Wang Bei, Xu Yang, Li Han, Song Zishuo, Guan Tian, He Yonghong
Shenzhen Key Laboratory for Minimal Invasive Medical Technologies, Institute of Optical Imaging and Sensing, Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.
Institute of Biopharmaceutical and Health Engineering, Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.
Biosensors (Basel). 2025 Apr 23;15(5):268. doi: 10.3390/bios15050268.
Biomolecule detection is pivotal in disease diagnosis. In this study, we present a novel aptamer-antibody sandwich module integrated with an imaging weak measurement system to enhance the sensitivity and specificity of biomolecule detection. The feasibility of this approach is demonstrated using CA125. CA125 is a glycoprotein tumor marker widely used for ovarian cancer diagnosis and monitoring, with its level changes closely associated with disease progression. Given its clinical significance, developing highly sensitive and specific CA125 detection methods is crucial for precision medicine. The dual-recognition mechanism combines the high affinity of aptamers and the specificity of antibodies, significantly improving detection performance while utilizing antibodies for signal amplification. In the presence of CA125, the anti-CA125 aptamer immobilized on the chip surface captures the target, which is then specifically bound by the CA125 antibody, forming the aptamer-CA125-antibody complex. This interaction induces a change in the refractive index of the chip surface, which is detected by the imaging weak measurement system and ultimately manifested as a variation in light intensity in the resulting images. The method achieves the highly sensitive detection of CA125 in the 0.01 mU/mL range to 100 U/mL, with preliminary results showing a detection resolution of 3.98 μU/mL and high specificity against non-target proteins. Additionally, detecting CA125 in serum samples further validates the feasibility of the method's applicability in complex biological matrices. The proposed method offers significant advantages, including high sensitivity, high specificity, label-free, multiplexed detection, low cost, and real-time detection, making it a promising platform for bio-molecule detection with a wide range of applications.
生物分子检测在疾病诊断中至关重要。在本研究中,我们提出了一种新型的适配体 - 抗体夹心模块,其与成像弱测量系统集成,以提高生物分子检测的灵敏度和特异性。使用CA125证明了该方法的可行性。CA125是一种糖蛋白肿瘤标志物,广泛用于卵巢癌的诊断和监测,其水平变化与疾病进展密切相关。鉴于其临床意义,开发高灵敏度和特异性的CA125检测方法对于精准医学至关重要。双重识别机制结合了适配体的高亲和力和抗体的特异性,在利用抗体进行信号放大的同时显著提高了检测性能。在存在CA125的情况下,固定在芯片表面的抗CA125适配体捕获靶标,然后该靶标被CA125抗体特异性结合,形成适配体 - CA125 - 抗体复合物。这种相互作用引起芯片表面折射率的变化,该变化由成像弱测量系统检测,并最终表现为所得图像中光强度的变化。该方法实现了在0.01 mU/mL至100 U/mL范围内对CA125的高灵敏度检测,初步结果显示检测分辨率为3.98 μU/mL,并且对非靶标蛋白具有高特异性。此外,在血清样本中检测CA125进一步验证了该方法在复杂生物基质中应用的可行性。所提出的方法具有显著优势,包括高灵敏度、高特异性、无标记、多重检测、低成本和实时检测,使其成为一种具有广泛应用前景的生物分子检测平台。