Monitoring human telomere DNA hybridization and G-quadruplex formation using gold nanorods

被引:33
作者
Gou, Xin-Chun [1 ]
Liu, Jun [1 ]
Zhang, Hao-Li [1 ]
机构
[1] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
Biosensor; Telomere DNA; G-quadruplex; Gold nanorods (AuNRs); SINGLE-STRANDED-DNA; OPTICAL-PROPERTIES; PLASMON RESONANCE; NANOPARTICLES; FLUORESCENCE; SCATTERING; ABSORPTION;
D O I
10.1016/j.aca.2010.04.027
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A facile and multi-response strategy for studying the transformations of human telomere DNA from single strand (ss) to double strand (ds) and G-quadruplex has been established by using positively charged gold nanorod (AuNR) as an optical label. The conformation change information of the telomere DNA was transferred into multiple optical signals, including changes in fluorescence emission, near infrared (NIR) absorption, plasma resonance light scattering (PRLS) and dynamic light scattering (DLS) response. The formations of dsDNA and G-quadruplex DNA induced fluorescence quenching of dye on DNA, and were accompanied by the intensity decrease and blue shift of the longitudinal absorption peak of AuNRs. Meanwhile, PRLS and DLS results revealed slightly increased AuNR aggregation due to increased charge density of dsDNA and G-quadruplex DNA as compared to ssDNA. Control experiment suggests that the AuNR-based assay is highly sequence specific; and the high sensitivity allows the study of human telomere DNA at a concentration as low as 58 nM. (c) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:208 / 214
页数:7
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