生物污染
化学
适体
生物传感器
检出限
结垢
肽
纳米技术
线性范围
组合化学
色谱法
膜
生物化学
材料科学
分子生物学
生物
作者
Min Chen,Rui Han,Wenqi Wang,Yang Li,Xiliang Luo
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2021-09-27
卷期号:93 (40): 13555-13563
被引量:69
标识
DOI:10.1021/acs.analchem.1c02552
摘要
A brief and universal ultralow fouling sensing platform capable of assaying targets in complex biofluids was developed based on designed antifouling peptides that could form a loop-closed structure with enhanced stability. The newly designed peptide with thiol groups in its two terminals self-assembled onto a gold nanoparticle (AuNP)-modified electrode surface to form a stable loop structure, which displayed excellent antifouling performance, outstanding stability under enzymatic hydrolysis, and satisfactory long-term antifouling capability in complex biofluids (clinical human serum). The antifouling and highly sensitive electrochemical aptasensor was constructed via one-step co-immobilization of the designed peptides and aptamers onto the electrode surface modified with electrodeposited poly(3,4-ethylenedioxythiophene) (PEDOT) and AuNPs. The developed peptide-based aptasensor exhibited a decent response for the analysis of the cancer antigen 125 (CA125), with a relatively wide linear range (0.1–1000 U mL–1) and a low limit of detection (0.027 U mL–1), and was capable of detecting CA125 in clinical serum samples with acceptable accuracy. This antifouling strategy-based self-assembled peptide with a loop-closed structure provided a potential path for the development of various low-fouling biosensors for application in complex biological fluids.
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