Graduate School of Life Sciences, Toyo University, Itakura, Gunma 374-0193, Japan.
Faculty of Life Sciences, Toyo University, Itakura, Gunma 374-0193, Japan.
Molecules. 2020 May 8;25(9):2223. doi: 10.3390/molecules25092223.
We describe a patterned surface-enhanced Raman spectroscopy (SERS) substrate with the ability to pre-concentrate target molecules. A surface-adsorbed nanosphere monolayer can serve two different functions. First, it can be made into a SERS platform when covered by silver. Alternatively, it can be fashioned into a superhydrophobic surface when coated with a hydrophobic molecular species such as decyltrimethoxy silane (DCTMS). Thus, if silver is patterned onto a latter type of substrate, a SERS spot surrounded by a superhydrophobic surface can be prepared. When an aqueous sample is placed on it and allowed to dry, target molecules in the sample become pre-concentrated. We demonstrate the utility of the patterned SERS substrate by evaluating the effects of inhibitors to acetylcholinesterase (AChE). AChE is a popular target for drugs and pesticides because it plays a critical role in nerve signal transduction. We monitored the enzymatic activity of AChE through the SERS spectrum of thiocholine (TC), the end product from acetylthiocholine (ATC). Inhibitory effects of paraoxon and carbaryl on AChE were evaluated from the TC peak intensity. We show that the patterned SERS substrate can reduce both the necessary volumes and concentrations of the enzyme and substrate by a few orders of magnitude in comparison to a non-patterned SERS substrate and the conventional colorimetric method.
我们描述了一种具有预浓缩目标分子能力的图案化表面增强拉曼光谱(SERS)基底。表面吸附的纳米球单层可以发挥两种不同的功能。首先,当被银覆盖时,它可以用作 SERS 平台。或者,当用疏水分子物种(例如癸基三甲氧基硅烷(DCTMS))涂覆时,它可以变成超疏水表面。因此,如果将银图案化到后一种类型的基底上,则可以制备出被超疏水表面包围的 SERS 点。当将含有目标分子的水溶液置于其上并使其干燥时,样品中的目标分子会被预浓缩。我们通过评估乙酰胆碱酯酶(AChE)抑制剂的效果来证明图案化 SERS 基底的实用性。AChE 是药物和农药的热门靶标,因为它在神经信号转导中起着至关重要的作用。我们通过硫代胆碱(TC)的 SERS 光谱监测 AChE 的酶活性,TC 是乙酰硫代胆碱(ATC)的终产物。我们从 TC 峰强度评估了对氧磷和carbaryl 对 AChE 的抑制作用。我们表明,与非图案化 SERS 基底和常规比色法相比,图案化 SERS 基底可以将酶和底物的所需体积和浓度降低几个数量级。