Surface plasmon resonance imaging on a microchip for detection of DNA-modified gold nanoparticles deposited onto the surface in a non-cross-linking configuration

被引:47
作者
Sato, Yasunobu [1 ]
Sato, Kae [1 ]
Hosokawa, Kazuo [1 ]
Maeda, Mizuo [1 ]
机构
[1] RIKEN, Bioengn Lab, Wako, Saitama 3510198, Japan
关键词
SNP typing; surface plasmon resonance imaging; gold nanoparticles; microchip;
D O I
10.1016/j.ab.2006.04.035
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recently we reported that gold nanoparticles (GNPs) with fully matched duplexes on their surfaces are selectively deposited onto walls of poly(dimethylsiloxane) (PDMS) microchannels at high salt concentrations. In this study, the surface plasmon resonance (SPR) imaging technique was applied to monitor this phenomenon for improvement of detection sensitivity and elucidation of the phenomenon. The microchip was fabricated by bonding a surface-patterned PDMS plate and a gold thin film-deposited glass substrate. Probe oligonucleotide-modified GNPs were hybridized with target oligonucleotides to make fully matched or single-base-mismatched duplexes. The hybridized GNP solution was mixed with an NaCl solution in a Y-shaped microchannel. The deposition of the GNPs onto the gold sensor surface was detected by SPR imaging. Discrimination of the targets was possible with limit of detection of 32 nM (19 fmol) without temperature control in 5 min. Detailed analysis indicated that a seed layer of GNPs was initially adsorbed onto the sensor surface regardless of the target sequence. Therefore, in combination with a portable SPR device, the proposed method is promising for point-of-care testing of single-nucleotide polymorphsims. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:125 / 131
页数:7
相关论文
共 33 条
[21]  
Nataraj AJ, 1999, ELECTROPHORESIS, V20, P1177, DOI 10.1002/(SICI)1522-2683(19990101)20:6<1177::AID-ELPS1177>3.0.CO
[22]  
2-2
[23]   Nanostructures in biodiagnostics [J].
Rosi, NL ;
Mirkin, CA .
CHEMICAL REVIEWS, 2005, 105 (04) :1547-1562
[24]   A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms [J].
Sachidanandam, R ;
Weissman, D ;
Schmidt, SC ;
Kakol, JM ;
Stein, LD ;
Marth, G ;
Sherry, S ;
Mullikin, JC ;
Mortimore, BJ ;
Willey, DL ;
Hunt, SE ;
Cole, CG ;
Coggill, PC ;
Rice, CM ;
Ning, ZM ;
Rogers, J ;
Bentley, DR ;
Kwok, PY ;
Mardis, ER ;
Yeh, RT ;
Schultz, B ;
Cook, L ;
Davenport, R ;
Dante, M ;
Fulton, L ;
Hillier, L ;
Waterston, RH ;
McPherson, JD ;
Gilman, B ;
Schaffner, S ;
Van Etten, WJ ;
Reich, D ;
Higgins, J ;
Daly, MJ ;
Blumenstiel, B ;
Baldwin, J ;
Stange-Thomann, NS ;
Zody, MC ;
Linton, L ;
Lander, ES ;
Altshuler, D .
NATURE, 2001, 409 (6822) :928-933
[25]   Non-cross-linking gold nanoparticle aggregation as a detection method for single-base substitutions [J].
Sato, K ;
Hosokawa, K ;
Maeda, M .
NUCLEIC ACIDS RESEARCH, 2005, 33 (01) :e4
[26]   Rapid aggregation of gold nanoparticles induced by non-cross-linking DNA hybridization [J].
Sato, K ;
Hosokawa, K ;
Maeda, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (27) :8102-8103
[27]   Use of surface plasmon resonance to probe the equilibrium and dynamic aspects of interactions between biological macromolecules [J].
Schuck, P .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 1997, 26 :541-566
[28]   Diagnosis of HNF-1α mutations on a PNA zip-code microarray by single base extension -: art. no. e19 [J].
Song, JY ;
Park, HG ;
Jung, SO ;
Park, J .
NUCLEIC ACIDS RESEARCH, 2005, 33 (02) :e19
[29]   SNP discovery in associating genetic variation with human disease phenotypes [J].
Suh, Y ;
Vijg, J .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2005, 573 (1-2) :41-53
[30]   Accessing genetic variation:: Genotyping single nucleotide polymorphisms [J].
Syvänen, AC .
NATURE REVIEWS GENETICS, 2001, 2 (12) :930-942