Laser-Activated Gene Silencing via Gold Nanoshell-siRNA Conjugates

被引:215
|
作者
Braun, Gary B. [1 ]
Pallaoro, Alessia [1 ]
Wu, Guohui [2 ,3 ]
Missirlis, Dimitris [2 ,3 ]
Zasadzinski, Joseph A. [2 ,3 ]
Tirrell, Matthew [2 ,3 ]
Reich, Norbert O. [1 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Mat Res Lab, Santa Barbara, CA 93106 USA
关键词
nanoparticle; nanoshell; TAT; laser; gold; silencing; RNA; CELLULAR UPTAKE; TAT PEPTIDE; NANOPARTICLES; CELLS; DELIVERY; RNAI; LOCALIZATION; TRANSFECTION; TEMPERATURE; ABSORPTION;
D O I
10.1021/nn900469q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The temporal and spatial control over the delivery of materials such as siRNA into cells remains a significant technical challenge. We demonstrate the pulsed near-infrared (NIR) laser-dependent release of siRNA from coated 40 nm gold nanoshells. Tat-lipid coating mediates the cellular uptake of the nanomaterial at picomolar concentration, while spatiotemporal silencing of a reporter gene (green fluorescence protein) was studied using photomasking. The NIR laser-induced release of siRNA from the nanoshells is found to be power-and time-dependent, through surface-linker bond cleavage, while the escape of the siRNA from endosomes occurs above a critical pulse energy attributed to local heating and cavitation. NIR laser-controlled drug release from functional nanomaterials should facilitate more sophisticated developmental biology and therapeutic studies.
引用
收藏
页码:2007 / 2015
页数:9
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