Shenzhen Key Laboratory for Minimal Invasive Medical Technologies, Institute of Optical Imaging and Sensing, Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.
School of Medicine, Tsinghua University, Beijing 100084, China.
Biosensors (Basel). 2024 Jul 8;14(7):332. doi: 10.3390/bios14070332.
The demand for accurate and efficient immunoassays calls for the development of precise, high-throughput analysis methods. This paper introduces a novel approach utilizing a weak measurement interface sensor for immunoassays, offering a solution for high throughput analysis. Weak measurement is a precise quantum measurement method that amplifies the weak value of a system in the weak interaction through appropriate pre- and post-selection states. To facilitate the simultaneous analysis of multiple samples, we have developed a chip with six flow channels capable of conducting six immunoassays concurrently. We can perform real-time immunoassay to determine the binding characteristics of spike protein and antibody through real-time analysis of the flow channel images and calculating the relative intensity. The proposed method boasts a simple structure, eliminating the need for intricate nano processes. The spike protein concentration and relative intensity curve were fitted using the Log-Log fitting regression equation, and R was 0.91. Utilizing a pre-transformation approach to account for slight variations in detection sensitivity across different flow channels, the present method achieves an impressive limit of detection(LOD) of 0.85 ng/mL for the SARS-CoV-2 the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein, with a system standard deviation of 5.61. Furthermore, this method has been successfully verified for monitoring molecular-specific binding processes and differentiating binding capacities.
对准确、高效免疫分析的需求促使人们开发精确、高通量的分析方法。本文提出了一种利用弱测量界面传感器进行免疫分析的新方法,为高通量分析提供了一种解决方案。弱测量是一种精确的量子测量方法,通过适当的预和后选择态来放大系统在弱相互作用中的弱值。为了便于同时分析多个样本,我们开发了一种具有六个流道的芯片,能够同时进行六个免疫分析。我们可以通过实时分析流道图像并计算相对强度来进行实时免疫分析,以确定刺突蛋白和抗体的结合特性。该方法结构简单,无需复杂的纳米工艺。利用对数-对数拟合回归方程拟合了刺突蛋白浓度和相对强度曲线,R 值为 0.91。利用预变换方法来考虑不同流道之间检测灵敏度的微小变化,本方法实现了对 SARS-CoV-2 刺突蛋白的检测限(LOD)低至 0.85ng/mL,系统标准偏差为 5.61。此外,该方法已成功验证可用于监测分子特异性结合过程和区分结合能力。