Tanwar, SwatiHaldar, Krishna KantaSen, TapasiTanwar, S.Haldar, K.K.Sen, T.2018-02-012024-08-132018-02-012024-08-132017Tanwar, S., Haldar, K. K., & Sen, T. (2017). DNA Origami Directed Au Nanostar Dimers for Single-Molecule Surface-Enhanced Raman Scattering. Journal of the American Chemical Society, 139(48), 17639-17648. doi: 10.1021/jacs.7b104102786310.1021/jacs.7b10410http://10.2.3.109/handle/32116/561We 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 ? 1010 and 8 ? 109, 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. ? 2017 American Chemical Society.enArticlehttps://pubs.acs.org/doi/10.1021/jacs.7b10410