Department of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, California 93106, United States.
Center for Bioengineering, University of California Santa Barbara, Santa Barbara, California 93106, United States.
ACS Sens. 2023 Aug 25;8(8):3051-3059. doi: 10.1021/acssensors.3c00632. Epub 2023 Aug 16.
Electrochemical aptamer-based (EAB) sensors are capable of measuring the concentrations of specific molecules in vivo, in real time, and with a few-second time resolution. For their signal transduction mechanism, these sensors utilize a binding-induced conformational change in their target-recognizing, redox-reporter-modified aptamer to alter the rate of electron transfer between the reporter and the supporting electrode. While a variety of voltammetric techniques have been used to monitor this change in kinetics, they suffer from various drawbacks, including time resolution limited to several seconds and sensor-to-sensor variation that requires calibration to remove. Here, however, we show that the use of fast Fourier transform electrochemical impedance spectroscopy (FFT-EIS) to interrogate EAB sensors leads to improved (here better than 2 s) time resolution and calibration-free operation, even when such sensors are deployed in vivo. To showcase these benefits, we demonstrate the approach's ability to perform real-time molecular measurements in the veins of living rats.
基于电化学适体的(EAB)传感器能够实时测量体内特定分子的浓度,具有几秒钟的时间分辨率。对于它们的信号转导机制,这些传感器利用其目标识别的结合诱导构象变化,氧化还原报告修饰适体来改变报告分子和支持电极之间的电子转移速率。虽然已经使用了各种伏安技术来监测这种动力学变化,但它们存在各种缺点,包括时间分辨率限于几秒钟,以及传感器之间的差异需要校准才能消除。然而,在这里,我们表明,使用快速傅里叶变换电化学阻抗谱(FFT-EIS)来询问 EAB 传感器可以提高(这里优于 2 秒)时间分辨率和免校准操作,即使这些传感器在体内使用也是如此。为了展示这些优势,我们展示了该方法在活体大鼠静脉中进行实时分子测量的能力。