CORONA - ViKon - Targeted elimination of SARS-CoV-2 by microparticle-based high-affinity Visrus binding conjugates; subproject 4: Microparticle-mediated inhibition of SARS-CoV-2 replication in vitro.
- Funded by Bundesministerium für Bildung und Forschung [German Federal Ministry of Education and Research] (BMBF)
- Total publications:0 publications
Grant number: 03COV17D
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Key facts
Disease
COVID-19Start & end year
20212023Known Financial Commitments (USD)
$414,169.81Funder
Bundesministerium für Bildung und Forschung [German Federal Ministry of Education and Research] (BMBF)Principal Investigator
Gülsah GabrielResearch Location
GermanyLead Research Institution
Heinrich-Pette-Institut, Leibniz-Institut für Experimentelle VirologieResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnostics
Research Subcategory
Pathogen morphology, shedding & natural history
Special Interest Tags
N/A
Study Type
Non-Clinical
Clinical Trial Details
N/A
Broad Policy Alignment
Pending
Age Group
Not Applicable
Vulnerable Population
Not applicable
Occupations of Interest
Not applicable
Abstract
The subproject applied for here is part of the joint project "Targeted elimination of SARS-CoV-2 by microparticle-based high-affinity virus-binding conjugates". In this subproject, libraries of virus-binding conjugates (VBK) will be investigated in vitro for their potential to inhibit cell entry and thus replication of SARS-CoV-2. These analyses require biological protection level 3 (BSL-3 laboratory), which is given at the Heinrich Pette Institute (HPI). In the present subproject, mainly a human lung cell line (Calu-3) will be used, which has been identified in preliminary studies as a very good in vitro model for SARS-CoV-2 infections. The planned inhibition assays will be optimized stepwise in a time- and dose-dependent manner to achieve an optimal inhibition of viral replication. Subsequently, the best candidates will be further validated and characterized in primary human lung cells. All necessary techniques to achieve these goals will be routinely performed in Prof. Gabriel's group at HPI. Thus, the final goal of this subproject is the identification, validation and characterization of one or more VBCs with maximal inhibition of SARS-CoV-2 in vitro.