A liquid crystal-based sensor for the simple and sensitive detection of cellulase and cysteine

被引:24
作者
Wang, Yi [1 ]
Hu, Qiongzheng [2 ]
Tian, Tongtong [1 ,3 ]
Gao, Yan'an [4 ]
Yu, Li [1 ]
机构
[1] Shandong Univ, Minist Educ, Key Lab Colloid & Interface Chem, Jinan 250100, Peoples R China
[2] Univ Houston, Dept Chem, Houston, TX 77204 USA
[3] Qufu Normal Univ, Sch Chem & Chem Engn, Qufu 273165, Peoples R China
[4] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
基金
中国国家自然科学基金;
关键词
Liquid crystals; Sensor; Cellulase; Cysteine; HEAVY-METALS; NANOCLUSTERS; POLYELECTROLYTE; HOMOCYSTEINE; BIOSENSORS; SUBSTRATE; PROTEINS; SURFACES; DROPLETS; PHENOLS;
D O I
10.1016/j.colsurfb.2016.07.059
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A liquid crystal (LC)-based sensor, which is capable of monitoring enzymatic activity at the aqueous/LC interface and detecting cellulase and cysteine (Cys), was herein reported. When functionalized with a surfactant, dodecyl beta-D-glucopyranosicie, the 4-cyano-4'-pentylbiphenyl (5CB) displays a dark-to-bright transition in the optical appearance for cellulase. We attribute this change to the orientational transition of LCs, as a result of enzymatic hydrolysis between cellulase and surfactant. Furthermore, by adding cellulase and Cu2+, our surfactant-LCs system performs an interesting ability to detect Cys, even though Cys could not interact with surfactant or LC directly. Alternatively, through the strong binding between Cys and Cu2+, cellulase was able to hydrolyze surfactant in the presence of Cu2+, leading to the transition of LCs from dark to bright. The detection limit of the LC sensor was around 1 x 10(-5) mg/mL and 82.5 mu M for cellulase and Cys, respectively. The LC-based sensor may contribute to the development of low-cost, expedient, and label-free detection for cellulase and Cys and the design strategy may also provide a novel way for detecting multiple analytes. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:100 / 105
页数:6
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