Anantha Pooja, Raj Piyush, Zheng Peng, Tanwar Swati, Barman Ishan
Department of Mechanical Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.
Department of Oncology, Johns Hopkins University, Baltimore, MD 21287, USA.
Sens Actuators B Chem. 2025 Jan 15;423. doi: 10.1016/j.snb.2024.136811. Epub 2024 Oct 19.
Sensitive detection of disease-specific biomarkers with high accuracy is crucial for early diagnosis, therapeutic monitoring, and understanding underlying pathological mechanisms. Traditional methods, such as immunohistochemistry and enzyme-linked immunosorbent assays (ELISA), face limitations due to the complex and expensive production of antibodies. In this context, aptamers, short oligonucleotides with advantages like easy synthesis, low cost, high specificity, and stability, have emerged as promising alternatives for biomolecular sensing. In this study, we introduce a surface-enhanced Raman spectroscopy (SERS) aptasensor for the multiplexed detection of human α-thrombin and vascular endothelial growth factor (VEGF-165). By leveraging aptamer-based biorecognition elements, our approach capitalizes on the small gaps created by aptamers, generating intense electromagnetic hotspots that significantly amplify the SERS signal. This enables simultaneous detection of human α-thrombin and VEGF-165 with remarkable sensitivity (100 fM and 1 pM, respectively). Notably, we also employ a digital protocol for analyzing the obtained vibrational spectra, marking the first-time utilization of this method for such aptasensors and offering precise quantification even at ultralow concentration regimes. We envision the reported aptasensor aptamer-based spectroscopical tools for a wide range of applications in biology and medicine.
高精度灵敏检测疾病特异性生物标志物对于早期诊断、治疗监测以及理解潜在病理机制至关重要。传统方法,如免疫组织化学和酶联免疫吸附测定(ELISA),由于抗体生产复杂且昂贵而面临局限性。在此背景下,适配体,即具有易于合成、低成本、高特异性和稳定性等优点的短寡核苷酸,已成为生物分子传感的有前途的替代物。在本研究中,我们介绍了一种用于多重检测人α-凝血酶和血管内皮生长因子(VEGF-165)的表面增强拉曼光谱(SERS)适配体传感器。通过利用基于适配体的生物识别元件,我们的方法利用适配体产生的小间隙,产生强烈的电磁热点,显著放大SERS信号。这使得能够同时以显著的灵敏度(分别为100 fM和1 pM)检测人α-凝血酶和VEGF-165。值得注意的是,我们还采用了一种数字协议来分析获得的振动光谱,这标志着该方法首次用于此类适配体传感器,并且即使在超低浓度范围内也能提供精确的定量。我们设想所报道的基于适配体传感器的光谱工具可用于生物学和医学中的广泛应用。