纳米技术
沸石咪唑盐骨架
咪唑酯
材料科学
纳米探针
纳米颗粒
等离子体子
吸附
纳米生物技术
化学
纳米传感器
生物传感器
制作
结合
超短脉冲
胶体金
纳米晶
分子
胶体
药物输送
副镜
自组装
化学工程
生物物理学
检出限
选择性
拉曼光谱
荧光
碎片结晶区
纳米尺度
免疫球蛋白Fab片段
纳米机器人学
作者
Jincheng Xiong,Jiangjiang Zhang,Xingyu Jiang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-07-03
卷期号:20 (27): 19256-19271
被引量:1
标识
DOI:10.1021/acsnano.6c02029
摘要
Gold-nanoparticles-based lateral flow immunoassays (AuNPs-LFIAs) are widely used for point-of-care testing, yet their sensitivity remains fundamentally limited, likely because random antibody orientation on AuNP surfaces restricts Fab accessibility and antigen recognition efficiency. Precise control of antibody orientation is thus critical for maximizing probe activity, yet existing directional conjugation strategies are often multistep, technically complex, and poorly scalable. Here, we report an ultrafast biomimetic mineralization strategy that enables one-step, room-temperature self-assembly of zeolitic imidazolate framework-8 (ZIF-8) with antibodies and dual-ligand AuNPs, producing uniform hybrid nanoprobes within 5 min. ZIF-8 shell preserves the plasmonic properties of AuNPs while simultaneously enhancing colloidal stability and optical signal intensity. Molecular dynamics simulations suggest a two-step orientation model: (i) rapid electrostatic attraction between negatively charged Fc regions and Zn 2+ ions initiates nucleation, followed by (ii) Fc-associated interfacial interactions that promote preferential Fc-oriented binding and anisotropic Fc/Fab distribution, thereby enhancing Fab exposure for efficient antigen recognition. This controlled assembly increases Fab accessibility more than 3-fold relative to conventional adsorption or co-precipitation strategies, minimizes nonspecific adsorption, and amplifies signal output. When applied to competitive LFIAs, the oriented nanoprobes enabled ultrasensitive detection of chloramphenicol down to 13 pg/mL, corresponding to approximately 1 order of magnitude higher sensitivity than AuNPs-based LFIA gold standard. By integrating mechanistic insight with operational simplicity, this work establishes a generalizable platform for ultrafast, scalable, and antibody-orientation-controlled nanoprobe fabrication for next-generation LFIAs in food safety, clinical diagnostics, and environmental monitoring.
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