Stabilization of Protein Protein Interactions; transforming molecular glue discovery from art into science
This project aims to mechanistically understand and stabilize protein-protein interactions involving 14-3-3 to discover molecular glues for targeting intrinsically disordered proteins in neurodegenerative diseases.
Projectdetails
Introduction
Intrinsically Disordered Proteins (IDPs) represent one of drug discovery’s major challenges. Due to their high degree of conformational freedom, IDPs have no defined pockets for binding small molecules.
Molecular Glues in Drug Discovery
Molecular glues that can strengthen protein-protein interactions (PPIs) are a revolutionary technology for drug discovery. The hub protein 14-3-3 regulates many IDPs via phosphorylation-dependent PPIs. Stabilization of 14-3-3 PPIs with small molecular glues provides a unique entry point to render IDPs druggable and mitigate the aberrant behavior of malfunctioning IDPs, for example in neurodegenerative diseases.
Current Challenges
While inhibition of PPIs by small molecules has expanded the proteome suitable for therapeutic intervention, the opposite chemical-biology strategy of PPI stabilization by small molecular glues is, despite a recent surge of interest, remarkably underexplored. The lack of mechanistic understanding of PPI stabilization impedes systematically identifying molecular glues and limits progress to drug IDPs.
Proposed Approach
Based on compelling preliminary data, I propose here that mechanistic understanding of 14-3-3 PPI stabilization will play a crucial role in the discovery of molecular glues for IDPs and transform molecular glue drug discovery from art into science.
Key Objectives
We will tackle this central question by pursuing two key objectives:
-
Mechanistically understand PPI stabilization between the 14-3-3 scaffold protein and IDPs. This will address the underlying thermodynamic and kinetic processes, conformational selection, multivalency, cooperativity, and selectivity.
-
Drugging the undruggable - biomolecular condensates and IDPs - via PPI stabilization approaches. The potential for PPI stabilization in the dense environments of biomolecular condensates will be uncovered, and a mechanism-driven campaign to identify molecular glues for the 14-3-3/Tau PPI will lead the way to novel drug discovery for neurodegenerative diseases.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 2.496.596 |
Totale projectbegroting | € 2.496.596 |
Tijdlijn
Startdatum | 1-9-2023 |
Einddatum | 31-8-2028 |
Subsidiejaar | 2023 |
Partners & Locaties
Projectpartners
- TECHNISCHE UNIVERSITEIT EINDHOVENpenvoerder
Land(en)
Vergelijkbare projecten binnen European Research Council
Project | Regeling | Bedrag | Jaar | Actie |
---|---|---|---|---|
MANUNKIND: Determinants and Dynamics of Collaborative ExploitationThis project aims to develop a game theoretic framework to analyze the psychological and strategic dynamics of collaborative exploitation, informing policies to combat modern slavery. | ERC STG | € 1.497.749 | 2022 | Details |
Elucidating the phenotypic convergence of proliferation reduction under growth-induced pressureThe UnderPressure project aims to investigate how mechanical constraints from 3D crowding affect cell proliferation and signaling in various organisms, with potential applications in reducing cancer chemoresistance. | ERC STG | € 1.498.280 | 2022 | Details |
Uncovering the mechanisms of action of an antiviral bacteriumThis project aims to uncover the mechanisms behind Wolbachia's antiviral protection in insects and develop tools for studying symbiont gene function. | ERC STG | € 1.500.000 | 2023 | Details |
The Ethics of Loneliness and SociabilityThis project aims to develop a normative theory of loneliness by analyzing ethical responsibilities of individuals and societies to prevent and alleviate loneliness, establishing a new philosophical sub-field. | ERC STG | € 1.025.860 | 2023 | Details |
MANUNKIND: Determinants and Dynamics of Collaborative Exploitation
This project aims to develop a game theoretic framework to analyze the psychological and strategic dynamics of collaborative exploitation, informing policies to combat modern slavery.
Elucidating the phenotypic convergence of proliferation reduction under growth-induced pressure
The UnderPressure project aims to investigate how mechanical constraints from 3D crowding affect cell proliferation and signaling in various organisms, with potential applications in reducing cancer chemoresistance.
Uncovering the mechanisms of action of an antiviral bacterium
This project aims to uncover the mechanisms behind Wolbachia's antiviral protection in insects and develop tools for studying symbiont gene function.
The Ethics of Loneliness and Sociability
This project aims to develop a normative theory of loneliness by analyzing ethical responsibilities of individuals and societies to prevent and alleviate loneliness, establishing a new philosophical sub-field.
Vergelijkbare projecten uit andere regelingen
Project | Regeling | Bedrag | Jaar | Actie |
---|---|---|---|---|
Chemical rewiring of E3 ubiquitin ligases as a generalizable therapeutic approachTrickE3 aims to systematically develop monovalent degraders to target undruggable proteins in pancreatic cancer, enhancing drug discovery and expanding the human proteome's targetable space. | ERC STG | € 1.499.625 | 2022 | Details |
Protein-RNA interaction stabilization using molecular gluesThis project aims to develop PRIGLUEs to stabilize RNA-protein interactions, enhancing mRNA splicing and potentially leading to novel therapeutic tools for RNA biology. | ERC STG | € 1.500.000 | 2023 | Details |
ADPribosylation and Ubiquitination; post-translational interplayThis project aims to investigate the interplay between ubiquitination and ADPribosylation in cellular processes to develop novel therapeutic strategies for diseases like infections and cancer. | ERC COG | € 1.999.625 | 2024 | Details |
Exploring the molecular grammar of IDP assembly and condensation at ultra-high throughputEMMA aims to revolutionize the understanding of intrinsically disordered proteins by using mRNA display to evaluate the assembly kinetics and thermodynamics of vast sequence libraries. | ERC COG | € 1.995.554 | 2023 | Details |
Chemical rewiring of E3 ubiquitin ligases as a generalizable therapeutic approach
TrickE3 aims to systematically develop monovalent degraders to target undruggable proteins in pancreatic cancer, enhancing drug discovery and expanding the human proteome's targetable space.
Protein-RNA interaction stabilization using molecular glues
This project aims to develop PRIGLUEs to stabilize RNA-protein interactions, enhancing mRNA splicing and potentially leading to novel therapeutic tools for RNA biology.
ADPribosylation and Ubiquitination; post-translational interplay
This project aims to investigate the interplay between ubiquitination and ADPribosylation in cellular processes to develop novel therapeutic strategies for diseases like infections and cancer.
Exploring the molecular grammar of IDP assembly and condensation at ultra-high throughput
EMMA aims to revolutionize the understanding of intrinsically disordered proteins by using mRNA display to evaluate the assembly kinetics and thermodynamics of vast sequence libraries.