Sogol Asaei, Geeta Verma, Nicholas S. Sinclair, Julie N. Renner
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引用次数: 0
摘要
由于对稀土元素(REEs)的需求日益增长,轻松检测稀土元素(REEs)的重要性也随之增加。为了满足这一需求,我们提出了一种创新的电化学生物传感器,并将铈作为稀土元素的模型。这种生物传感器采用了改进的 EF 手环肽序列,其中半胱氨酸用于与金工作电极共价连接,酪氨酸则作为电化学活性氨基酸。传感器的设计原理是,与铈结合后,肽的构象会发生变化,影响酪氨酸与电极表面的接近程度,从而调节电流。根据人工尿液中 0 至 67 μM 的铈浓度,在 ~0.55-0.65 V 处相对于银伪参比电极的循环伏安电流峰值生成了校准曲线。该传感器的生物相关检测限为 35 μM,灵敏度为 -0.0024 ± 0.002 (μA μM)-1。这些发现为设计用于电化学生物传感的肽序列提供了启示。
Electrochemical biosensing of cerium with a tyrosine-functionalized EF-hand loop peptide
The significance of easily detecting rare earth elements (REEs) has increased due to the growing demand for REEs. Addressing this need, we present an innovative electrochemical biosensor, focusing on cerium as a model REE. This biosensor utilizes a modified EF-hand loop peptide sequence, incorporating cysteine for covalent attachment to a gold working electrode and tyrosine as an electrochemically active amino acid. The sensor was designed such that binding to cerium induces a conformational change in the peptide, affecting tyrosine's proximity to the electrode surface, modulating the current. A calibration curve was generated from cyclic voltammetry current peaks at ~0.55–0.65 V versus a silver pseudo-reference electrode, with cerium concentrations ranging from 0 to 67 μM in artificial urine. The sensor exhibited a biologically relevant limit of detection of 35 μM and a sensitivity of −0.0024 ± 0.002 (μA μM)−1. These findings offer insights into designing peptide sequences for electrochemical biosensing.
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