A label-free sensing method for phosphopeptides using two-layer gold nanoparticle-based localized surface plasma resonance spectroscopy

被引:13
作者
Chen, Jen-Yi [1 ]
Chen, Yu-Chie [1 ]
机构
[1] Natl Chiao Tung Univ, Dept Appl Chem, Hsinchu 300, Taiwan
关键词
Gold nanoparticles; LSPR; Phosphopeptides; Label-free sensing; TITANIUM-DIOXIDE MICROCOLUMNS; MASS-SPECTROMETRY; BIOMOLECULAR INTERACTIONS; PROTEIN-PHOSPHORYLATION; SELECTIVE ENRICHMENT; FIBRINOPEPTIDE-A; FIBRINOGEN; GLASS; IDENTIFICATION; IMMUNOASSAY;
D O I
10.1007/s00216-010-4397-x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this study, a new type of localized surface plasmon resonance (LSPR) sensing substrate for phosphopeptides was explored. It has been known that LSPR response for target species is larger in the near-infrared region (NIR) than in the visible region of the electromagnetic spectrum. Several types of noble metal nanoparticles (NPs) with NIR absorption capacities have been previously demonstrated as effective LSPR-sensing nanoprobes. Herein, we demonstrate a straightforward approach with improved sensitivity by simply using layer-by-layer (LBL) spherical Au NPs self-assembled on glass slides as the LSPR-sensing substrates that are responsive in the NIR region of the electromagnetic spectrum. The modified glass slide acquired an LSPR absorption band in the NIR, which resulted from the dipole-dipole interactions between Au NPs. To enable the chip to sense phosphopeptides, the surface of the glass chip was spin-coated with thin titania film (TiO2-Glass@Au NPs). Absorption spectrophotometry was employed as a detection tool. Tryptic digest of alpha-casein was used as a model sample. The feasibility of using the new LSPR approach for detecting a potential risk factor leading to cancers (i.e., phosphorylated fibrinopeptide A) directly from human serum samples was demonstrated. Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) was used to confirm the results.
引用
收藏
页码:1173 / 1180
页数:8
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