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Studying chemical-regulation of intracellular kinase activity by peptide microarray-based assay with gold nanoparticle probes

机译:用金纳米颗粒探针通过基于肽微阵列的测定研究细胞内激酶活性的化学调节

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In the present work, the chemical regulation of intracellular kinase activity has been studied by a peptide microarray-based resonance light scattering (RLS) assay with gold nanoparticle (AuNP) probes. After interactions of five cell lines and seven compounds (six potential inhibitors of cyclic adenosine monophosphate (cAMP)-dependent protein kinase A (PKA) and Forskolin (Fsk)), we found that the intracellular PKA activity is strongly regulated by the extracellular compounds and that the compounds affect the intracellular PKA activity in a dose-dependent manner. The experimental results demonstrate that the peptide microarray-based RLS assay can be employed to quantitatively determine the efficiency of the inhibitor/activator on the kinase activity at the cellular level. In addition, chemical-mediated fluctuation of the PKA activity in different cell phases (e.g., G2/M phase and M/G1 phase) was successfully detected, which also demonstrates the utility of the approach for monitoring chemical regulation of intracellular kinase activity.
机译:在本工作中,已经通过金纳米粒子(AuNP)探针基于肽微阵列的共振光散射(RLS)分析研究了细胞内激酶活性的化学调控。在五种细胞系和七种化合物(六种潜在的环磷酸单腺苷(cAMP)依赖性蛋白激酶A(PKA)和福斯高林(Fsk)抑制剂)相互作用后,我们发现细胞内PKA活性受到细胞外化合物的强烈调节,并且这些化合物以剂量依赖的方式影响细胞内PKA活性。实验结果表明,基于肽微阵列的RLS分析可用于在细胞水平上定量确定抑制剂/活化剂对激酶活性的效率。另外,成功地检测到在不同细胞相(例如,G2 / M相和M / G1相)中PKA活性的化学介导的波动,这也证明了该方法用于监测细胞内激酶活性的化学调节的实用性。

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