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

被引:0
|
作者
Zhang, Xiaonan [1 ,2 ]
Zhang, Lizhong [1 ]
Li, Han [1 ]
Xu, Yang [1 ]
Meng, Lingqin [1 ]
Liang, Gengyu [1 ]
Wang, Bei [1 ]
Liu, Le [3 ]
Guan, Tian [1 ,2 ]
Guo, Cuixia [4 ]
He, Yonghong [1 ,5 ]
机构
[1] Tsinghua Univ, Inst Opt Imaging & Sensing, Shenzhen Int Grad Sch, Shenzhen Key Lab Minimal Invas Med Technol, Shenzhen 518055, Peoples R China
[2] Tsinghua Univ, Sch Med, Beijing 100084, Peoples R China
[3] Tsinghua Univ, Inst Mat Res, Shenzhen Int Grad Sch, Shenzhen 518055, Peoples R China
[4] Fuzhou Univ, Sch Mech Engn & Automat, Fuzhou 350108, Peoples R China
[5] Tsinghua Univ, Jilin Fuyuan Guan Food Grp Joint Res Ctr, Shenzhen Int Grad Sch, Shenzhen 518055, Peoples R China
来源
BIOSENSORS-BASEL | 2024年 / 14卷 / 07期
基金
中国国家自然科学基金;
关键词
weak measurement; high throughput immunoassay; optical biosensor; SARS-CoV-2 spike protein; LABEL-FREE; ANTIBODIES; BINDING;
D O I
10.3390/bios14070332
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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.
引用
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页数:12
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