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首页> 外文期刊>Analytical chemistry >Graphene Oxide-Peptide Nanocomplex as a Versatile Fluorescence Probe of Protein Kinase Activity Based on Phosphorylation Protection against Carboxypeptidase Digestion
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Graphene Oxide-Peptide Nanocomplex as a Versatile Fluorescence Probe of Protein Kinase Activity Based on Phosphorylation Protection against Carboxypeptidase Digestion

机译:氧化石墨烯-肽纳米复合物作为蛋白激酶活性的多功能荧光探针,基于磷酸化对羧肽酶消化的保护作用

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摘要

The research on complicated kinomics and kinase-target drug discovery requires the development of simple, cost-effective, and multiplex kinase assays. Herein, we propose a novel and versatile biosensing platform for the detection of protein kinase activity based on graphene oxide (GO)-peptide nanocomplex and phosphorylation-induced suppression of carboxypeptidase Y (CPY) cleavage. Kinasecatalyzed phosphorylation protects the fluorophore-labeled peptide probe against CPY digestion and induces the formation of a GO/peptide nanocomplex resulting in fluorescence quenching, while the nonphosphopeptide is degraded by CPY to release free fluorophore as well as restore fluorescence. This GO-based nanosensor has been successfully applied to sensitively detect two model kinases, casein kinase (CKII) and cAMP-dependent protein kinase (PKA) with low detection limits of 0.0833 mU/μL and 0.134 mU/μL, respectively. The feasibility of this GO-based sensor was further demonstrated by the assessment of kinase inhibition by staurosporine and H-89, in vitro kinase assay in cell lysates, and simultaneous detection of CKII and PKA activity. Moreover, the GO-based fluorescence anisotropy (FA) kinase assay has been also developed using GO as a FA signal amplifier. The proposed sensor is homogeneous, facile, universal, label-free, and applicable for multiplexed kinase assay, presenting a promising method for kinase-related biochemical fundamental research and inhibitor screening.
机译:有关复杂的动力学和激酶靶点药物发现的研究要求开发简单,经济高效的多重激酶测定法。在这里,我们提出了一种新颖而通用的生物传感平台,用于基于氧化石墨烯(GO)-肽纳米复合物和磷酸化诱导的羧肽酶Y(CPY)裂解抑制蛋白激酶活性的检测。激酶催化的磷酸化作用可保护荧光团标记的肽探针免受CPY消化并诱导GO /肽纳米复合物的形成,从而导致荧光猝灭,而非磷酸肽则被CPY降解以释放出游离荧光团并恢复荧光。这种基于GO的纳米传感器已成功应用于灵敏地检测两种模型激酶,酪蛋白激酶(CKII)和cAMP依赖性蛋白激酶(PKA),其低检出限分别为0.0833 mU /μL和0.134 mU /μL。通过评估星形孢菌素和H-89对激酶的抑制作用,细胞裂解物中的体外激酶测定以及同时检测CKII和PKA活性,进一步证明了这种基于GO的传感器的可行性。此外,还已经使用GO作为FA信号放大器开发了基于GO的荧光各向异性(FA)激酶测定法。拟议的传感器是同质,方便,通用,无标签,并适用于多重激酶测定,为激酶相关的生化基础研究和抑制剂筛选提供了一种有前途的方法。

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