HOPPI-NMR: Hot-Peptide-Based Screening Assay for Inhibitors of Protein-Protein Interactions by NMR

被引:4
作者
Brancaccio, Diego [1 ]
Di Maro, Salvatore [2 ]
Cerofolini, Linda [3 ]
Giuntini, Stefano [3 ]
Fragai, Marco [3 ]
Luchinat, Claudio [3 ]
Tomassi, Stefano [1 ]
Limatola, Antonio [4 ]
Russomanno, Pasquale [1 ]
Merlino, Francesco [1 ]
Novellino, Ettore [1 ]
Carotenuto, Alfonso [1 ]
机构
[1] Univ Naples Federico II, Dept Pharm, I-80131 Naples, Italy
[2] Univ Campania Luigi Vanvitelli, DISTABIF, I-81100 Caserta, Italy
[3] Univ Florence, CERM, I-50019 Sesto Fiorentino, Italy
[4] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
来源
ACS MEDICINAL CHEMISTRY LETTERS | 2020年 / 11卷 / 05期
关键词
TRANSFER DIFFERENCE NMR; STAPLED PEPTIDES; LIGAND-BINDING; P53; MDM2; PHOSPHORYLATION; ACTIVATION;
D O I
10.1021/acsmedchemlett.9b00620
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Protein-protein interactions (PPIs) contribute to the onset and/or progression of several diseases, especially cancer, and this discovery has paved the way for considering disruption of the PPIs as an attractive anti-tumor strategy. In this regard, simple and efficient biophysical methods for detecting the interaction of the inhibitors with the protein counterpart are still in high demand. Herein, we describe a convenient NMR method for the screening of putative PPI inhibitors based on the use of "hot peptides" (HOPPI-NMR). As a case study, HOPPI-NMR was successful applied to the well-known p53/MDM2 system. Our outcomes highlight the main advantages of the method, including the use of a small amount of unlabeled proteins, the minimization of the risk of protein aggregation, and the ability to identify weak binders. The last leaves open the possibility for application of HOPPI-NMR in tandem with fragment-based drug discovery as a valid strategy for the identification of novel chemotypes acting as PPI inhibitors.
引用
收藏
页码:1047 / 1053
页数:7
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