Issue 3, 2023

Protein–protein interfaces in molecular glue-induced ternary complexes: classification, characterization, and prediction

Abstract

Molecular glues are a class of small molecules that stabilize the interactions between proteins. Naturally occurring molecular glues are present in many areas of biology where they serve as central regulators of signaling pathways. Importantly, several clinical compounds act as molecular glue degraders that stabilize interactions between E3 ubiquitin ligases and target proteins, leading to their degradation. Molecular glues hold promise as a new generation of therapeutic agents, including those molecular glue degraders that can redirect the protein degradation machinery in a precise way. However, rational discovery of molecular glues is difficult in part due to the lack of understanding of the protein–protein interactions they stabilize. In this review, we summarize the structures of known molecular glue-induced ternary complexes and the interface properties. Detailed analysis shows different mechanisms of ternary structure formation. Additionally, we also review computational approaches for predicting protein–protein interfaces and highlight the promises and challenges. This information will ultimately help inform future approaches for rational molecular glue discovery.

Graphical abstract: Protein–protein interfaces in molecular glue-induced ternary complexes: classification, characterization, and prediction

Article information

Article type
Review Article
Submitted
27 Sep 2022
Accepted
02 Jan 2023
First published
03 Jan 2023
This article is Open Access
Creative Commons BY-NC license

RSC Chem. Biol., 2023,4, 192-215

Protein–protein interfaces in molecular glue-induced ternary complexes: classification, characterization, and prediction

H. Rui, K. S. Ashton, J. Min, C. Wang and P. R. Potts, RSC Chem. Biol., 2023, 4, 192 DOI: 10.1039/D2CB00207H

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements