dc.contributor.author
Anderson, Elizabeth
dc.contributor.author
Stavenhagen, Kathrin
dc.contributor.author
Kolarich, Daniel
dc.contributor.author
Sommerhoff, Christian P.
dc.contributor.author
Maurer, Marcus
dc.contributor.author
Metz, Martin
dc.date.accessioned
2019-04-11T07:30:08Z
dc.date.available
2019-04-11T07:30:08Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/24370
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-2142
dc.description.abstract
Snake envenoming is a serious and neglected public health crisis that is responsible for as many as 125,000 deaths per year, which is one of the reasons the World Health Organization has recently reinstated snakebite envenoming to its list of category A neglected tropical diseases. Here, we investigated the ability of human mast cell proteases to detoxify six venoms from a spectrum of phylogenetically distinct snakes. To this end, we developed a zebrafish model to assess effects on the toxicity of the venoms and characterized the degradation of venom proteins by mass spectrometry. All snake venoms tested were detoxified by degradation of various venom proteins by the mast cell protease tryptase beta, and not by other proteases. Our data show that recombinant human tryptase beta degrades and detoxifies a phylogenetically wide range of venoms, indicating that recombinant human tryptase could possibly be developed as a universal antidote to venomous snakebites.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Human mast cell tryptase is a potential treatment for snakebite envenoming across multiple snake species
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
1532
dcterms.bibliographicCitation.doi
10.3389/fimmu.2018.01532
dcterms.bibliographicCitation.journaltitle
Frontiers in Immunology
dcterms.bibliographicCitation.originalpublishername
Frontiers Media S.A.
dcterms.bibliographicCitation.volume
9
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
30038613
dcterms.isPartOf.issn
1664-3224