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Microarray-based Raman spectroscopic assay for kinase inhibition by gold nanoparticle probes

机译:基于微阵列的拉曼光谱测定法用于金纳米粒子探针抑制激酶

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摘要

In this paper, a microarray-based surface-enhanced Raman spectroscopic (SERS) assay for detection of kinase functionality and inhibition has been reported. Biotinylated anti-phosphoserinen antibodies mark the phosphorylation and inhibition events and gold nanoparticles are attached to the antibodies by standard avidin-biotin chemistry, followed by silver deposition for SERS signal enhancement. The avidin conjugated fluorescein is used as SERS probe. The alpha-catalytic subunit of cyclic adenosine 5'-monophosphate (cAMP) dependent protein kinase (PKA), its well known substrate, kemptide, and three inhibitors, H89, HA1077, and KN62 have been chosen here to establish the SERS assay. As expected, highly selective inhibition of PKA is demonstrated with the inhibitor H89 and the inhibition assay enable to detect kinase inhibition as well as derive IC50 (half maximal inhibitory concentration) plots.
机译:在本文中,已经报道了基于微阵列的表面增强拉曼光谱(SERS)检测法,用于检测激酶功能和抑制作用。生物素化的抗磷酸丝氨酸碱抗体标记磷酸化和抑制事件,金纳米颗粒通过标准抗生物素蛋白-生物素化学方法附着在抗体上,然后沉积银以增强SERS信号。将抗生物素蛋白缀合的荧光素用作SERS探针。此处选择了环状腺苷5'-单磷酸(cAMP)依赖性蛋白激酶(PKA)的α-催化亚基,其众所周知的底物,肯普肽和三种抑制剂H89,HA1077和KN62来建立SERS分析。如预期的那样,用抑制剂H89证明了对PKA的高度选择性抑制,并且抑制分析能够检测激酶抑制以及得出IC50(半数最大抑制浓度)图。

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