Environment-sensitive turn-on fluorescent probes for p53-MDM2 protein-protein interaction

被引:11
作者
Liu, Tingting [1 ]
Jiang, Yan [2 ]
Liu, Zhenzhen [1 ]
Li, Jin [2 ]
Fang, Kun [2 ]
Zhuang, Chunlin [2 ]
Du, Lupei [1 ]
Fang, Hao [1 ]
Sheng, Chunquan [2 ]
Li, Minyong [1 ]
机构
[1] Shandong Univ, Sch Pharm, Dept Med Chem, Key Lab Chem Biol,MOE, Jinan 250012, Shandong, Peoples R China
[2] Second Mil Med Univ, Sch Pharm, Dept Med Chem, 325 Guohe Rd, Shanghai 200433, Peoples R China
关键词
P53; PROTEIN; TRANSLOCATION; INHIBITION; DISCOVERY;
D O I
10.1039/c7md00287d
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
A series of probes with a turn-on switch for the p53-MDM2 protein-protein interaction were developed. After careful evaluation, these small molecule fluorescent probes exhibited high practical activity and selectivity in vitro and in cellulo. In particular probe 10, which had a K-i value of 0.03 mu M, displayed much better binding affinity compared to the positive control Nutlin-3, which had a K-i value of 0.23 mu M. These no-wash environment-sensitive turn-on fluorescent probes have been successfully applied to imaging p53-MDM2 interaction in the human lung cancer cell line A549 (wild-type p53) at the micromolar level. Therefore, these fluorescent probes are expected to be used in drug screening and cell staining in p53-MDM2 fields, as well as in pathological and physiological studies of the p53-MDM2 interaction.
引用
收藏
页码:1668 / 1672
页数:5
相关论文
共 26 条
[1]   Live-cell imaging of p53 interactions using a novel Venus-based bimolecular fluorescence complementation system [J].
Amaral, Joana Dias ;
Herrera, Federico ;
Rodrigues, Pedro Miguel ;
Dionisio, Pedro Antunes ;
Outeiro, Tiago Fleming ;
Pereira Rodrigues, Cecilia Maria .
BIOCHEMICAL PHARMACOLOGY, 2013, 85 (06) :745-752
[2]   MDM2 EXPRESSION IS INDUCED BY WILD TYPE-P53 ACTIVITY [J].
BARAK, Y ;
JUVEN, T ;
HAFFNER, R ;
OREN, M .
EMBO JOURNAL, 1993, 12 (02) :461-468
[3]  
Chène P, 2004, MOL CANCER RES, V2, P20
[4]   Inhibiting the p53-MDM2 interaction:: An important target for cancer therapy [J].
Chène, P .
NATURE REVIEWS CANCER, 2003, 3 (02) :102-109
[5]  
Esteller M, 1999, CANCER RES, V59, P67
[6]   Biomolecular fluorescence complementation (BiFC) analysis as a probe of protein interactions in living cells [J].
Kerppola, Tom K. .
ANNUAL REVIEW OF BIOPHYSICS, 2008, 37 :465-487
[7]   Development of an autofluorescent translocation biosensor system to investigate protein-protein interactions in living cells [J].
Knauer, SK ;
Stauber, RH .
ANALYTICAL CHEMISTRY, 2005, 77 (15) :4815-4820
[8]   Structure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domain [J].
Kussie, PH ;
Gorina, S ;
Marechal, V ;
Elenbaas, B ;
Moreau, J ;
Levine, AJ ;
Pavletich, NP .
SCIENCE, 1996, 274 (5289) :948-953
[9]   Bright ideas for chemical biology [J].
Lavis, Luke D. ;
Raines, Ronald T. .
ACS CHEMICAL BIOLOGY, 2008, 3 (03) :142-155
[10]   Direct Monitoring of the Inhibition of Protein-Protein Interactions in Cells by Translocation of PKCδ Fusion Proteins [J].
Lee, Kyung-Bok ;
Hwang, Jung Me ;
Choi, Insung S. ;
Rho, Jaerang ;
Choi, Jong-Soon ;
Kim, Gun-Hwa ;
Kim, Seung Il ;
Kim, Soohyun ;
Lee, Zee-Won .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (06) :1314-1317