Weak Value Amplification Based Optical Sensor for High Throughput Real-Time Immunoassay of SARS-CoV-2 Spike Protein

Biosensors Pub Date : 2024-07-08 DOI:10.3390/bios14070332
Xiaonan Zhang, Lizhong Zhang, Han Li, Yang Xu, Lingqin Meng, Gengyu Liang, Bei Wang, Le Liu, Tian Guan, Cuixia Guo, Yonghong He
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Abstract

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 R2 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.
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基于弱值放大的光学传感器用于 SARS-CoV-2 Spike 蛋白的高通量实时免疫测定
对精确、高效免疫测定的需求要求开发精确、高通量的分析方法。本文介绍了一种利用弱测量界面传感器进行免疫测定的新方法,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,通过适当的前置和后置选择态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品,我们开发了一种具有六个流道的芯片,能够同时进行六种免疫测定。我们可以进行实时免疫测定,通过实时分析流道图像和计算相对强度来确定尖峰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。利用对数拟合回归方程拟合了尖峰蛋白浓度和相对强度曲线,R2 为 0.91。本方法采用预转化方法来考虑不同流道检测灵敏度的微小差异,对严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)尖峰蛋白的检测限(LOD)达到了令人印象深刻的 0.85 纳克/毫升,系统标准偏差为 5.61。此外,该方法在监测分子特异性结合过程和区分结合能力方面也得到了成功验证。
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