A novel and robust homogeneous fluorescence-based assay using nanoparticles for pharmaceutical screening and diagnostics

被引:25
作者
Schaertl, S
Meyer-Almes, FJ
Lopez-Calle, E
Siemers, A
Krämer, J
机构
[1] EVOTEC Analyt Syst GMBH, D-40699 Erkrath, Germany
[2] EVOTEC BioSyst AG, D-22525 Hamburg, Germany
关键词
D O I
10.1177/108705710000500405
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have established a new type of homogeneous immunoassay based on nanoparticles (nanoparticle immunoassay, or NPIA) being analyzed using fluorescence intensity distribution analysis (FIDA), This method allows the characterization of single fluorescently labeled molecules or particles with respect to their molecular brightness and concentration, Upon binding of conjugates to molecules coupled to the nanoparticle surface, the brightness of the complex scales with the number of bound conjugates, The complexes can then be distinguished accurately from free conjugate and concentrations of free and bound molecules can be determined reliably. In this study we present various examples of NPIAs where capture antibodies were linked to the nanoparticles, which were either artificial beads or bacteria. Two assay formats have been developed; first, direct labeling of the conjugate was used to quantitate free antigen through competition experiments, and second, an antigen-directed antibody was labeled to establish an assay similar to a sandwich ELISA setup. The major advantages of a NPIA are the robustness and high signal-to-noise ratio at short measurement times, as demonstrated with a miniaturized experiment in a Nanocarrier(TM) holding a volume of 1 mu l/well. in addition to the good data quality, NPIAs are straightforward to perform because they require no washing steps. NPIAs open new dimensions for high throughput pharmaceutical screening and diagnostics. Assay development times can be reduced significantly because of a simple toolbox principle that is applicable to most types of assays.
引用
收藏
页码:227 / 237
页数:11
相关论文
共 16 条
[1]  
AUER M, 1998, INT J IMMUNOPHARMACO, V21, P457
[2]   Minimizing a binding domain from protein A [J].
Braisted, AC ;
Wells, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (12) :5688-5692
[3]   The photon counting histogram in fluorescence fluctuation spectroscopy [J].
Chen, Y ;
Müller, JD ;
So, PTC ;
Gratton, E .
BIOPHYSICAL JOURNAL, 1999, 77 (01) :553-567
[4]  
ELISH ME, 1988, J GEN MICROBIOL, V134, P1355
[5]   Fluorescence-intensity distribution analysis and its application in biomolecular detection technology [J].
Kask, P ;
Palo, K ;
Ullmann, D ;
Gall, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) :13756-13761
[6]   EXTRACELLULAR TRANSPORT OF CHOLERA-TOXIN B-SUBUNIT USING NEISSERIA IGA PROTEASE BETA-DOMAIN - CONFORMATION-DEPENDENT OUTER-MEMBRANE TRANSLOCATION [J].
KLAUSER, T ;
POHLNER, J ;
MEYER, TF .
EMBO JOURNAL, 1990, 9 (06) :1991-1999
[7]   Rapid assay processing by integration of dual-color fluorescence cross-correlation spectroscopy: High throughput screening for enzyme activity [J].
Koltermann, A ;
Kettling, U ;
Bieschke, J ;
Winkler, T ;
Eigen, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) :1421-1426
[8]  
MEYERALMES FJ, 2000, IN PRESS FLUORESCENC
[9]   Single molecule detection technologies in miniaturized high throughput screening: Fluorescence correlation spectroscopy [J].
Moore, KJ ;
Turconi, S ;
Ashman, S ;
Ruediger, M ;
Haupts, U ;
Emerick, V ;
Pope, AJ .
JOURNAL OF BIOMOLECULAR SCREENING, 1999, 4 (06) :335-353
[10]   Homogeneous fluorescence readouts for miniaturized high-throughput screening: theory and practice [J].
Pope, AJ ;
Haupts, UM ;
Moore, KJ .
DRUG DISCOVERY TODAY, 1999, 4 (08) :350-362