Near-infrared excited surface-enhanced Raman scattering of biological molecules on gold colloid I: Effects of pH of the solutions of amino acids and of their polymerization

被引:50
作者
Dou, XM [1 ]
Jung, YM
Yamamoto, H
Doi, S
Ozaki, Y
机构
[1] Shanghai Jiao Tong Univ, Inst Opt & Photon, Shanghai 200030, Peoples R China
[2] KDK Corp, Basic Technol Res Lab, Minami Ku, Kyoto 6018045, Japan
[3] Kwansei Gakuin Univ, Sch Sci, Dept Chem, Nishinomiya, Hyogo 6628501, Japan
关键词
surface-enhanced Raman scattering SERS; near-infrared; amino acid; gold colloid; Raman spectroscopy;
D O I
10.1366/0003702991946406
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Near-infrared (NIR) excited surface-enhanced Raman scattering (SERS) has been measured for lysine (Lys) on gold colloid at pH 10.8 and 12.0 where its epsilon-amino group is ionized and both the alpha- and epsilon-amino groups are neutralized, respectively, The intensities of SERS signals from Lys are much stronger at pH 10.8 than at pH 12.0. This result suggests that the electrostatic interaction between the positive charge of the epsilon-NH3+ group and the negative charge of the gold surface is one of the most important factors which determine the intensities of the SERS signals. A similar SERS study has been carried out for glycine (Gly) on gold colloid at various pH. The SERS spectra of Gly on gold colloid are quite different in terms of both the frequencies and the band intensities from those of Gly on silver colloid, previously reported; the zwitter ion is dominant on the surface of the gold colloid, while the anion form is major on the silver colloid surface. The chemical interactions are much less important for the emergence of SERS of Gly on the gold colloid, NIR SERS has also been performed for oligomers and polymers of Lys and Gly. The intensities of the SERS signals decrease markedly with their polymerization. The effects of the steric hindrance due to the polymerization and of the distance between the gold surface and amino acid unit probably determine the SERS intensities.
引用
收藏
页码:133 / 138
页数:6
相关论文
共 35 条
[1]  
BANDEKAR J, 1982, SPECTROCHIM ACTA A A, V39, P375
[2]  
Chang R.K., 1982, Surface Enhanced Raman Scattering
[3]   SURFACE-ENHANCED RAMAN-SPECTROSCOPY OF BIOMOLECULES .1. WATER-SOLUBLE PROTEINS, DIPEPTIDES AND AMINO-ACIDS [J].
CHUMANOV, GD ;
EFREMOV, RG ;
NABIEV, IR .
JOURNAL OF RAMAN SPECTROSCOPY, 1990, 21 (01) :43-48
[4]  
COTTON TM, 1985, SURFACE INTERFACIAL, V2, P161
[5]  
COTTON TM, 1988, SPECTROSCOPY SURFACE, P91
[6]   PLASMA RESONANCE ENHANCEMENT OF RAMAN-SCATTERING BY PYRIDINE ADSORBED ON SILVER OR GOLD SOL PARTICLES OF SIZE COMPARABLE TO THE EXCITATION WAVELENGTH [J].
CREIGHTON, JA ;
BLATCHFORD, CG ;
ALBRECHT, MG .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1979, 75 :790-798
[7]   CONFORMATION AND ORIENTATION OF THE HAPTENS, 2,4-DINITROPHENYL AMINO-ACIDS, ON COLLOIDAL SILVER FROM SURFACE-ENHANCED RAMAN-SCATTERING [J].
CURLEY, D ;
SIIMAN, O .
LANGMUIR, 1988, 4 (04) :1021-1032
[8]   Enzyme immunoassay utilizing surface-enhanced Raman scattering of the enzyme reaction product [J].
Dou, X ;
Takama, T ;
Yamaguchi, Y ;
Yamamoto, H ;
Ozaki, Y .
ANALYTICAL CHEMISTRY, 1997, 69 (08) :1492-1495
[9]   Quantitative analysis of double-stranded DNA amplified by a polymerase chain reaction employing surface-enhanced Raman spectroscopy [J].
Dou, X ;
Takama, T ;
Yamaguchi, Y ;
Hirai, K ;
Yamamoto, H ;
Doi, S ;
Ozaki, Y .
APPLIED OPTICS, 1998, 37 (04) :759-763
[10]  
DOU X, IN PRESS J RAMAN SPE