Amorim Rodrigo G, Lima Filipe C D A, Leão de Souza Fábio Arthur, Scopel Wanderlã L, Prasongkit Jariyanee, Scheicher Ralph H
Departamento de Física, ICEx, Universidade Federal Fluminense - UFF, Volta Redonda, RJ, Brazil.
Federal Institute of Education, Science and Techonology of São Paulo, Matão, SP, Brazil.
Nanoscale. 2025 Jan 29;17(5):2498-2505. doi: 10.1039/d4nr03359k.
Amino acids are fundamental building blocks of proteins, playing critical roles in medical diagnostics, environmental monitoring, and biomarker identification. The development of nanoscale electronic sensors capable of single-amino-acid recognition has gained significant attention due to their potential for label-free, real-time detection. In this study, we investigate the electronic transport properties of amino acids in two gold-based nanodevices with distinct architectures: a gold nanojunction and a gold-capacitor system. Using density functional theory (DFT) in combination with nonequilibrium Green's function (NEGF) calculations, we explore the sensing mechanism and conductance variations induced by different amino acids, including select phosphorylated variants. Each device was assigned a reference amino acid, F (M), for a capacitor (nanojunction) to differentiate its conductance from other molecules. Our results reveal distinct conductance that enables amino acid classification based on their electronic signatures, demonstrating that molecular discrimination is primarily governed by conductance variations as a function of the binding energy differences. The nanojunction exhibited remarkable differentiation for the amino acids S, pS, Y, and pY, rendering it especially proficient in distinguishing between structurally analogous molecules. These findings highlight the strong potential of gold-based nanodevices for precise amino acid detection, paving the way for advancements in biosensing technologies, molecular diagnostics, and biomedical applications.
氨基酸是蛋白质的基本组成部分,在医学诊断、环境监测和生物标志物识别中发挥着关键作用。能够识别单个氨基酸的纳米级电子传感器的开发因其无标记、实时检测的潜力而备受关注。在本研究中,我们研究了两种具有不同结构的金基纳米器件中氨基酸的电子传输特性:金纳米结和金电容器系统。结合密度泛函理论(DFT)和非平衡格林函数(NEGF)计算,我们探索了不同氨基酸(包括选定的磷酸化变体)引起的传感机制和电导变化。为每个器件指定了一种参考氨基酸,对于电容器(纳米结)为F(M),以区分其与其他分子的电导。我们的结果揭示了不同的电导,能够根据氨基酸的电子特征对其进行分类,表明分子识别主要由作为结合能差异函数的电导变化决定。纳米结对氨基酸S、pS、Y和pY表现出显著的区分能力,使其特别擅长区分结构相似的分子。这些发现突出了金基纳米器件在精确氨基酸检测方面的强大潜力,为生物传感技术、分子诊断和生物医学应用的进步铺平了道路。