Gold nanoparticles based molecular beacons for in vitro and in vivo detection of the matriptase expression on tumor

被引:32
作者
Deng, Dawei [1 ]
Zhang, Dongyin [1 ]
Li, Yang [1 ]
Achilefu, Samuel [2 ]
Gu, Yueqing [1 ]
机构
[1] China Pharmaceut Univ, Dept Biomed Engn, Nanjing 210009, Jiangsu, Peoples R China
[2] Washington Univ, Sch Med, Dept Radiol, St Louis, MO 63110 USA
基金
中国国家自然科学基金;
关键词
Molecular beacon; Gold nanoparticle; Matriptase; Peptide substrate; In vitro and in vivo detection; QUANTUM DOTS; PROTEASE; METALLOPROTEINASES; NANOCRYSTALS; TARGET; CANCER; CELLS; SIZE;
D O I
10.1016/j.bios.2013.05.018
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Matriptase, a type II transmembrane serine protease, is responsible for the early stage proliferation of a wide range of human cancers. It is highly expressed on the surface of tumor cells, allowing the protease to serve as a biomarker of cancer detection. Hence, in this study, we designed two molecular beacons consisting of a fluorescent dye-peptide conjugate attached to gold nanoparticles (Au NPs) for in vitro and in vivo detection of the matriptase expression on tumor cells. The peptide substrate (GRQSRAGC) for matriptase served as the linker between dye (donor) and Au NP (acceptor). In this configuration, the dye fluorescence was quenched by Au NP under physiological conditions and recovered after selective cleavage of the GRQSRAGC by matriptase. To maximize spectral overlap between dye fluorescence and Au NP absorption and optimize the quenching efficiency mediated by fluorescence resonance energy transfer (FRET), the visible dye (fluorescein) and near-infrared (NIR) dye peptide conjugates were each attached to spherical and rod-shaped Au NP for in vitro and in vivo detection, respectively. Both in vitro cell and in vivo animal studies indicate that these two molecular beacons are sensitive and specific for the detection of matriptase expression in the tumor, thereby paving the way to image the activities of this diagnostic protease in living organisms. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:216 / 221
页数:6
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