DNA Origami Directed Au Nanostar Dimers for Single-Molecule Surface-Enhanced Raman Scattering

被引:151
作者
Tanwar, Swati [1 ]
Haldar, Krishna Kanta [2 ]
Sen, Tapasi [1 ]
机构
[1] Inst Nano Sci & Technol, Phase 10,Sect 64, Mohali 160062, Punjab, India
[2] Cent Univ Punjab, Dept Chem Sci, Sch Basic & Appl Sci, Bathinda 151001, Punjab, India
关键词
GOLD NANOSTARS; ENERGY-TRANSFER; NANOPARTICLE; SERS; FLUORESCENCE; SPECTROSCOPY; OPTIMIZATION; NANOANTENNAS; SIZE; SENSITIVITY;
D O I
10.1021/jacs.7b10410
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We demonstrate the synthesis of Au nanostar dimers with tunable interparticle gap and controlled stoichiometry assembled on DNA origami. Au nanostars with uniform and sharp tips were immobilized on rectangular DNA origami dimerized structures to create nanoantennas containing monomeric and dimeric Au nanostars. Single Texas red (TR) dye was specifically attached in the junction of the dimerized origami to act as a Raman reporter molecule. The SERS enhancement factors of single TR dye molecules located in the conjunction region in dimer structures having interparticle gaps of 7 and 13 nm are 2 X 10(10) and 8 X 10(9), respectively, which are strong enough for single analyte detection. The highly enhanced electromagnetic field generated by the plasmon coupling between sharp tips and cores of two Au nanostars in the wide conjunction region allows the accommodation and specific detection of large biomolecules. Such DNA directed assembled nanoantennas with controlled interparticle separation distance and stoichiometry, and well-defined geometry, can be used as excellent substrates in single-molecule SERS spectroscopy and will have potential applications as a reproducible platform in single-molecule sensing.
引用
收藏
页码:17639 / 17648
页数:10
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