MDMX公司
平方毫米
化学
离解(化学)
蛋白质-蛋白质相互作用
信号
生物物理学
小分子
聚丙烯酰胺凝胶电泳
P53蛋白
细胞生物学
生物化学
细胞凋亡
生物
酶
物理化学
作者
A. Lamberti,Roberta Sgammato,Doriana Desiderio,Chiara Punzo,Gennaro Raimo,Ettore Novellino,Alfonso Carotenuto,Mariorosario Masullo
标识
DOI:10.1002/elps.201400424
摘要
In the present study, we investigated a new approach for studying the interaction between p53 and MDM2/X (where MDM is murine double minute protein). The method is based on the different mobility between the interacting domains of the oncosuppressor p53 and its protein ligands MDM2/X on polyacrylamide gels under native conditions. While the two proteins MDM2/X alone were able to enter the gel, the formation of a binary complex between p53 and MDM2/X prevented the gel entry. The novel technique is reliable for determining the different affinity elicited by MDM2 or MDMX toward p53, and can be useful for analyzing the dissociation power exerted by other molecules on the p53-MDM2/X complex.
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