酵母基因组学和蛋白质组学在药物发现和靶标验证中的应用。

Progress in cell cycle research Pub Date : 2003-01-01
Ainslie B Parsons, Ron Geyer, Timothy R Hughes, Charles Boone
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引用次数: 0

摘要

小的、细胞可渗透的、靶向性的化学配体不仅作为治疗药物而且作为研究工具都具有很高的价值。这些化合物的合成、鉴定和表征往往是一项艰巨的任务。出芽酵母酿酒酵母的直接遗传学,以及酵母和高等生物之间基本细胞过程的高度保守性,使酵母成为药物开发研究的绝佳工具,特别是在抗癌和抗真菌药物发现方面。酵母功能基因组学和蛋白质组学研究的最新进展正在改变酵母研究的领域。许多这些新技术很容易应用于药物靶点鉴定和药物发现的其他方面。本文将重点介绍酿酒葡萄球菌目前的遗传、基因组学和蛋白质组学方法,这些方法在药物发现和靶点验证中具有潜在的应用价值。
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Yeast genomics and proteomics in drug discovery and target validation.

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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The contemporary drug development process: advances and challenges in preclinical and clinical development. Yeast genomics and proteomics in drug discovery and target validation. Proteomic approaches for the identification of cell cycle-related drug targets. Mining the NCI screening database: explorations of agents involved in cell cycle regulation. The role of cytosolic phospholipase A2 in cell cycle progression.
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