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Highly potent anti-SARS-CoV-2 multi-DARPin therapeutic candidates
Marcel Walser; Sylvia Rothenberger; Daniel L. Hurdiss; Anja Schlegel; Valerie Calabro; Simon Fontaine; Denis Villemagne; Maria Paladino; Tanja Hospodarsch; Alexandra Neculcea; Andreas Cornelius; Patricia Schildknecht; Mirela Matzner; Martin Haenggi; Marco Franchini; Yvonne Kaufmann; Doris Schaible; Iris Schlegel; Chloe Iss; Thamar Looser; Susanne Mangold; Christel Herzog; Dieter Schiegg; Christian Reichen; Filip Radom; Andreas Bosshart; Andreas Lehmann; Micha A. Haeuptle; Alexander Zuercher; Toni Vagt; Gabriel Sigrist; Marcel Straumann; Karl Proba; Niina Veitonmaki; Keith M. Dawson; Christof Zitt; Jennifer Mayor; Sarah Ryter; Heyrhyoung Lyoo; Chunyan Wang; Wentao Li; Ieva Drulyte; Wenjuan Du; H. Kaspar Binz; Leon de Waal; Koert J. Stittelaar; Sarah Taplin; Seth Lewis; Daniel Steiner; Frank J.M. van Kuppeveld; Olivier Engler; Berend-Jan Bosch; Michael T. Stumpp; Patrick Amstutz.
Affiliation
  • Marcel Walser; Molecular Partners AG
  • Sylvia Rothenberger; Spiez Laboratory
  • Daniel L. Hurdiss; Utrecht University
  • Anja Schlegel; Molecular Partners AG
  • Valerie Calabro; Molecular Partners AG
  • Simon Fontaine; Molecular Partners AG
  • Denis Villemagne; Molecular Partners AG
  • Maria Paladino; Molecular Partners AG
  • Tanja Hospodarsch; Molecular Partners AG
  • Alexandra Neculcea; Molecular Partners AG
  • Andreas Cornelius; Molecular Partners AG
  • Patricia Schildknecht; Molecular Partners AG
  • Mirela Matzner; Molecular Partners AG
  • Martin Haenggi; Molecular Partners AG
  • Marco Franchini; Molecular Partners AG
  • Yvonne Kaufmann; Molecular Partners AG
  • Doris Schaible; Molecular Partners AG
  • Iris Schlegel; Molecular Partners AG
  • Chloe Iss; Molecular Partners AG
  • Thamar Looser; Molecular Partners AG
  • Susanne Mangold; Molecular Partners AG
  • Christel Herzog; Molecular Partners AG
  • Dieter Schiegg; Molecular Partners AG
  • Christian Reichen; Molecular Partners AG
  • Filip Radom; Molecular Partners AG
  • Andreas Bosshart; Molecular Partners AG
  • Andreas Lehmann; Molecular Partners AG
  • Micha A. Haeuptle; Molecular Partners AG
  • Alexander Zuercher; Molecular Partners AG
  • Toni Vagt; Molecular Partners AG
  • Gabriel Sigrist; Molecular Partners AG
  • Marcel Straumann; Molecular Partners AG
  • Karl Proba; Molecular Partners AG
  • Niina Veitonmaki; Molecular Partners AG
  • Keith M. Dawson; Molecular Partners AG
  • Christof Zitt; Molecular Partners AG
  • Jennifer Mayor; Spiez Laboratory
  • Sarah Ryter; Spiez Laboratory
  • Heyrhyoung Lyoo; Utrecht University
  • Chunyan Wang; Utrecht University
  • Wentao Li; Utrecht University
  • Ieva Drulyte; Thermo Fisher Scientific
  • Wenjuan Du; Utrecht University
  • H. Kaspar Binz; Molecular Partners AG
  • Leon de Waal; Viroclinics Xplore
  • Koert J. Stittelaar; Viroclinics Xplore
  • Sarah Taplin; Integrated Biologix
  • Seth Lewis; Molecular Partners AG
  • Daniel Steiner; Molecular Partners AG
  • Frank J.M. van Kuppeveld; Utrecht University
  • Olivier Engler; Spiez Laboratory
  • Berend-Jan Bosch; Utrecht University
  • Michael T. Stumpp; Molecular Partners AG
  • Patrick Amstutz; Molecular Partners AG
Preprint in English | bioRxiv | ID: ppbiorxiv-256339
ABSTRACT
Globally accessible therapeutics against SARS-CoV-2 are urgently needed. Here, we report the generation of the first anti-SARS-CoV-2 DARPin molecules with therapeutic potential as well as rapid large-scale production capabilities. Highly potent multivalent DARPin molecules with low picomolar virus neutralization efficacies were generated by molecular linkage of three different monovalent DARPin molecules. These multivalent DARPin molecules target various domains of the SARS-CoV-2 spike protein, thereby limiting possible viral escape. Cryo-EM analysis of individual monovalent DARPin molecules provided structural explanations for the mode of action. Analysis of the protective efficacy of one multivalent DARPin molecule in a hamster SARS-CoV-2 infection model demonstrated a significant reduction of pathogenesis. Taken together, the multivalent DARPin molecules reported here, one of which has entered clinical studies, constitute promising therapeutics against the COVID-19 pandemic.
License
cc_by_nc_nd
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Prognostic study Language: English Year: 2020 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Prognostic study Language: English Year: 2020 Document type: Preprint
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