化学
铂金
生物标志物
电化学
纳米技术
组合化学
电极
生物化学
催化作用
物理化学
材料科学
作者
Rui Han,Yang Li,Wenqing Wang,Caifeng Ding,Jason J. Davis,Xiliang Luo
标识
DOI:10.1021/acs.analchem.4c04368
摘要
The real world applications of conventional antifouling biosensors based on gold-thiol (Au-S) interfaces are hampered by the progressive competitive displacement of key functionality by ubiquitous biothiols. To overcome this limitation, we introduce here novel platinum-selenium (Pt-Se) interfaces. Thiol displacement tests, antifouling analyses, and density functional theory calculations confirm markedly improved interfacial stability. This was then leveraged through the application of a seleno-multifunctional peptide platform, tailored to the detection of murine double minute 2, in biological samples. A derived amperometric sensing platform exhibited a notably lower detection limit and more accurate target quantification than that supported by analogous Au-S and Pt-S interfaces. We believe that this work broadens the scope of electrochemical sensor construction and holds significant promise for the development of high-fidelity impactful bioassay platforms.
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