Universal building blocks for antigen presentation to uncover the flavivirus-directed antibody response
The FLAVIR project aims to develop a structural proteomics toolkit using mass spectrometry and electron microscopy to enhance understanding of neutralizing antibody responses against flaviviruses for vaccine development.
Projectdetails
Introduction
Flaviviruses are a tremendous burden on global public health. The genus consists of yellow fever virus, dengue virus, and zika virus amongst others. These viruses threaten more than half the global human population and are spreading into new territories. The recent zika virus pandemic stresses the need for a suitable protein engineering toolkit to enable swift development of emerging flavivirus antigens for structural studies, serology, and vaccine development.
Challenges in Understanding Antibody Responses
Moreover, the structural determinants of a neutralizing polyclonal antibody response are currently not well understood, in large part due to a lack of suitable methods to address the complex interactions of multiple antibodies directed against a heterogeneous, glycosylated viral antigen.
Project Overview
With FLAVIR, I will use my unique expertise in both mass spectrometry and electron microscopy to develop a comprehensive structural proteomics toolkit for in-depth profiling of the neutralizing antibody response against flaviviruses.
Methodology
Using a combination of:
- Novel mass spectrometry-based antibody sequencing techniques
- Glycoproteomics profiling
- Electron microscopy
We will uncover how the polyclonal antibody response against flaviviruses is directed by key structural determinants of the Envelope glycoprotein that is displayed on the surface of infectious virions.
Development of New Strategies
We will develop new strategies to produce prefusion stabilized E-dimers and ultimately reconstruct full icosahedral flavivirus-like particles from soluble components.
Testing and Streamlining
The outlined strategies will be tested and streamlined for broad applicability across the flaviviruses so that they can be swiftly adapted for emerging species and strains. We will characterize our designs with state-of-the-art mass spectrometry methods (native MS, mass photometry, HDX-MS) and electron microscopy.
Antigen Optimization and Analysis
We will use these optimized antigens to uncover the role of antigen glycosylation in antibody binding, profile the serum antibody repertoire directed against the E-antigen, and map out...
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.687.500 |
Totale projectbegroting | € 1.687.500 |
Tijdlijn
Startdatum | 1-8-2023 |
Einddatum | 31-7-2028 |
Subsidiejaar | 2023 |
Partners & Locaties
Projectpartners
- UNIVERSITEIT UTRECHTpenvoerder
Land(en)
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