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

Grant search

Key facts

  • Disease

    COVID-19
  • Start & end year

    2021
    2023
  • Known Financial Commitments (USD)

    $414,169.81
  • Funder

    Bundesministerium für Bildung und Forschung [German Federal Ministry of Education and Research] (BMBF)
  • Principal Investigator

    Gülsah Gabriel
  • Research Location

    Germany
  • Lead Research Institution

    Heinrich-Pette-Institut, Leibniz-Institut für Experimentelle Virologie
  • Research 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.