Development and application of bioprobes for mammalian cell cycle analyses

被引：12
作者：
Osada, H [1 ]
机构：
[1] RIKEN, Antibiot Lab, Wako, Saitama 3510198, Japan
来源：
CURRENT MEDICINAL CHEMISTRY | 2003年 / 10卷 / 09期
关键词：
chemical biology; IleRS; p53; cyclin-dependent kinase; tubulin; kinesin; mitosis; MICROTUBULE-STABILIZING AGENTS; SMALL-MOLECULE INHIBITOR; REVEROMYCIN-A; SACCHAROMYCES-CEREVISIAE; ASPERGILLUS-FUMIGATUS; GROWTH-FACTOR; MICROBIAL METABOLITES; BIOLOGICAL PROPERTIES; CHEMICAL GENETICS; NATURAL-PRODUCTS;
D O I：
10.2174/0929867033457836
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
In this review, I have mainly described the cell cycle inhibitors isolated from microbial metabolites. Once the molecular target of the inhibitor is determined, the inhibitor can be used as bioprobe to dissect the diverse aspect of biological functions in chemical biology research. Reveromycin A and phosmidosine inhibited the protein synthesis of mammalian cells and arrested the cell cycle at G1 phase. Lucilactaene arrested cells at G1 phase through restoration of mutant p53. Tryprostatin A inhibited the microtubule polymerization by interfering with the interaction between tubulin and microtubule associating protein. On the contrary, cyclotryprostatin D, structurally related to tryprostatin A, enhanced the tubulin polymerization. Terpendole E inhibited the motor activity of mitotic kinesin, Eg5 and induced monoastral spindle in M phase.
引用
收藏
页码：727 / 732
页数：6
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