A label-free optical technique for detecting small molecule interactions

被引:66
作者
Lin, B [1 ]
Qiu, J [1 ]
Gerstenmeier, J [1 ]
Li, P [1 ]
Pien, HM [1 ]
Pepper, J [1 ]
Cunningham, B [1 ]
机构
[1] SRU Biosyst, Woburn, MA 01801 USA
关键词
optical biosensor; small molecule assay; direct assay; high throughput screening; microtiter plate; resonant diffraction;
D O I
10.1016/S0956-5663(02)00077-5
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A novel approach for the label-free detection of molecular interactions is presented in which a colorimetric resonant grating is used as a surface binding platform. The grating, when illuminated with white light, is designed to reflect only a single wavelength. When molecules are attached to the surface, the reflected wavelength (color) is shifted due to the change of the optical path of light that is coupled into the grating. By linking receptor molecules to the grating surface, complementary binding molecules can be detected without the use of any kind of fluorescent probe or radioactive label. The detection technique is capable of detecting the addition and removal of small molecules as they interact with receptor molecules on the sensor surface or enzymes in the solution surrounding the sensor. Two assays are presented to exemplify the detection of small molecule interactions with the biosensor. First, an avidin receptor layer is used to detect 244 Da biotin binding. Second, a protease assay is performed in which a 136 Da p-nitroanilide (pNA) moeity is cleaved from an immobilized substrate. Because the sensor structure can be embedded in the plastic surfaces of microtiter plates or the glass surfaces of microarray slides, it is expected that this technology will be most useful in applications where large numbers of biomolecular interactions are measured in parallel, particularly when molecular labels will alter or inhibit the functionality of the molecules under study. Screening of pharmaceutical compound libraries with protein targets, and microarray screening of protein protein interactions for proteomics are examples of applications that require the sensitivity and throughput afforded by this approach. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:827 / 834
页数:8
相关论文
共 17 条
[1]   Proteomics: applications in basic and applied biology [J].
Anderson, NL ;
Matheson, AD ;
Steiner, S .
CURRENT OPINION IN BIOTECHNOLOGY, 2000, 11 (04) :408-412
[2]   Label-free observation of DNA-hybridisation and endonuclease activity on a wave guide surface using a grating coupler [J].
Bier, FF ;
Scheller, FW .
BIOSENSORS & BIOELECTRONICS, 1996, 11 (6-7) :669-674
[3]   OPTICAL PROBES AND TRANSDUCERS [J].
BRECHT, A ;
GAUGLITZ, G .
BIOSENSORS & BIOELECTRONICS, 1995, 10 (9-10) :923-936
[4]  
CUNNINGHAM A, 1998, BIOANALYTICAL SENSOR, P1
[5]   A plastic colorimetric resonant optical biosensor for multiparallel detection of label-free biochemical interactions [J].
Cunningham, B ;
Lin, B ;
Qiu, J ;
Li, P ;
Pepper, J ;
Hugh, B .
SENSORS AND ACTUATORS B-CHEMICAL, 2002, 85 (03) :219-226
[6]   Colorimetric resonant reflection as a direct biochemical assay technique [J].
Cunningham, B ;
Li, P ;
Lin, B ;
Pepper, J .
SENSORS AND ACTUATORS B-CHEMICAL, 2002, 81 (2-3) :316-328
[7]   Antibody arrays for high-throughput screening of antibody-antigen interactions [J].
de Wildt, RMT ;
Mundy, CR ;
Gorick, BD ;
Tomlinson, IM .
NATURE BIOTECHNOLOGY, 2000, 18 (09) :989-994
[8]   DIRECT OPTICAL IMMUNOSENSING (SENSITIVITY AND SELECTIVITY) [J].
HUBER, W ;
BARNER, R ;
FATTINGER, C ;
HUBSCHER, J ;
KOLLER, H ;
MULLER, F ;
SCHLATTER, D ;
LUKOSZ, W .
SENSORS AND ACTUATORS B-CHEMICAL, 1992, 6 (1-3) :122-126
[9]   Interference-based detection of nucleic acid targets on optically coated silicon [J].
Jenison, R ;
Yang, S ;
Haeberli, A ;
Polisky, B .
NATURE BIOTECHNOLOGY, 2001, 19 (01) :62-65
[10]   A BIOSENSOR CONCEPT BASED ON IMAGING ELLIPSOMETRY FOR VISUALIZATION OF BIOMOLECULAR INTERACTIONS [J].
JIN, G ;
TENGVALL, P ;
LUNDSTROM, I ;
ARWIN, H .
ANALYTICAL BIOCHEMISTRY, 1995, 232 (01) :69-72