Center for Molecular Recognition Selectivity and Biosensing, School of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China.
Shanghai Key Laboratory of Bio-Energy Crop, School of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China.
Mikrochim Acta. 2020 May 13;187(6):327. doi: 10.1007/s00604-020-04289-5.
Extension of the self-assembled bionanonetworks into surface plasmon resonance (SPR) assay investigation provides an effective signal amplification approach. We fabricated a bionetwork by nucleic acids, organic compounds, and supramolecular gold nanoparticles for ultrasensitive SPR detection of B-type natriuretic peptide (BNP). The SPR method was developed by a sandwich-type format of aptamer-target-antibody, and the aptamer-modified bionanonetworks induced localized SPR and large refractive index for different concentrations of the target BNP. The linear concentration range and limit of detection were 1-10,000 pg/mL (R = 0.9852) and 0.3 pg/mL respectively. The detection recovery was in the range 92.13 to 108.69%. The approach embraces the following main advantages: (1) Cooperative double recognition was realized by calix[4]arenes for amino aptamers and pyridinium porphyrins. (2) The approach provided the specificity for supramolecular-based nanomaterials and a simple synthesis process via the ordered self-assembly under mild conditions. (3) The bionanonetworks endowed the SPR assay with signal amplification and stable determination for trace proteins. Therefore, it is expected that this study may offer a new SPR signal-amplified platform of organic-inorganic bionanonetworks to achieve sensitive, stable, and real-time determination. Graphical abstract Schematic of bionanonetwork based on porphyrin-mediated functionalized gold nanoparticles for SPR signal amplification to quantitatively detect BNP.
将自组装的生物纳米网络扩展到表面等离子体共振(SPR)分析中,提供了一种有效的信号放大方法。我们通过核酸、有机化合物和超分子金纳米粒子制造了生物网络,用于超灵敏 SPR 检测 B 型利钠肽(BNP)。SPR 方法采用适体-靶标-抗体的三明治型格式,适体修饰的生物纳米网络诱导局部 SPR 和不同浓度靶标 BNP 的大折射率。线性浓度范围和检测限分别为 1-10,000 pg/mL(R=0.9852)和 0.3 pg/mL。检测回收率在 92.13%至 108.69%之间。该方法具有以下主要优点:(1)杯[4]芳烃实现了对氨基适体和吡啶卟啉的协同双重识别。(2)该方法通过温和条件下的有序自组装提供了基于超分子的纳米材料的特异性和简单的合成过程。(3)生物纳米网络为 SPR 分析提供了信号放大和痕量蛋白质的稳定测定。因此,预计本研究可为基于有机-无机生物纳米网络的 SPR 信号放大平台提供新的途径,以实现灵敏、稳定和实时的测定。