ADDovenom: Thermostable Protein-Based ADDomer Nanoparticles as New Therapeutics for Snakebite Envenoming

Stefanie K Menzies*, Raquel Arinto-Garcia, Fernanda Gobbi Amorim, Iara Aimê Cardoso, Camille Abada, Thomas Crasset, Fabien Durbesson, Rebecca J Edge, Priscila El-Kazzi, Sophie Hall, Damien Redureau, Richard Stenner, Johara Boldrini-França, Huan Sun, António Roldão, Paula M Alves, Robert A Harrison, Renaud Vincentelli, Imre Berger, Loïc QuintonNicholas R Casewell, Christiane Schaffitzel

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

1 Citation (Scopus)

Abstract

Snakebite envenoming can be a life-threatening medical emergency that requires prompt medical intervention to neutralise the effects of venom toxins. Each year up to 138,000 people die from snakebites and threefold more victims suffer life-altering disabilities. The current treatment of snakebite relies solely on antivenom-polyclonal antibodies isolated from the plasma of hyperimmunised animals-which is associated with numerous deficiencies. The ADDovenom project seeks to deliver a novel snakebite therapy, through the use of an innovative protein-based scaffold as a next-generation antivenom. The ADDomer is a megadalton-sized, thermostable synthetic nanoparticle derived from the adenovirus penton base protein; it has 60 high-avidity binding sites to neutralise venom toxins. Here, we outline our experimental strategies to achieve this goal using state-of-the-art protein engineering, expression technology and mass spectrometry, as well as in vitro and in vivo venom neutralisation assays. We anticipate that the approaches described here will produce antivenom with unparalleled efficacy, safety and affordability.

Original languageEnglish
Article number673
JournalToxins
Volume15
Issue number12
DOIs
Publication statusPublished - 28 Nov 2023

Bibliographical note

Funding Information:
This work is supported by a Horizon 2020 FET OPEN grant ‘ADDovenom’ (899670).

Publisher Copyright:
© 2023 by the authors.

Research Groups and Themes

  • Bristol BioDesign Institute
  • Max Planck Bristol

Keywords

  • Animals
  • Humans
  • Snake Bites/drug therapy
  • Antivenins
  • Toxins, Biological
  • Binding Sites
  • Plasma

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