Issue 9, 2021

Identification of molecular glues of the SLP76/14-3-3 protein–protein interaction

Abstract

The stabilisation of protein–protein interactions (PPIs) through molecular glues is a novel and promising approach in drug discovery. In stark contrast to research in protein–protein inhibition the field of stabilisation remains underdeveloped with comparatively few examples of small-molecule stabilisers of PPIs reported to date. At the same time identifying molecular glues has received recent sustained interest, especially in the fields of targeted protein degradation and 14-3-3 PPIs. The hub-protein 14-3-3 has a broad interactome with more than 500 known protein partners which presents a great opportunity for therapeutic intervention. In this study we have developed an HTRF assay suitable for HTS of the 14-3-3/SLP76 PPI and have completed a proof of concept screen against a chemically diverse library of 20 K molecules. The adaptor protein SLP76 has been reported to interact with 14-3-3 proteins downstream of the TCR playing an important role in mediating its own proteasomal degradation. We believe that stabilisation of this PPI could be exploited to potentiate degradation of SLP76 and therefore inhibit TCR signalling. This would represent an interesting alternative to other approaches in the field of targeted protein degradation. Here we disclose 16 novel stabilisers of the 14-3-3/SLP76 PPI across multiple different chemotypes. Based on the early results presented here we would recommend this approach to find molecular glues with broad applicability in the field of 14-3-3 PPIs.

Graphical abstract: Identification of molecular glues of the SLP76/14-3-3 protein–protein interaction

Supplementary files

Article information

Article type
Research Article
Submitted
19 Maijs 2021
Accepted
01 Jūl. 2021
First published
02 Aug. 2021
This article is Open Access
Creative Commons BY license

RSC Med. Chem., 2021,12, 1555-1564

Identification of molecular glues of the SLP76/14-3-3 protein–protein interaction

L. Soini, M. Redhead, M. Westwood, S. Leysen, J. Davis and C. Ottmann, RSC Med. Chem., 2021, 12, 1555 DOI: 10.1039/D1MD00172H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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