Menzies, Stefanie K. and Arinto-Garcia, Raquel and Amorim, Fernanda Gobbi and Cardoso, Iara Aimê and Abada, Camille and Crasset, Thomas and Durbesson, Fabien and Edge, Rebecca J. and El-Kazzi, Priscila and Hall, Sophie and Redureau, Damien and Stenner, Richard and Boldrini-França, Johara and Sun, Huan and Roldão, António and Alves, Paula M. and Harrison, Robert A. and Vincentelli, Renaud and Berger, Imre and Quinton, Loïc and Casewell, Nicholas R. and Schaffitzel, Christiane (2023) ADDovenom : Thermostable Protein-Based ADDomer Nanoparticles as New Therapeutics for Snakebite Envenoming. Toxins, 15 (12): 673. ISSN 2072-6651
Full text not available from this repository.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.