BioSensor Technologies, AIT-Austrian Institute of Technology GmbH, Muthgasse 11, 1190 Vienna, Austria.
Analyst. 2017 Oct 9;142(20):3913-3921. doi: 10.1039/c7an00469a.
The sensitive analysis of small lipid extracellular vesicles (EVs) by using a grating-coupled surface plasmon resonance (GC-SPR) biosensor has been reported. In order to enable the analysis of trace amounts of EVs present in complex liquid samples, the target analyte is pre-concentrated on the sensor surface by using magnetic nanoparticles and its affinity binding is probed by wavelength interrogation of SPR. The GC-SPR has been demonstrated to allow for the implementation of efficient pulling of EVs to the sensor surface by using magnetic nanoparticles and an external magnetic field gradient applied through the sensor chip. This approach overcomes slow diffusion-limited mass transfer and greatly enhances the measured sensor response. The specific detection of different EV populations secreted from mesenchymal stem cells is achieved with a SPR sensor chip modified with antibodies against the surface marker CD81 and magnetic nanoparticles binding the vesicles via annexin V and cholera toxin B chain.
已报道了使用光栅耦合表面等离子体共振(GC-SPR)生物传感器对小脂质细胞外囊泡(EVs)进行灵敏分析。为了能够分析复杂液体样品中存在的痕量 EVs,目标分析物通过磁性纳米粒子在传感器表面上进行预浓缩,并通过 SPR 的波长检测来探测其亲和结合。GC-SPR 已被证明可以通过使用磁性纳米粒子和通过传感器芯片施加的外部磁场梯度将 EVs 有效地拉到传感器表面。这种方法克服了缓慢的扩散限制的质量传递,并大大增强了测量的传感器响应。通过用针对表面标记物 CD81 的抗体修饰 SPR 传感器芯片,并通过膜联蛋白 V 和霍乱毒素 B 链结合囊泡的磁性纳米粒子,实现了对间充质干细胞分泌的不同 EV 群体的特异性检测。