Gold NanoBipyramids Performing as Highly Sensitive Dual-Modal Optical Immunosensors

被引:48
作者
Campu, Andreea [1 ,3 ]
Lerouge, Frederic [2 ]
Chateau, Denis [2 ]
Chaput, Frederic [2 ]
Baldeck, Patrice [2 ]
Parola, Stephane [2 ]
Maniu, Dana [3 ]
Craciun, Ana Maria [1 ]
Vulpoi, Adriana [4 ]
Astilean, Simion [1 ,3 ]
Focsan, Monica [1 ]
机构
[1] Babes Bolyai Univ, Nanobiophoton & Laser Microspect Ctr, Interdisciplinary Res Inst Bionanosci, Treboniu Laurean 42, Cluj Napoca 400271, Romania
[2] Univ Lyon 1, Ecole Normale Super Lyon, CNRS, Lab Chim UMR 5182, 46 Allee Italie, F-69364 Lyon 07, France
[3] Babes Bolyai Univ, Biomol Phys Dept, Fac Phys, M Kogalniceanu 1, Cluj Napoca 400084, Romania
[4] Babes Bolyai Univ, Interdisciplinary Res Inst Bionanosci, Nanostruct Mat & Bionanointerfaces Ctr, Treboniu Laurian 42, Cluj Napoca 400271, Romania
关键词
SURFACE-PLASMON RESONANCE; NANOPARTICLES; SERS; QUANTIFICATION; SPECTROSCOPY; IMMUNOASSAY; ENHANCEMENT; NANORODS; UNIFORM;
D O I
10.1021/acs.analchem.8b01689
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, we demonstrate the feasibility of gold bipyramidal-shaped nanoparticles (AuBPs) to be used as active plasmonic nanoplatforms for the detection of the biotin-streptavidin interaction in aqueous solution via both Localized Surface Plasmon Resonance and Surface Enhanced Raman Scattering (LSPR/SERS). Our proof of concept exploits the precise attachment of the recognition element at the tips of AuBPs, where the electromagnetic field is stronger, which is beneficial to the surface sensitivity of longitudinal LSPR on the local refractive index and to the electromagnetic enhancement of SERS activity, too. Indeed, successive red shifts of the longitudinal LSPR associated with increased local refractive index reveal the attachment of para-aminothiophenol (p-ATP) chemically labeled Biotin to the Au surface and the specific capture of the target protein by biotin-functionalized AuBPs. Finite-Difference Time-Domain simulations based on the reconstructed index of refraction confirm LSPR measurements. However, the molecular identification of the biotin-streptavidin interaction remains elusive by LSPR investigation alone. Remarkably, we succeeded to complement the LSPR detection with reliable SERS measurements which permitted to (a) certify the molecular identification of biotin-streptavidin interaction and (b) extend the limit of detection of streptavidin in solution toward 10(-12) M. Finally, to further probe the possibility to implement the AuBPs as dual LSPR-SERS based immunoassays in solution for real clinical diagnostics, we additionally investigated the AuBP's performance to transduce the specific antihuman IgG- human IgG binding event, providing thus a reference design for building unique plasmonic immunoassays for dual-optical detection of target proteins in aqueous solution.
引用
收藏
页码:8567 / 8575
页数:9
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