Small-Molecule Stabilization of Protein-Protein Interactions: An Underestimated Concept in Drug Discovery?

被引:156
|
作者
Thiel, Philipp [1 ]
Kaiser, Markus [2 ]
Ottmann, Christian [1 ]
机构
[1] Max Planck Soc, Chem Genom Ctr, D-44227 Dortmund, Germany
[2] Univ Duisburg Essen, Fac Biol, Ctr Med Biotechnol, D-45141 Essen, Germany
关键词
drug design; modulation; protein-protein interaction; small-molecule drugs; stabilization; MAMMALIAN ADENYLYL-CYCLASE; NUCLEOTIDE-EXCHANGE FACTOR; PEPTIDYL-PROLYL ISOMERASE; BREFELDIN-A; SUPEROXIDE-DISMUTASE; IMMUNOSUPPRESSANT FK506; CRYSTAL-STRUCTURE; BINDING-SITE; SEC7; DOMAIN; COMPLEX;
D O I
10.1002/anie.201107616
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The modulation of proteinprotein interactions (PPIs) has been recognized as one of the most challenging tasks in drug discovery. While their systematic development has long been considered as intractable, this view has changed over the last years, with the first drug candidates undergoing clinical studies. To date, the vast majority of PPI modulators are interaction inhibitors. However, in many biological contexts a prolonged lifespan of a PPI might be desirable, calling for the complementary approach of PPI stabilization. In fact, nature offers impressive examples of this concept and some PPI-stabilizing natural products have already found application as important drugs. Moreover, directed small-molecule stabilization has recently been demonstrated. Therefore, it is time to take a closer look at the constructive side of modulating PPIs.
引用
收藏
页码:2012 / 2018
页数:7
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