A novel fluorescence-based array biosensor:: Principle and application to DNA hybridization assays

被引:16
作者
Schultz, E. [1 ]
Galland, R. [1 ]
Du Boueetiez, D. [1 ]
Flahaut, T. [1 ]
Planat-Chretien, A. [1 ]
Lesbre, F. [2 ]
Hoang, A. [2 ]
Volland, H. [3 ]
Perraut, F. [1 ]
机构
[1] Commissariat Energie Atom, Lab Imagerie & System Acquisit, F-38054 Grenoble, France
[2] Commissariat Energie Atom, Lab Fonctionnalisat Chim Microcomposants, F-38054 Grenoble, France
[3] CEA Saclay, Lab Etudes & Rech & Immuno Anal, F-91191 Gif Sur Yvette, France
关键词
optical biosensor; total internal reflection; real-time detection; surface reaction monitoring;
D O I
10.1016/j.bios.2007.10.006
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A novel fluorescence-based array biosensor targeted for field applications, such as environmental monitoring, has been developed, and successfully applied to DNA hybridization assays. The purpose was to meet the demand for automated, portable but easy-to-maintain systems allowing continuous flow monitoring of surface reactions. The biosensor presented here can be distinguished from the existing systems by the optical method used, which provides an enhanced simplicity and robustness, and enables a simple maintenance by potentially unskilled personnel. The system is based on a conventional microscope slide which acts both as transducer and biological array sensor. The excited fluorescence is guided by total internal reflection into the slide to the detector which is directly interfaced to the slide. Each region of the sensor array is successively optically interrogated, and the detection of the corresponding fluorescent emission synchronized. A real-time three-analyte analysis is thus feasible without any mechanical scanning movement or optical imaging systems as generally used in the existing instruments. The ability of the biosensor to operate in continuous flow for several tens of hours has been demonstrated. The biosensor has been assessed in terms of stability, and slide-to-slide reproducibility, which is found to be less than 3.7%, thus far below the standard biological reproducibility. DNA hybridization assays were performed to estimate a limit of detection, which was found to be 16 mol/mu m(2), and to determine the reaction kinetics associated to the DNA model used. The developed biosensor is thus shown to be able to predict reaction kinetics, and to monitor in real time surface reactions between targets and probes. (C) 2008 Published by Elsevier B.V.
引用
收藏
页码:987 / 994
页数:8
相关论文
共 33 条
[1]   Multi-analyte interrogation using the fiber optic biosensor [J].
Anderson, GP ;
King, KD ;
Gaffney, KL ;
Johnson, LH .
BIOSENSORS & BIOELECTRONICS, 2000, 14 (10-11) :771-777
[2]   Optical chemical and biochemical sensors: new trends [J].
Baldini, F ;
Giannetti, A .
OPTO-IRELAND 2005: OPTICAL SENSING AND SPECTROSCOPY, 2005, 5826 :485-499
[3]  
BERTHIER J, 2004, P 2004 BIOS C GRAN S
[4]  
BRADLEY RA, 1987, PHILOS T R SOC B, V316, P143
[5]   Theoretical analysis of protein concentration determination using biosensor technology under conditions of partial mass transport limitation [J].
Christensen, LLH .
ANALYTICAL BIOCHEMISTRY, 1997, 249 (02) :153-164
[6]  
DANIELS PB, 1998, SPIE, V3259, P28
[7]   AN ASSAY FOR HUMAN CHORIONIC-GONADOTROPIN USING THE CAPILLARY FILL IMMUNOSENSOR [J].
DEACON, JK ;
THOMSON, AM ;
PAGE, AL ;
STOPS, JE ;
ROBERTS, PR ;
WHITELEY, SC ;
ATTRIDGE, JW ;
LOVE, CA ;
ROBINSON, GA ;
DAVIDSON, GP .
BIOSENSORS & BIOELECTRONICS, 1991, 6 (03) :193-199
[8]   Characterizing high-affinity antigen/antibody complexes by kinetic- and equilibrium-based methods [J].
Drake, AW ;
Myszka, DG ;
Klakamp, SL .
ANALYTICAL BIOCHEMISTRY, 2004, 328 (01) :35-43
[9]  
EGGERS M, 1994, BIOTECHNIQUES, V17, P516
[10]   Array Biosensor: Optical and Fluidics Systems [J].
Feldstein, Mark J. ;
Golden, Joel P. ;
Rowe, Chris A. ;
MacCraith, Brian D. ;
Ligler, Frances S. .
BIOMEDICAL MICRODEVICES, 1999, 1 (02) :139-153