Unfolding the early Htt aggregates: an interdisciplinary approach for characterizing novel molecular events that impact Heat Shock Response in Huntington Disease

Informacje na temat projektu

UnfearHD

Identyfikator umowy o grant: 101130833

DOI

10.3030/101130833

Projekt został zamknięty

Data podpisania przez KE 4 Maja 2023

Data rozpoczęcia 1 Czerwca 2023

Data zakończenia 31 Maja 2025

Finansowanie w ramach

• Widening participation and spreading excellence

Koszt całkowity

Brak danych

Wkład UE

€ 169 326,72

Koordynowany przez

IDRYMA TECHNOLOGIAS KAI EREVNAS
Greece

Periodic Reporting for period 1 - UnfearHD (Unfolding the early Htt aggregates: an interdisciplinary approach for characterizing novel molecular events that impact Heat Shock Response in Huntington Disease)

Okres sprawozdawczy: 2023-06-01 do 2025-05-31

Podsumowanie kontekstu i ogólnych celów projektu

Huntington’s disease (HD) is a hereditary neurodegenerative disorder caused by a pathogenic expansion in the huntingtin (Htt) protein. One of the earliest cellular changes in HD is the failure of proteostasis maintenance, notably the heat shock response (HSR), which protects cells from protein misfolding. The UnfearHD project aimed to decipher how mutant Htt disrupts HSR at the very early stages of disease, using Caenorhabditis elegans as a controlled in vivo model. By leveraging inducible Htt expression and focused molecular profiling, the project intended to define early events leading to neuronal dysfunction and identify potential modifiers of disease progression. This aligns with European strategies for innovation in age‑related health research and supports building capacity for translational neurobiology in Greece

Prace wykonane od początku projektu do końca okresu sprawozdawczego oraz najważniejsze dotychczasowe rezultaty

During the fellowship, I generated new C. elegans strains expressing His‑tagged, inducible Htt‑polyQ constructs (Del, 25Q and 103Q variants), enabling temporal control over mutant protein expression. I identified a narrow early‑adulthood window when the heat shock response (HSR) remains functional despite Htt induction. In parallel, I optimized a BONCAT‑based proteomics workflow to efficiently tag and detect newly synthesized proteins during early proteotoxic stress, establishing a foundation for subsequent large‑scale proteomic profiling. These results provide valuable tools for Huntington’s disease research, and the forthcoming proteomic data are expected to reveal novel pathways involved in early disease processes. Importantly, these achievements also supported my appointment as Assistant Professor in Biochemistry at AUTH

Innowacyjność oraz oczekiwany potencjalny wpływ (w tym dotychczasowe znaczenie społeczno-gospodarcze i szersze implikacje społeczne projektu)

The inducible Htt-expressing nematode model and enhanced BONCAT workflow represent significant methodological advances. They provide a novel, time-resolved platform to study proteostasis dynamics in neurodegeneration models, accessible to other researchers. These tools have already been shared with research groups at IMBB‑FORTH and an external partner lab. The expected long-term impact includes enabling discovery of early biomarkers or modulators of cellular stress relevant for therapeutic research in HD and related disorders

Schematic workflow of the project concept