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Unraveling the impact of pathological Tau phosphorylations on the early Tau interactome in Alzheimer's disease

Project description

Tau interactions in health and disease

The Tau protein is predominantly expressed in neurons and associates with the cytoskeleton to maintain cell structure and polarity. In Alzheimer’s disease, Tau becomes abnormally modified, misfolds and forms toxic aggregates that disrupt brain function. While its role in advanced stages of the disease is known, it remains unclear how Tau changes to become toxic. With the support of the Marie Skłodowska-Curie Actions programme, the Tau-Stick2Me project aims to investigate early interactions of Tau before it forms pathological tangles. Using advanced biochemical and proteomic tools, researchers hope to identify the proteins that interact with Tau and determine how this interplay changes in pathology. Project insights could reveal new molecular targets for neurodegenerative diseases.

Objective

The Tau protein during Alzheimer's disease (AD) becomes hyperphosphorylated, misfolds, and aggregates into neurofibrillary tangles (NFTs). Despite knowing the involvement of Tau in AD, the exact mechanism that drives Tau-mediated toxicity is largely unclear. Studying the Tau interactome is an excellent way to decipher the mechanism of Tau toxicity. Most interactome studies have primarily focused on Tau interactions related to NFTs, which represent the mature form of aggregated Tau. This emphasis has led to the overlooking of early-stage Tau interactions, mainly due to the lack of tools to access early Tau forms. My aim is to investigate the Tau interactome at these early stages, which are crucial in AD pathology.
I hypothesize that extensive phosphorylation of Tau in the early stages of AD significantly alters its protein interaction network. This alteration contributes to Tau aggregation and subsequent toxicity in AD. To address this hypothesis, I will use an interdisciplinary approach to systematically identify interacting proteins associated with early Tau forms (non-phosphorylated, site-specifically phosphorylated, and hyperphosphorylated). I will use a protein semisynthesis technique to generate early Tau forms and employ affinity purification-mass spectrometry to identify the interactome associated with them from human brain tissue. Unique interacting proteins of Tau forms detected from the proteomic data, will be assessed in high-throughput Tau biosensor-based cellular screening to identify potential Tau aggregation modifiers. Finally, in vitro biophysical studies will be conducted to characterize the molecular interactions between Tau modifiers and Tau forms. The findings from this project will advance our mechanistic understanding of Tau phosphorylations in AD, elucidate the complex molecular interactions and pathways involved, and pave the way for the development of innovative therapeutic strategies targeting early Tau interactome.

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HORIZON-TMA-MSCA-PF-EF - HORIZON TMA MSCA Postdoctoral Fellowships - European Fellowships

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Call for proposal

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(opens in new window) HORIZON-MSCA-2024-PF-01

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Coordinator

VIB VZW
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.

€ 216 240,00
Address
SUZANNE TASSIERSTRAAT 1
9052 ZWIJNAARDE - GENT
Belgium

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Region
Vlaams Gewest Prov. Oost-Vlaanderen Arr. Gent
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Research Organisations
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