Lead Discovery Center GmbH, Otto-Hahn-Str. 15, 44227 Dortmund, Germany.
Laboratory of Chemical Biology, Department of Biomedical Engineering and Institute for Complex Molecular Systems, Eindhoven University of Technology, Den Dolech 2, 5612 AZ Eindhoven, The Netherlands.
Biochemistry. 2024 Sep 3;63(17):2196-2206. doi: 10.1021/acs.biochem.4c00248. Epub 2024 Aug 22.
The identification of chemical starting points for the development of molecular glues is challenging. Here, we employed fragment screening and identified an allosteric stabilizer of the complex between 14-3-3 and a TAZ-derived peptide. The fragment binds preferentially to the 14-3-3/TAZ peptide complex and shows moderate stabilization in differential scanning fluorimetry and microscale thermophoresis. The binding site of the fragment was predicted by molecular dynamics calculations to be distant from the 14-3-3/TAZ peptide interface, located between helices 8 and 9 of the 14-3-3 protein. This site was confirmed by nuclear magnetic resonance and X-ray protein crystallography, revealing the first example of an allosteric stabilizer for 14-3-3 protein-protein interactions.
开发分子胶的化学起始点的鉴定具有挑战性。在这里,我们采用了片段筛选,并鉴定出了 14-3-3 与 TAZ 衍生肽之间复合物的别构稳定剂。该片段优先与 14-3-3/TAZ 肽复合物结合,并在差示扫描荧光法和微尺度热泳法中表现出适度的稳定性。通过分子动力学计算预测该片段的结合位点远离 14-3-3/TAZ 肽界面,位于 14-3-3 蛋白的 8 号和 9 号螺旋之间。这一位置通过核磁共振和 X 射线蛋白质晶体学得到了证实,揭示了首个针对 14-3-3 蛋白-蛋白相互作用的别构稳定剂的例子。