New Insights into Surface-Enhanced Raman Spectroscopy Label-Free Detection of DNA on Ag°/TiO2 Substrate

被引:17
作者
He, Lijie [1 ,2 ]
Langlet, Michel [1 ,2 ]
Bouvier, Pierre [1 ,2 ]
Calers, Christophe [1 ,2 ,3 ,4 ]
Pradier, Claire-Marie [1 ,2 ,3 ,4 ]
Stambouli, Valerie [1 ,2 ]
机构
[1] Univ Grenoble Alpes, LMGP, F-38000 Grenoble, France
[2] CNRS, LMGP, F-38000 Grenoble, France
[3] Univ Paris 06, Sorbonne Univ, Lab React Surface, F-75005 Paris, France
[4] CNRS, UMR 7197, Lab React Surface, F-75005 Paris, France
关键词
FUNCTIONAL THEORETICAL DFT; NUCLEIC-ACID BASES; ADENINE ADSORPTION; SCATTERING; SERS; SILVER; SPECTRA; CONSTITUENTS; AG; DERIVATIVES;
D O I
10.1021/jp507462y
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Four DNA polybases (polyA, polyC, polyG, and polyT), modified or not with an external NH2 group, have been immobilized on an original, robust, and low-cost Ag degrees/TiO2 surface-enhanced Raman spectroscopy (SERS) platform. The latter was elaborated through an optimized chemically assisted photocatalytic reduction process. The label-free SERS detection of these polybases has been performed, and the analysis of SERS spectra has been supported by X-ray photoelectron spectroscopy measurements. The high-resolution and signal/noise ratio of SERS spectra enabled us to clearly index the main and secondary Raman lines of all types of studied polybases and to propose some aspects of the polybase immobilization mechanism. Regardless of polybase type and presence or absence of NH2 modification, an optimum detection is obtained for polybase concentrations lying in the 510 mu M range, which gives rise to reproducible SERS spectra. This behavior has been interpreted in terms of distribution, orientation, and packing density of immobilized molecules.
引用
收藏
页码:25658 / 25670
页数:13
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