell lung cancer (NSCLC) cell lines.
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Dissecting Kinase Effector Signaling Using the RapRTAP Methodologyponse. Dissecting downstream signaling pathways of kinases is a key step to understanding physiological and pathological cell process. However, directing kinase activity to specific substrates remains challenging. Here, we present a new tool to selectively activate a kinase in a specific protein com
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Quantification of Cell Signaling Networks Using Kinase Activity Chemosensors disease phenotypes. When activity data is collected across a panel of kinases, a unique “signaling fingerprint” is generated that allows for discrimination between diseased and normal tissue. Here we describe the use of peptide-based kinase activity sensors to fingerprint the signaling changes asso
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