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基于金纳米粒子作为信号转导探针的高灵敏电致化学发光生物传感器用于蛋白质激酶活性及抑制分析。

Highly sensitive electrogenerated chemiluminescence biosensor in profiling protein kinase activity and inhibition using gold nanoparticle as signal transduction probes.

机构信息

Department of Chemistry, Key Lab of Bioorganic Phosphorus Chemistry and Chemical Biology, Tsinghua University, Beijing 100084, China.

出版信息

Anal Chem. 2010 Nov 15;82(22):9566-72. doi: 10.1021/ac102296g. Epub 2010 Oct 26.

DOI:10.1021/ac102296g
PMID:20977199
Abstract

A novel electrogenerated chemiluminescence (ECL) biosensor using gold nanoparticles as signal transduction probes was described for the detection of kinase activity. The gold nanoparticles were specifically conjugated to the thiophosphate group after the phosphorylation process in the presence of adenosine 59-[c-thio] triphosphate (ATP-s) cosubstrate. Due to its good conductivity, large surface area, and excellent electroactivity to luminol oxidization, the gold nanoparticles extremely amplified the ECL signal of luminol, offering a highly sensitive ECL biosensor for kinase activity detection. Protein kinase A (PKA), an important enzyme in regulation of glycogen, sugar, and lipid metabolism in the human body, was used as a model to confirm the proof-of-concept strategy. The as-proposed biosensor presented high sensitivity, low detection limit of 0.07 U mL(-1), wide linear range (from 0.07 to 32 U mL(-1)), and excellent stability. Moreover, this biosensor can also be used for quantitative analysis of kinase inhibition. On the basis of the inhibitor concentration dependent ECL signal, the half-maximal inhibition value IC(50) of ellagic acid, a PKA inhibitor, was estimated, which was in agreement with those characterized with the conventional kinase assay. While nearly no ECL signal change can be observed in the presence of Tyrphostin AG1478, a tyrosine kinase inhibitor, but not PKA inhibitor, shows its excellent performance in kinase inhibitor screening. The simple and sensitive biosensor is promising in developing a high-through assay of in vitro kinase activity and inhibitor screening for clinic diagnostic and drug development.

摘要

一种新型的电致化学发光(ECL)生物传感器,使用金纳米粒子作为信号转导探针,用于检测激酶活性。在存在腺苷 59-[c-硫]三磷酸(ATP-s)共底物的情况下,金纳米粒子在磷酸化过程后被特异性地连接到硫代磷酸基团上。由于其良好的导电性、大的表面积和对鲁米诺氧化的优异电活性,金纳米粒子极大地放大了鲁米诺的 ECL 信号,为激酶活性检测提供了一种高灵敏度的 ECL 生物传感器。蛋白激酶 A(PKA)是人体内调节糖原、糖和脂质代谢的重要酶,被用作模型来证实这一概念验证策略。所提出的生物传感器具有高灵敏度、低检测限为 0.07 U mL(-1)、宽线性范围(从 0.07 到 32 U mL(-1))和出色的稳定性。此外,该生物传感器还可用于定量分析激酶抑制剂。基于抑制剂浓度依赖的 ECL 信号,估算了 PKA 抑制剂鞣花酸的半数最大抑制值 IC(50),与传统激酶测定法得到的结果一致。而在存在酪氨酸激酶抑制剂 Tyrphostin AG1478 的情况下,几乎观察不到 ECL 信号变化,但不是 PKA 抑制剂,这表明其在激酶抑制剂筛选中具有出色的性能。这种简单而灵敏的生物传感器有望用于开发体外激酶活性的高通量检测和用于临床诊断和药物开发的抑制剂筛选。

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