Stabilization of protein-protein interactions by small molecules

被引:43
|
作者
Giordanetto, Fabrizio [1 ]
Schafer, Anja [2 ,3 ]
Ottmann, Christian [2 ,3 ]
机构
[1] Taros Chem, Med Chem, D-44227 Dortmund, Germany
[2] Tech Univ Eindhoven, Biol Chem Lab, NL-5612 AZ Eindhoven, Netherlands
[3] Tech Univ Eindhoven, Dept Biomed Engn, Inst Complex Mol Syst, NL-5612 AZ Eindhoven, Netherlands
关键词
DIFFERENTIATION-INDUCING AGENT; CYTOSOLIC BINDING-PROTEIN; DNA TOPOISOMERASE-II; CYCLOSPORINE-A; ADENYLATE-CYCLASE; SMALL-CONDUCTANCE; FORSKOLIN DERIVATIVES; RAPAMYCIN ANALOGS; CRYSTAL-STRUCTURE; COTYLENIN-A;
D O I
10.1016/j.drudis.2014.08.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Protein-protein interactions (PPIs) are implicated in every disease and mastering the ability to influence PPIs with small molecules would considerably enlarge the druggable genome. Whereas inhibition of PPIs has repeatedly been shown to work successfully, targeted stabilization of PPIs is underrepresented in the literature. This is all the more surprising because natural products like FK506, rapamycin, brefeldin, forskolin and fusicoccin confer their physiological activity by stabilizing specific PPIs. However, recently a number of very interesting synthetic molecules have been reported from drug discovery projects that indeed achieve their desired activities by stabilizing either homo- or hetero-oligomeric complexes of their target proteins.
引用
收藏
页码:1812 / 1821
页数:10
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