Amplified electrochemical detection of surface biomarker in breast cancer stem cell using self-assembled supramolecular nanocomposites

被引:44
作者
Zhao, Jing [1 ,2 ]
Tang, Yingying [1 ]
Cao, Ya [1 ]
Chen, Tianshu [1 ]
Chen, Xiaoxia [1 ]
Mao, Xiaoxia [1 ,2 ]
Yin, Yongmei [3 ]
Chen, Guifang [1 ,2 ]
机构
[1] Shanghai Univ, Sch Life Sci, Ctr Mol Recognit & Biosensing, Shanghai 200444, Peoples R China
[2] Shanghai Univ, Sch Commun & Informat Engn, Inst Biomed Engn, Shanghai 200444, Peoples R China
[3] Nanjing Med Univ, Dept Oncol, Affiliated Hosp 1, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
CD44; Supramolecular chemistry; Breast cancer stem cell; Signal amplification; Electrochemical technique; CIRCULATING TUMOR-CELLS; SENSITIVE DETECTION; IDENTIFICATION; RECOGNITION; COMPLEX; CD44; HYALURONAN; PLATFORM; PROTEIN; ASSAY;
D O I
10.1016/j.electacta.2018.07.002
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Cancer stem cells (CSCs) are recognized as an important source of cancers. Surface biomarkers play a critical role for CSCs profiling and also for diagnostic purposes. In this paper, we propose self-assembled supramolecular nanocomposites assisted multiple signal amplification strategy, and successfully apply it in electrochemical detection of an important CSCs biomarker CD44 as well as identification of breast CSCs. A supermolecular composite, consisting of a binding peptide that is able to bind to the target CD44 and a self-assembled diphenylalanine (FF) nanostructure that provides a template for deposition of gold nanoparticles (AuNPs), is elaborately constructed on the surface of an electrode through the linkage of cucurbit[8]urils. In the presence of CD44, this supramolecule is able to provide amplified electrochemical signals from silver-enhancement on AuNPs after target-protection from trypsin-catalyzed digestion. Whereas in the absence of the target, this supramolecular architecture is destroyed, resulting in suppressed signals. Linear sweep voltammetry results present a satisfactory specificity and sensitivity, which also demonstrate a wide linear range with a limit of detection of 2.17 pg/mL toward CD44 protein and a limit of detection of 8cells/mL toward CD44-positive cancer cells. Therefore, this work provides a promising prospective for further clinic application in the future. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1072 / 1078
页数:7
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