Fabrication of a bioconjugated dual-functional SERS probe for facile compound screening and detection

化学 X射线光电子能谱 质谱法 拉曼光谱 表面等离子共振 分子 纳米团簇 基质(水族馆) 纳米技术 纳米颗粒 材料科学 色谱法 有机化学 化学工程 物理 地质学 工程类 光学 海洋学
作者
Dandan Zhang,Junhong Ma,Xinxin Zheng,Zilong Zhang,Xiaojuan Lian,Xue Zhao,Xinfeng Zhao
出处
期刊:Biosensors and Bioelectronics [Elsevier]
卷期号:234: 115369-115369 被引量:1
标识
DOI:10.1016/j.bios.2023.115369
摘要

Surface-enhanced Raman spectroscopy (SERS) is an ultrasensitive technique for both detection and structural characterizations. To further exploit these advantages, we designed and fabricated a dual-functional SERS probe for specific capture and fast detection of small molecule ligands binding to target protein from a mixture of compounds such as extracts of natural products. As a proof of concept, we synthesized SiO2@Ag nanoclusters that are coated with 6-chlorohexanoic acid for covalent immobilization of serotonin transporter (5-HTT) fused with a Halo-tag through enzyme-substrate recognition. As such, we fabricated a bioconjugated SERS probe, and the synthesis, coating, protein immobilization, and affinity-based ligand binding have been characterized and verified by transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS), and elemental mapping. By applying this probe to analyze Gardenia jasminoides extract, we have successfully identified crocin I as a compound binding to 5-HTT, which was further proved by using mass spectrometry (MS) and nuclear magnetic resonance (NMR). Taken together, we have developed a novel SERS probe by integrating the inherent strength of SERS in molecular analysis with an extended functionality of affinity-guided molecular capture, which has demonstrated the potential in drug screening of challenging systems.
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