An Unconventional Immunosensor for Biomolecule Detection via Nonspecific Gold Nanoparticle–Antibody Interactions

化学 生物分子 胶体金 分析物 纳米颗粒 石英晶体微天平 基质(水族馆) 纳米技术 检出限 免疫金标记 组合化学 抗体 色谱法 生物物理学 生物化学 吸附 有机化学 材料科学 免疫学 生物 海洋学 地质学
作者
Song Chen,Siqi Ji,Hongwei Sun,Yu Lei,Jing Zhao
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:96 (19): 7367-7372 被引量:1
标识
DOI:10.1021/acs.analchem.4c00598
摘要

Immunogold, that is, gold nanoparticles (AuNPs) conjugated with biomolecules such as antibodies and peptides, have been widely used to construct sandwiched immunosensors for biodetection. Two main challenges in these immunoassays are difficulties in finding and validating a suitable antibody, and the nonspecific interaction between the substrate and immunogold, which lowers the detection sensitivity and even causes false results. To avoid these issues, we took advantage of the nonspecific interaction between AuNPs and capture antibodies and proposed a new sensing mechanism. That is, after the capture of analyte targets by the capture antibodies on the substrate, AuNPs of certain chemical functionality would preferably bind to the free capture antibodies. Consequently, the amount of deposited AuNPs will inversely depend on the concentration of the analytes. As a proof-of-concept, we designed a mass-based sensor where anti-IgG antibodies were coated on a quartz crystal microbalance substrate. After IgG was introduced, tannic acid-capped AuNPs were applied to bind with the free anti-IgG antibody molecules. A frequency change (Δf) of the quartz substrate was induced by the increased mass loading. To further amplify the loading mass, an Ag enhancer solution was added, and Ag growth was catalyzed by the bound AuNPs. The Δf response showed a concentration-dependent decrease when increasing IgG concentration with a detection limit of 2.6 ng/mL. This method relies on the nonspecific interaction between AuNPs and anti-IgG antibodies to realize sensitive detection of IgG and eliminates the use of detection antibodies. The concept is an alternative to many existing immunoassay technologies.
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