Protein Reporter Bioassay Systems for the Phenotypic Screening of Candidate Drugs: A Mouse Platform for Anti-Aging Drug Screening

被引:8
作者
Chiba, Takuya [1 ]
Tsuchiya, Tomoshi [2 ]
Mori, Ryoichi [1 ]
Shimokawa, Isao [1 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Dept Invest Pathol, Nagasaki 8528523, Japan
[2] Nagasaki Univ, Grad Sch Biomed Sci, Div Surg Oncol, Nagasaki 8528501, Japan
来源
SENSORS | 2012年 / 12卷 / 02期
基金
日本科学技术振兴机构;
关键词
drug development; high throughput screening; reporter mice; age-related disorders; GENE ASSAYS; TRANSCRIPTIONAL ACTIVITY; ALKALINE-PHOSPHATASE; EXPRESSION; CELLS; INHIBITORS; DISCOVERY; INDICATOR; RECEPTOR; MICE;
D O I
10.3390/s120201648
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Recent drug discovery efforts have utilized high throughput screening (HTS) of large chemical libraries to identify compounds that modify the activity of discrete molecular targets. The molecular target approach to drug screening is widely used in the pharmaceutical and biotechnology industries, because of the amount of knowledge now available regarding protein structure that has been obtained by computer simulation. The molecular target approach requires that the structure of target molecules, and an understanding of their physiological functions, is known. This approach to drug discovery may, however, limit the identification of novel drugs. As an alternative, the phenotypic- or pathway-screening approach to drug discovery is gaining popularity, particularly in the academic sector. This approach not only provides the opportunity to identify promising drug candidates, but also enables novel information regarding biological pathways to be unveiled. Reporter assays are a powerful tool for the phenotypic screening of compound libraries. Of the various reporter genes that can be used in such assays, those encoding secreted proteins enable the screening of hit molecules in both living cells and animals. Cell-and animal-based screens enable simultaneous evaluation of drug metabolism or toxicity with biological activity. Therefore, drug candidates identified in these screens may have increased biological efficacy and a lower risk of side effects in humans. In this article, we review the reporter bioassay systems available for phenotypic drug discovery.
引用
收藏
页码:1648 / 1656
页数:9
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