School of Life Science and Technology, Huazhong University of Science and Technology Wuhan, Hubei, 430074, China.
Department of Hepatobiliary Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Biosens Bioelectron. 2019 Oct 1;142:111494. doi: 10.1016/j.bios.2019.111494. Epub 2019 Jul 5.
Almost no analytical assays, either colorimetric or fluorescence assays, for generic microplate readers is capable of dynamic measurements of protein-protein binding or the quantification of kinetic association and dissociation constants of protein interactions. On the other hand, protein binding kinetics quantification can be uniquely done on special expensive surface plasmon resonance (SPR) sensing equipment. Here we report the integration of coupled plasmonic-photonic resonance nanosensors in standard 96-well plate format and by using which, for the very first time, the demonstration of label-free dynamic SPR-like protein binding measurement and kinetics quantification in a generic microplate reader. Our low-cost label-free nanosensor plate enables very sensitive detection of immobilized protein interactions based on the transmission optical density (OD) value changes at specific wavelengths measured in a generic microplate reader. The relative end-point OD value changes show a good linear response with protein concentrations (from 0.05 to 50 μg/ml). And the protein quantification in serum results are consistent with the concurrent hospital lab tests. Most importantly, the kinetic association and dissociation constants of protein interactions in our sensor plate wells are determined by time-lapse dynamic OD value measurement in the generic microplate reader. Enabled by our unique nanosensor plate, SPR-like measurement of protein binding kinetics is now available using generic microplate reader ubiquitous in many chemistry and biomedical research labs.
几乎没有分析检测方法,无论是比色法还是荧光法,能够对通用微孔板读数器进行蛋白质-蛋白质结合的动态测量,或者对蛋白质相互作用的动力学结合和离解常数进行定量。另一方面,蛋白质结合动力学的定量分析只能在特殊的昂贵的表面等离子体共振(SPR)传感设备上进行。在这里,我们报告了耦合等离子体-光子共振纳米传感器在标准 96 孔板格式中的集成,并且首次在通用微孔板读数器中展示了无标记的动态 SPR 样蛋白质结合测量和动力学定量。我们的低成本无标记纳米传感器板能够基于在通用微孔板读数器中测量的特定波长的传输光密度(OD)值变化,非常灵敏地检测固定化蛋白质相互作用。相对终点 OD 值变化与蛋白质浓度呈良好的线性响应(从 0.05 到 50μg/ml)。并且血清中的蛋白质定量结果与同期医院实验室测试结果一致。最重要的是,我们的传感器板孔中的蛋白质相互作用的动力学结合和解离常数是通过在通用微孔板读数器中进行时移动态 OD 值测量来确定的。通过我们独特的纳米传感器板,现在可以使用通用微孔板读数器对蛋白质结合动力学进行类似于 SPR 的测量,这种通用微孔板读数器在许多化学和生物医学研究实验室中都很普遍。