A modular, fully integrated ultra-high-throughput screening system based on confocal fluorescence analysis techniques

被引:22
作者
Jäger, S
Garbow, N
Kirsch, A
Preckel, H
Gandenberger, FU
Herrenknecht, K
Rüdiger, M
Hutchinson, JP
Bingham, RP
Ramon, F
Bardera, A
Martin, J
机构
[1] Evotec OAI, Evotec Technol, D-22525 Hamburg, Germany
[2] GlaxoSmithKline, Harlow, Essex, England
[3] GlaxoSmithKline, Madrid, Spain
关键词
integrated screening system; high-throughput screening; fluorescence; single molecule detection; confocal optics; homogenous assay; cellular assay; cell imaging;
D O I
10.1177/1087057103258475
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The rapid increase in size of compound libraries, as well as new targets emerging from the Human Genome Project, require progress in ultra-high-throughput screening (uHTS) systems. In a joint effort with scientists and engineers from the biotech and the pharmaceutical industry, a modular, fully integrated system for miniaturized uHTS was developed. The goal was to achieve high data quality in small assay volumes (1-4 muL) combined with reliable and unattended operation. Two new confocal fluorescence readers have been designed. One of the instruments is a 4-channel confocal fluorescence reader, measuring with 4 objectives in parallel. The fluorescence readout is based on single-molecule detection methods, allowing high sensitivity at low tracer concentrations and delivering an information-rich output. The other instrument is a confocal fluorescence imaging reader, where the images are analyzed in terms of generic patterns and quantified in units of intensity per pixel. Both readers are spanning the application range from assays with isolated targets in homogenous solution or membrane vesicle-based assays (4-channel reader) to cell-based assays (imaging reader). Results from a comprehensive test on these assay types demonstrate the high quality and robustness of this screening system.
引用
收藏
页码:648 / 659
页数:12
相关论文
共 21 条
[1]   Fluorescence correlation spectroscopy: lead discovery by miniaturized HTS [J].
Auer, M ;
Moore, KJ ;
Meyer-Almes, FJ ;
Guenther, R ;
Pope, AJ ;
Stoeckli, KA .
DRUG DISCOVERY TODAY, 1998, 3 (10) :457-465
[2]   The photon counting histogram in fluorescence fluctuation spectroscopy [J].
Chen, Y ;
Müller, JD ;
So, PTC ;
Gratton, E .
BIOPHYSICAL JOURNAL, 1999, 77 (01) :553-567
[3]   Highly sensitive fluorescence detection technology currently available for HTS [J].
Eggeling, C ;
Brand, L ;
Ullmann, D ;
Jäger, S .
DRUG DISCOVERY TODAY, 2003, 8 (14) :632-641
[4]   Monitoring conformational dynamics of a single molecule by selective fluorescence spectroscopy [J].
Eggeling, C ;
Fries, JR ;
Brand, L ;
Günther, R ;
Seidel, CAM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) :1556-1561
[5]   A dileucine motif in the C terminus of the beta(2)-adrenergic receptor is involved in receptor internalization [J].
Gabilondo, AM ;
Hegler, J ;
Krasel, C ;
BoivinJahns, V ;
Hein, L ;
Lohse, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (23) :12285-12290
[6]   Single-molecule detection technologies in miniaturized high-throughput screening:: Fluorescence intensity distribution analysis [J].
Haupts, U ;
Rüdiger, M ;
Ashman, S ;
Turconi, S ;
Bingham, R ;
Wharton, C ;
Hutchinson, J ;
Carey, C ;
Moore, KJ ;
Pope, AJ .
JOURNAL OF BIOMOLECULAR SCREENING, 2003, 8 (01) :19-33
[7]   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
[8]   Two-dimensional fluorescence intensity distribution analysis:: Theory and applications [J].
Kask, P ;
Palo, K ;
Fay, N ;
Brand, L ;
Mets, Ü ;
Ullmann, D ;
Jungmann, J ;
Pschorr, J ;
Gall, K .
BIOPHYSICAL JOURNAL, 2000, 78 (04) :1703-1713
[9]  
Kino G. S., 1995, HDB BIOL CONFOCAL MI
[10]   Ligand binding to transmembrane receptors on intact cells or membrane vesicles measured in a homogeneous 1-microliter assay format [J].
Klumpp, M ;
Scheel, A ;
Lopez-Calle, E ;
Busch, M ;
Murray, KJ ;
Pope, AJ .
JOURNAL OF BIOMOLECULAR SCREENING, 2001, 6 (03) :159-170