Author
Listed:
- Nicholas I. Smith
(Biophotonics Laboratory, Immunology Frontier Research Center, Osaka University
PRESTO, Japan Science and Technology Agency (JST))
- Kentaro Mochizuki
(Osaka University)
- Hirohiko Niioka
(Osaka University)
- Satoshi Ichikawa
(Institute for NanoScience Design, Osaka University)
- Nicolas Pavillon
(Biophotonics Laboratory, Immunology Frontier Research Center, Osaka University)
- Alison J. Hobro
(Biophotonics Laboratory, Immunology Frontier Research Center, Osaka University)
- Jun Ando
(Osaka University)
- Katsumasa Fujita
(Osaka University)
- Yutaro Kumagai
(Host Defense Laboratory, Immunology Frontier Research Center, Osaka University)
Abstract
Nanoparticle manipulation is of increasing interest, since they can report single molecule-level measurements of the cellular environment. Until now, however, intracellular nanoparticle locations have been essentially uncontrollable. Here we show that by infusing a gold ion solution, focused laser light-induced photoreduction allows in situ fabrication of gold nanoparticles at precise locations. The resulting particles are pure gold nanocrystals, distributed throughout the laser focus at sizes ranging from 2 to 20 nm, and remain in place even after removing the gold solution. We demonstrate the spatial control by scanning a laser beam to write characters in gold inside a cell. Plasmonically enhanced molecular signals could be detected from nanoparticles, allowing their use as nano-chemical probes at targeted locations inside the cell, with intracellular molecular feedback. Such light-based control of the intracellular particle generation reaction also offers avenues for in situ plasmonic device creation in organic targets, and may eventually link optical and electron microscopy.
Suggested Citation
Nicholas I. Smith & Kentaro Mochizuki & Hirohiko Niioka & Satoshi Ichikawa & Nicolas Pavillon & Alison J. Hobro & Jun Ando & Katsumasa Fujita & Yutaro Kumagai, 2014.
"Laser-targeted photofabrication of gold nanoparticles inside cells,"
Nature Communications, Nature, vol. 5(1), pages 1-9, December.
Handle:
RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms6144
DOI: 10.1038/ncomms6144
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