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The Adaptive BioCD: Interferometric Immunoassay on a Spinning Disk

机译:自适应BioCD:旋转磁盘上的干涉免疫分析

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The speed of interferometric detection is at least 1000 times faster than the fluorometric detection used in the vast majority of clinical diagnostic systems. This opens the possibility to perform thousands of assays in the time it takes fluorescence to perform only one. Molecules immobilized on a spinning disk, like a CD, present the fastest and simplest means of interrogating thousands of micron-scale interferometer elements per second. However, the challenge of interferometry on a spinning disk is to maintain stable phase in the presence of mechanical vibration. In this paper, we demonstrate the first use of adaptive optics in an adaptive optical homodyne mixer to perform interferometry on a multi-analyte BioCD. The BioCD is a 4,, diameter glass disk printed with a spoke pattern of protein. When the disk spins, the periodic protein pattern is transferred into a high-speed optical phase modulation by spinning the disk at 3000 rpm in the path of a probe laser. A nonlinear optical film mixes the signal beam with a stable reference beam in a two-wave mixing configuration that adaptively phase-locks the two beams to create stable phase in spite of mechanical vibration. Specific binding of antibody to printed antigen is detected as an increased homodyne signal. Multi-analyte detection on Anti Mouse and Anti Rabbit IgG is performed in which Mouse IgG and Rabbit IgG act as the non-specific reagent to each other. Detection is made on circular tracks. The technique has the potential of fast screening for large numbers of protein interactions.
机译:干涉检测的速度比绝大多数临床诊断系统中使用的荧光检测至少快1000倍。这开辟了在仅荧光检测一次即可进行数千次检测的可能性。固定在旋转盘(例如CD)上的分子是每秒询问数千个微米级干涉仪元件的最快,最简单的方法。然而,旋转盘上的干涉测量法的挑战是在存在机械振动的情况下保持稳定的相位。在本文中,我们演示了在自适应光学零差混频器中首次使用自适应光学器件对多分析物BioCD进行干涉测量。 BioCD是一个直径为4的玻璃盘,上面印有蛋白质的辐条图案。当磁盘旋转时,通过在探测激光的路径中以3000 rpm的速度旋转磁盘,周期性的蛋白质图案将转换为高速光学相位调制。非线性光学膜以两波混合配置将信号光束与稳定的参考光束混合,该混合光束尽管存在机械振动,也可以自适应地锁相两束光束以产生稳定的相位。检测到抗体与印刷抗原的特异性结合,作为增加的零差信号。进行抗小鼠和抗兔IgG的多分析物检测,其中小鼠IgG和兔IgG相互充当非特异性试剂。在圆形轨道上进行检测。该技术具有快速筛选大量蛋白质相互作用的潜力。

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