Motif mediated protein-protein interactions as drug targets

Cell Communication and Signaling

Review

Carles Corbi-Verge¹  Philip M. Kim² 

[1] Terrence Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, M5S 3E1, Toronto, ON, Canada;Terrence Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, M5S 3E1, Toronto, ON, Canada;Department of Molecular Genetics, University of Toronto, M5S 3E1, Toronto, ON, Canada;Department of Computer Science, University of Toronto, M5S 3E1, Toronto, ON, Canada;

关键词: Protein-protein interactions;    Linear motifs;    Drug discovery;    Small-molecule inhibitors;    Peptidomimetics;    Peptides as therapeutics;   

DOI  :  10.1186/s12964-016-0131-4

 received in 2015-12-30, accepted in 2016-02-25,  发布年份 2016

来源: Springer

【 摘 要 】

Protein-protein interactions (PPI) are involved in virtually every cellular process and thus represent an attractive target for therapeutic interventions. A significant number of protein interactions are frequently formed between globular domains and short linear peptide motifs (DMI). Targeting these DMIs has proven challenging and classical approaches to inhibiting such interactions with small molecules have had limited success. However, recent new approaches have led to the discovery of potent inhibitors, some of them, such as Obatoclax, ABT-199, AEG-40826 and SAH-p53-8 are likely to become approved drugs. These novel inhibitors belong to a wide range of different molecule classes, ranging from small molecules to peptidomimetics and biologicals. This article reviews the main reasons for limited success in targeting PPIs, discusses how successful approaches overcome these obstacles to discovery promising inhibitors for human protein double minute 2 (HDM2), B-cell lymphoma 2 (Bcl-2), X-linked inhibitor of apoptosis protein (XIAP), and provides a summary of the promising approaches currently in development that indicate the future potential of PPI inhibitors in drug discovery.

【 授权许可】

CC BY   
© Corbi-Verge and Kim. 2016