药物发现
计算生物学
蛋白质组学
酿酒酵母
芽殖酵母
酵母
鉴定(生物学)
基因组学
化学基因学
功能基因组学
药物开发
生物
药物靶点
生物信息学
药品
遗传学
基因组
生物化学
小分子
基因
药理学
植物
作者
Ainslie B. Parsons,Ron Geyer,Timothy R. Hughes,Charles Boone
出处
期刊:PubMed
日期:2003-01-01
卷期号:5: 159-66
被引量:28
摘要
Small, cell permeable, and target-specific chemical ligands are highly valuable, not only as therapeutics but also as research tools. The synthesis, identification and characterization of these compounds is often a difficult task. The straightforward genetics of the budding yeast Saccharomyces cerevisiae, and the high degree of conservation of basic cellular processes between yeast and higher organisms makes yeast an excellent tool for drug development studies, particularly in regards to anticancer and anti-fungal drug discovery. Recent advances in yeast functional genomics and proteomics studies are changing the field of yeast research. Many of these new technologies are readily applicable to drug target identification and other aspects of drug discovery. This review will focus on current genetic, genomic, and proteomic methodologies in S. cerevisiae that have the potential to be useful in drug discovery and target validation.
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