GOLGITACs: Targeted Degradation of Golgi Apparatus residing Carbohydrate Processing Enzymes
SWEET DEGRADATION aims to develop GolgiTACs for targeted protein degradation of carbohydrate processing enzymes, offering new therapeutic strategies for glycan-related diseases.
Projectdetails
Introduction
Oligosaccharides and glycoconjugates, a hugely diverse class of biomolecules, are closely associated with health and many diseases. Carbohydrate metabolism relies mainly on glycosidases and glycosyltransferases, which are carbohydrate processing enzymes (CPEs) that break and create glycosidic bonds, respectively.
Importance of CPEs
Controlling the activities of these enzymes is vital for understanding pathological processes in, and developing therapeutics for, glycan-related diseases. Recently, new targeted protein degradation (TPD) technologies, which disable disease-related proteins by degradation, have opened possibilities for proteins that are otherwise hard to inhibit.
Limitations of Current Approaches
While TPD within the cytoplasm, cell membrane, and extracellular space can be achieved with current approaches, proteins in the Golgi apparatus cannot be degraded by means of the current methods. Yet, it is a major cellular compartment where most CPEs reside.
Proposed Solution
New TPD strategies targeting Golgi apparatus-resident proteins would be a major solution for CPE-related diseases with unmet medical needs. SWEET DEGRADATION aims to develop strategies that allow for the first time the degradation of proteins located in the Golgi apparatus, opening ways for a new therapeutic modality.
Concept of GolgiTACs
The driving idea behind this proposal is that a molecule can be designed that selects CPEs in the Golgi for targeted protein degradation. Such molecules, which I term GolgiTACs, will link a CPE to a Golgi transporter, either sortilin or cation-independent mannose-6-phosphate receptor (CI-M6PR), and shuttle CPEs to the lysosome for degradation.
Project Aims
- In aim 1, I will focus on developing the GolgiTAC technology.
- In aim 2, GolgiTACs will be exploited for targeted protein degradation of CPEs in disease models.
Conclusion
In all, SWEET DEGRADATION will deliver a conceptually new general strategy to target Golgi proteins for degradation, thus providing new inroads to develop therapeutics for currently untreatable diseases.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.500.000 |
Totale projectbegroting | € 1.500.000 |
Tijdlijn
Startdatum | 1-1-2025 |
Einddatum | 31-12-2029 |
Subsidiejaar | 2025 |
Partners & Locaties
Projectpartners
- UNIVERSITEIT LEIDENpenvoerder
Land(en)
Vergelijkbare projecten binnen European Research Council
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Targeted Protein Degradation as a New Experimental and Therapeutic Approach for Pancreatic Ductal Adenocarcinoma
PROTAC-PDAC aims to develop targeted PROTAC therapies to degrade key oncogenic transcription factors in pancreatic cancer, enhancing treatment efficacy while minimizing toxicity.
Engineering CAR-T cells to overcome glycosylation-driven tumour resistance
The project aims to engineer CAR-T cells that express an enzyme to de-glycosylate tumor cells, enhancing their efficacy against solid cancers by overcoming immunosuppressive barriers.
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.
Targeting of glycosylation pathways to empower CAR-T therapy of solid tumors.
This project aims to enhance CAR-T cell therapy for solid tumors by engineering glycosylation pathways to improve immune response and long-term persistence against immunosuppressive environments.
Glycan Mimetics for Cell Glycocalyx Reconstitution: a polymer chemist’s approach to fight infection
GLYMCE aims to uncover how carbohydrates influence pathogen interactions to create innovative glycopolymer materials for infection prevention and treatment.
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Closed-loop deep learning in early-stage drug discovery - cloud platform for targeted protein degradationCeleris Therapeutics leverages deep learning to develop a web platform for degrading undruggable proteins, aiming to revolutionize drug discovery for incurable diseases like Alzheimer's and cancer. | EIC Accelerator | € 2.500.000 | 2022 | Details |
Precision control of glycosylation to open a new era of therapeutic antibodiesGlycoBoost aims to revolutionize monoclonal antibody design by producing therapeutics with uniform N-glycans, enhancing safety and efficacy for autoimmune disease treatments. | EIC Transition | € 2.499.540 | 2025 | Details |
TraffikGene-Tx: Targeted Peptide Carriers for RNA DeliveryTraffikGene-Tx aims to develop safe, scalable peptide carriers for targeted RNA delivery, addressing genetic diseases and enhancing NAT therapies to improve patient outcomes and reduce healthcare costs. | EIC Transition | € 2.498.963 | 2023 | 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.
Closed-loop deep learning in early-stage drug discovery - cloud platform for targeted protein degradation
Celeris Therapeutics leverages deep learning to develop a web platform for degrading undruggable proteins, aiming to revolutionize drug discovery for incurable diseases like Alzheimer's and cancer.
Precision control of glycosylation to open a new era of therapeutic antibodies
GlycoBoost aims to revolutionize monoclonal antibody design by producing therapeutics with uniform N-glycans, enhancing safety and efficacy for autoimmune disease treatments.
TraffikGene-Tx: Targeted Peptide Carriers for RNA Delivery
TraffikGene-Tx aims to develop safe, scalable peptide carriers for targeted RNA delivery, addressing genetic diseases and enhancing NAT therapies to improve patient outcomes and reduce healthcare costs.