Fluorescent quantum dot-labeled aptamer bioprobes specifically targeting mouse liver cancer cells

被引:42
作者
Zhang, Jing [1 ]
Jia, Xing [1 ]
Lv, Xiao-Jing [1 ]
Deng, Yu-Lin [1 ]
Xie, Hai-Yan [1 ]
机构
[1] Beijing Inst Technol, Sch Life Sci, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
Quantum dot; Aptamer; Probe; Label; Cell; CONJUGATED NANOPARTICLES; IN-VIVO; COLLECTION; MOLECULES; NANORODS; DELIVERY; THERAPY; BINDING; LIGANDS;
D O I
10.1016/j.talanta.2009.12.031
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Fluorophore-labeled bioprobes are the key for fluorescent-labeled imaging technology. In the present work, mouse liver hepatoma cell line BNL 1ME A.7R.1 (MEAR)-specific ssDNA aptamer TLS9a was used to fabricate quantum dot-labeled aptamer bioprobe (QD-Apt), which was obtained by conjugating streptavidin-modified quantum dots (SA-QDs) with biotin-derived aptamer via the interaction between biotin and streptavidin. The QD-Apt was of monodispersity and excellent fluorescence properties. When the optimum ratio of SA-QDs to aptamer, which is 1:16, was used in the preparation of the QD-Apt, the resultant QD-Apt was of satisfactory bioactivity. They could specifically recognize MEAR cells and could not recognize BNL cells and Hela cells. Particularly, the growth and viability of QD-Apt bound MEAR cells were not affected by QD-Apt within 84 h compared to control cells, indicating that the probe was biocompatible and suitable for live cell imaging. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:505 / 509
页数:5
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