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Deciphering Neurodegenerative Disease with fast 3D imaging & functional nanoscopy

Project description

Multimodal AI-informed microscopy and functional nanoscopy illuminate disease processes

Neurodegenerative diseases such as Huntington’s disease are progressive brain disorders caused by protein aggregation leading to neurotoxicity. Early processes and underlying mechanisms remain poorly understood. Aberrant liquid-liquid phase separation has been implicated. The ERC-funded QScope project aims to investigate the biophysical basis of aggregate formation and toxicity and the role of phase separation in Huntingdon’s disease using cellular models and in vitro experiments. The project will investigate protein variants, the cellular environment, phase separation and prion-like extracellular protein spreading. Development of multimodal AI-informed microscopy and functional nanoscopy relying on label-free imaging and virtual staining will support assessment of mechanical properties and cell pathophysiology with minimal interference.

Objective

Neurodegenerative diseases are incurable, progressive brain disorders associated with accumulation of aberrant protein aggregates with severe effects on movement and mental functioning. The mechanism leading to neurotoxicity is far from understood, due to our lack of insight into early processes. Recently, aberrant liquid-liquid phase separation has emerged as a new concept to explain protein aggregation in neurodegenerative disease. Here, I will investigate the biophysical basis of the formation of different material states of aggregates, by capitalizing on my expertise at the interface of single-molecule biophysics and quantitative, high-resolution imaging in cells.

I propose to address the following key questions, with the use of cellular models of Huntingtons Disease (HD) complemented with well-controlled in vitro experiments: How do the physico-chemical properties of protein variants and the cellular environment influence aggregation and toxicity? What role does phase separation play in Huntingtons disease? How does prion-like spreading of extracellular protein interfere with local protein assemblies in cells?

HD is caused by a gene defect resulting in aggregation-prone huntingtin protein. The diverse sizes (nm-m) and conformations of the aggregates pose a remarkable challenge, and multiple complementary approaches are needed to unravel their morphology and physico-chemical properties. I will develop multimodal AI-informed quantitative microscopy and functional nanoscopy to decipher how aggregates in neurodegenerative disease form and mature. Importantly, we will work without tags and exploit virtually stained quantitative phase imaging to assess mechanical properties and cell pathophysiology, therefore minimizing interference with aggregation processes. The QScope project is expected to elucidate the role of protein aggregation and phase transitions, relevant for a broad variety of diseases, and to establish new label-free and super-resolution imaging.

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Keywords

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Programme(s)

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Topic(s)

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Funding Scheme

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HORIZON-ERC - HORIZON ERC Grants

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Call for proposal

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(opens in new window) ERC-2024-STG

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Host institution

TECHNISCHE UNIVERSITEIT DELFT
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 1 500 000,00
Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 1 500 000,00

Beneficiaries (1)

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