Chemical Genomics Centre of the Max Planck Society, Otto-Hahn-Straße 15, D-44227 Dortmund, Germany.
Chem Commun (Camb). 2013 Oct 4;49(76):8468-70. doi: 10.1039/c3cc44612c.
We report first non-covalent and exclusively extracellular inhibitors of 14-3-3 protein-protein interactions identified by virtual screening. Optimization by crystal structure analysis and in vitro binding assays yielded compounds capable of disrupting the interaction of 14-3-3σ with aminopeptidase N in a cellular assay.
我们报告了首次通过虚拟筛选鉴定的非共价且完全在细胞外的 14-3-3 蛋白-蛋白相互作用抑制剂。通过晶体结构分析和体外结合实验进行优化,得到了能够在细胞实验中破坏 14-3-3σ与氨肽酶 N 相互作用的化合物。