Localized Surface Plasmon Resonance (LSPR) Biosensor for the Protein Detection

被引:0
|
作者
Maximilien Cottat
Néné Thioune
Ana-Maria Gabudean
Nathalie Lidgi-Guigui
Monica Focsan
Simion Astilean
Marc Lamy de la Chapelle
机构
[1] Université Paris 13,Nanobiophotonics and Laser Microspectroscopy Center, Interdisciplinary Research Institute on Bio
[2] Sorbonne Paris Cité,Nano
[3] Laboratoire CSPBAT,Sciences
[4] CNRS (UMR 7244),undefined
[5] Faculty of Physics,undefined
[6] Babes-Bolyai University,undefined
来源
Plasmonics | 2013年 / 8卷
关键词
Localize surface plasmon resonance (LSPR); Gold nanorods (GNRs); Biosensor; Protein;
D O I
暂无
中图分类号
学科分类号
摘要
In this paper, we investigate the ability of the gold nanorods (GNRs) to detect some proteins and demonstrate their potential to be used as plasmonic nanobiosensors. The GNRs were synthesized by a two-step seed-mediated growth procedure at room temperature. Firstly, a seed solution of gold nanoparticles was synthesized in the presence of cetyltrimethylammonium bromide surfactant and, subsequently, incorporated with appropriate amount of silver nitrate and tetrachloroauric acid solutions to grow GNRs with average length of 50 nm and diameter of 14 nm. We study the interaction of GNRs with proteins whose molecular weight varies from 6.5 up to 75 kDa. We investigate the resulting solutions by means of UV–vis absorption spectroscopy to determine the effect of the proteins characteristics on the shift of the localized surface plasmon resonance (LSPR). We show that for the case when proteins are in large excess compared to the GNRs concentration, whatever the protein is, the LSPR shift is constant and does not depend on the protein molecular weight. Moreover, we have been able to demonstrate that the sensitivity of such LSPR sensor is around 10–9 M/nm on a concentration range from 10–10 to 10–8 M. Some comparison with finite-difference time-domain simulations have also shown that the number of proteins adsorbed at the GNRs surface is around 40.
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页码:699 / 704
页数:5
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