Streamlining the Drug Discovery Process by Integrating Miniaturization, High Throughput Screening, High Content Screening, and Automation on the CellChip™ System

被引:61
作者
Kapur, Ravi [1 ]
Giuliano, Kenneth A. [1 ]
Campana, Martha [1 ]
Adams, Terri [1 ]
Olson, Keith [1 ]
Jung, David [1 ]
Mrksich, Milan [2 ]
Vasudevan, Chandrasekaran [1 ]
Taylor, D. Lansing [1 ]
机构
[1] Cellomics Inc, Pittsburgh, PA 15237 USA
[2] Univ Chicago, Dept Chem, Chicago, IL 60637 USA
关键词
drug discovery; CellChip; high content screening; fluorescence; patterning; sensors; microarrays; bioinformatics; tissue engineering;
D O I
10.1023/A:1009993519771
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A major bottleneck to the early stages of drug discovery is the absence of integration of high throughput screening (HTS) with smarter assays that screen "hits'' from HTS to identify leads (High content screening, HCS). We propose a solution using novel fluorescent engineered protein biosensors integrated into a miniaturized live-cell-based screening platform (CellChip (TM) System) that markedly shortens the early drug discovery process. Microarrays of selectively localized living cells, containing engineered fluorescent biosensors, serve to integrate HTS and HCS onto a single platform. HTS "hits'' are identified using one biosensor while reading the whole chip array of cells. The high-biological content information is then obtained from probing target activity at inter-cellular, sub-cellular and molecular levels in the "hit'' wells. HCS assays yield temporal-spatial dynamic maps of the drug-target interaction within each living cell. We predict that a new platform incorporating HTS and HCS assays that are automated, miniaturized, and information-rich will dramatically improve the decision making process in the pharmaceutical industry and optimize lead compounds during the early part of the drug discovery process. There is an opportunity to establish a new paradigm for drug discovery based on integration of fluorescence technology, micropatterning of living cells, automated optical detection and data analysis, and a new generation of knowledge building bioinformatics approaches. The technology will have an expansive impact spanning the fields of drug discovery, biomedical research, environmental monitoring, life sciences, and clinical diagnostics. The integrated CellChip (TM) Platform with miniaturized tissue-specific microarrayed cells capable of providing inter-cellular and sub-cellular spatio-temporal information in response to drug-cell, toxin-cell, or pathogen-cell interactions will serve to enhance the decision making process in drug discovery, toxicology, and clinical diagnostics.
引用
收藏
页码:99 / 109
页数:11
相关论文
共 16 条
[1]  
[Anonymous], 1998, HIGH THROUGHPUT SCRE
[2]   Macrophages and heat shock proteins [J].
Bachelet, M ;
Adrie, C ;
Polla, BS .
RESEARCH IN IMMUNOLOGY, 1998, 149 (7-8) :727-732
[3]   I-KAPPA-B - A SPECIFIC INHIBITOR OF THE NF-KAPPA-B TRANSCRIPTION FACTOR [J].
BAEUERLE, PA ;
BALTIMORE, D .
SCIENCE, 1988, 242 (4878) :540-546
[4]   TUMOR-NECROSIS-FACTOR AND INTERLEUKIN-1 LEAD TO PHOSPHORYLATION AND LOSS OF I-KAPPA-B-ALPHA - A MECHANISM FOR NF-KAPPA-B ACTIVATION [J].
BEG, AA ;
FINCO, TS ;
NANTERMET, PV ;
BALDWIN, AS .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (06) :3301-3310
[5]   Quantification of G-protein coupled receptor internalization using G-protein coupled receptor-green fluorescent protein conjugates with the ArrayScan™ high-content screening system [J].
Conway, BR ;
Minor, LK ;
Xu, JZ ;
Gunnet, JW ;
DeBiasio, R ;
D'Andrea, MR ;
Rubin, R ;
DeBiasio, R ;
Giuliano, K ;
Zhou, LB ;
Demarest, KT .
JOURNAL OF BIOMOLECULAR SCREENING, 1999, 4 (02) :75-86
[6]   Characterization and quantitation of NF-κB nuclear translocation induced by interleukin-1 and tumor necrosis factor-α -: Development and use of a high capacity fluorescence cytometric system [J].
Ding, GJF ;
Fischer, PA ;
Boltz, RC ;
Schmidt, JA ;
Colaianne, JJ ;
Gough, A ;
Rubin, RA ;
Miller, DK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (44) :28897-28905
[7]   High-content screening: A new approach to easing key bottlenecks in the drug discovery process [J].
Giuliano, KA ;
DeBiasio, RL ;
Dunlay, RT ;
Gough, A ;
Volosky, JM ;
Zock, J ;
Pavlakis, GN ;
Taylor, DL .
JOURNAL OF BIOMOLECULAR SCREENING, 1997, 2 (04) :249-259
[8]   Fluorescent-protein biosensors: new tools for drug discovery [J].
Giuliano, KA ;
Taylor, DL .
TRENDS IN BIOTECHNOLOGY, 1998, 16 (03) :135-140
[9]  
GIULIANO KA, 1995, ANNU REV BIOPH BIOM, V24, P405, DOI 10.1146/annurev.bb.24.060195.002201
[10]  
Kapur R., 1999, GOMAC P