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CORDIS

Structure, Function and Regulation of Antimicrobial and Virulent Amyloids at High-resolution

Descrizione del progetto

Fibre amiloidi nelle infezioni

Alcune proteine possono auto-assemblarsi in strutture allungate note come amiloidi, collegate non solo alle malattie ma anche alla difesa antimicrobica e alla virulenza batterica. Tuttavia, rimane poco chiaro come la forma e la struttura di queste fibre influenzino la loro funzionalità. L’obiettivo del progetto FuncAmyloid, finanziato dal CER, è studiare le fibre amiloidi prodotte da batteri come Staphylococcus aureus e Pseudomonas aeruginosa e delineare il loro ruolo come tossine o nella formazione di biofilm. I ricercatori utilizzeranno la microscopia avanzata e l’analisi strutturale per capire come le diverse forme di fibre interagiscono con le membrane cellulari e causano danni. I risultati del progetto contribuiranno alla progettazione di nuovi peptidi e molecole antimicrobiche, aprendo la strada a nuove strategie per combattere le malattie infettive.

Obiettivo

Self-assembly of proteins and peptides into amyloid fibrils produced across kingdoms of life is associated with antimicrobial activity, microbial pathogenicity, and a wide range of diseases. The correlation of fibrillation and morphology to function is poorly understood, and high-resolution structural information and mechanistic models are lacking. Our lab pioneered the atomic-level analysis of bacterial amyloids and eukaryotic functional fibrils involved in cytotoxicity, biofilm structuring, and antibacterial activity. We revealed novel morphologies extending beyond canonical amyloid cross- structures of tightly mated -sheets, to include, for example, cross- fibrils composed on amphipathic -helices. In addition, we exposed a unique lipid-induced cross-/ secondary structure switch in fibrils of the same sequence. Here we investigate amyloid fibrils which serve as key virulence determinants in S. aureus and Pseudomonas acting as cytotoxins and in biofilm scaffolding, and as antimicrobials produced across different species. We will leverage the knowledge and expertise, and newly emerging methods in electron, light and force microscopy, to understand how fibrillation propensity, fibril morphology and structural switches are connected to function, membrane interactions and toxicity mechanisms at high resolution. The findings are expected to identify structural features that underlie the formation, regulation, and activity of these fibrils, providing advantages in specific environments. Understanding these structure-function relationships will help to clarify the link between amyloid formation and antimicrobial activity. We will use the insights gained from these studies for the rational design of antimicrobial peptides and small molecules targeting virulent determinants towards potential applications in the management of infectious diseases. Our findings on functional amyloids can overall advance life, material, medical and environmental sciences.

Campo scientifico (EuroSciVoc)

Parole chiave

Programma(i)

Argomento(i)

Meccanismo di finanziamento

HORIZON-ERC - HORIZON ERC Grants

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Invito a presentare proposte

(si apre in una nuova finestra) ERC-2022-COG

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Istituzione ospitante

DEUTSCHES ELEKTRONEN-SYNCHROTRON DESY
Contributo netto dell'UE
€ 2 000 000,00
Costo totale
€ 2 000 000,00

Beneficiari (2)