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Yeast Genomics Technique for High-Throughput Drug Target Discovery
被引:1
|作者:
Sun, Zijun
[1
]
Sun, Yanyan
[1
]
Zhou, Yaxian
[1
]
Wan, Yakun
[1
]
机构:
[1] Southeast Univ, Inst Life Sci, Minist Educ, Key Lab Dev Genes & Human Dis, Nanjing 210096, Jiangsu, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Chemical genomic profiling;
target identification;
yeast mutants;
high-throughput;
PROTEIN-PROTEIN INTERACTIONS;
LARGE-SCALE ANALYSIS;
MECHANISM-OF-ACTION;
SACCHAROMYCES-CEREVISIAE;
CANDIDA-ALBICANS;
SCHIZOSACCHAROMYCES-POMBE;
FUNCTIONAL GENOMICS;
3-HYBRID SYSTEM;
WIDE SCREEN;
BIOACTIVE COMPOUNDS;
D O I:
10.1002/ddr.21030
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Preclinical Research The budding yeast Saccharomyces cerevisiae has been a singularly useful eukaryote for the development of Chemical genomic techniques for use in drug discovery studies. Particularly, yeast genomic methodologies provide a solid foundation for high-throughput drug target identification. The success of genomic profiling in budding yeast led to the use of chemical genomics approaches in higher eukaryotic systems. In the present overview, the focus was principally on high-throughput chemical genomic technologies that are advancing the utility of yeast in the drug development research. This led to the review of chemical genomic technologies in other biological systems and the applications of drug synergy in pharmacological research. Finally, the development of genome-wide drug screening was reviewed in the context of drug synergy strategies for discovering novel combinatorial therapies.
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页码:398 / 405
页数:8
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