Identification of small-molecule inhibitors of the human S100B-p53 interaction and evaluation of their activity in human melanoma cells

被引:15
|
作者
Yoshimura, Chihoko [1 ,2 ]
Miyafusa, Takamitsu [1 ]
Tsumoto, Kouhei [1 ,2 ,3 ]
机构
[1] Univ Tokyo, Inst Med Sci, Med Prote Lab, Tokyo, Japan
[2] Univ Tokyo, Dept Med Genome Sci, Grad Sch Frontier Sci, Tokyo, Japan
[3] Univ Tokyo, Dept Chem & Biotechnol, Sch Engn, Tokyo, Japan
关键词
S100B; p53; Protein-protein interaction; Surface plasomon resonance; Fragment; Inhibitor; NUCLEAR-MAGNETIC-RESONANCE; BINDING PROTEIN S100B; MALIGNANT-MELANOMA; CALCIUM-BINDING; P53; PENTAMIDINE; APOPTOSIS; TARGET; GROWTH; SITES;
D O I
10.1016/j.bmc.2012.12.042
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
The interaction between human S100 calcium-binding protein B (S100B) and the tumor suppressor protein p53 is considered to be a possible therapeutic target for malignant melanoma. To identify potent inhibitors of this interaction, we screened a fragment library of compounds by means of a fluorescence-based competition assay involving the S100B-binding C-terminal peptide of p53. Using active compounds from the fragment library as query compounds, we constructed a focused library by means of two-dimensional similarity searching of a large database. This simple, unbiased method allowed us to identify several inhibitors of the S100B-p53 interaction, and we elucidated preliminary structure-activity relationships. One of the identified compounds had the potential to inhibit the S100B-p53 interaction in melanoma cells. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1109 / 1115
页数:7
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