Skip to main content
Go to the home page of the European Commission (opens in new window)
English en
CORDIS - EU research results
CORDIS

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

Project description

Amyloid fibres in infection

Some proteins can self-assemble into elongated structures known as amyloids, which are linked not only to disease but also to antimicrobial defence and bacterial virulence. However, it remains poorly understood how the shape and structure of these fibres affect their functionality. The goal of the ERC-funded FuncAmyloid project is to investigate amyloid fibres produced by bacteria such as Staphylococcus aureus and Pseudomonas aeruginosa and delineate their role as toxins or in biofilm formation. Researchers will utilise advanced microscopy and structural analysis to understand how different fibre forms interact with cell membranes and cause damage. Project findings will help design new antimicrobial peptides and molecules, paving the way for new strategies to combat infectious diseases.

Objective

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.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

HORIZON-ERC - HORIZON ERC Grants

See all projects funded under this funding scheme

Call for proposal

(opens in new window) ERC-2022-COG

See all projects funded under this call

Host institution

DEUTSCHES ELEKTRONEN-SYNCHROTRON DESY
Net EU contribution
€ 2 000 000,00
Address
NOTKESTRASSE 85
22607 Hamburg
Germany
Region
Hamburg Hamburg Hamburg
Activity type
Research Organisations
Links
Total cost
€ 2 000 000,00

Beneficiaries (2)