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 behaviour 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.
Objectives
We will tackle this central question by pursuing two key objectives:
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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.
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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
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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 Starting... | € 1.500.000 | 2023 | 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 Consolid... | € 1.995.554 | 2023 | Details |
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 Starting... | € 1.499.625 | 2022 | Details |
A general approach for the design of covalent protein proximity inducersThis project aims to expand biochemical perturbations using CoLDR chemistry to create small molecules that activate enzymes, modify PTMs, and control protein interactions for therapeutic applications. | ERC Consolid... | € 1.998.744 | 2024 | Details |
Physical and molecular underpinnings of the multifunctionality of bacterial peptide assembliesThis project aims to uncover the self-assembly mechanisms of phenol soluble modulins in Staphylococcus aureus to understand their multifunctionality and develop novel therapeutics against infections. | ERC Starting... | € 1.500.000 | 2025 | Details |
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.
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.
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.
A general approach for the design of covalent protein proximity inducers
This project aims to expand biochemical perturbations using CoLDR chemistry to create small molecules that activate enzymes, modify PTMs, and control protein interactions for therapeutic applications.
Physical and molecular underpinnings of the multifunctionality of bacterial peptide assemblies
This project aims to uncover the self-assembly mechanisms of phenol soluble modulins in Staphylococcus aureus to understand their multifunctionality and develop novel therapeutics against infections.
Vergelijkbare projecten uit andere regelingen
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Inhibitor-Mediated Programming of GlycoformsThe project aims to revolutionize glycan manipulation using Inhibitor-Mediated Programming of Glycoforms (IMProGlyco) to create precision-engineered therapeutic proteins and enhance cellular functions. | EIC Pathfinder | € 2.998.878 | 2025 | Details |
INCYPRO: A key technology to enable the broad application of proteins in diagnostics and therapeuticsThe INCYPROnext project aims to validate a novel technology for stabilizing proteins, enhancing their utility in biotechnological and biomedical applications, targeting a $170B market. | EIC Transition | € 2.498.750 | 2022 | Details |
The ProM platform: New ways to drug the undruggablePROSION's ProM-platform aims to unlock and target the undruggable 85% of the human proteome, developing new therapies for hard-to-treat diseases like cancer. | EIC Accelerator | € 2.461.375 | 2022 | Details |
Inhibitor-Mediated Programming of Glycoforms
The project aims to revolutionize glycan manipulation using Inhibitor-Mediated Programming of Glycoforms (IMProGlyco) to create precision-engineered therapeutic proteins and enhance cellular functions.
INCYPRO: A key technology to enable the broad application of proteins in diagnostics and therapeutics
The INCYPROnext project aims to validate a novel technology for stabilizing proteins, enhancing their utility in biotechnological and biomedical applications, targeting a $170B market.
The ProM platform: New ways to drug the undruggable
PROSION's ProM-platform aims to unlock and target the undruggable 85% of the human proteome, developing new therapies for hard-to-treat diseases like cancer.