PXD057613
PXD057613 is an original dataset announced via ProteomeXchange.
Dataset Summary
Title | Enhancing the bothropic antivenom through a reverse antivenomics approach |
Description | Antivenoms are the only effective treatment for snakebite envenomation and have saved countless lives over more than a century. Despite its value, antivenoms often present risks of adverse reactions. Current formulations contain a substantial fraction of non-specific antibodies and serum proteins that do not neutralize venom toxins. While new alternatives are being researched and promising candidates emerge as the next generation of antivenoms, it remains clear that animal-derived antivenoms will still play a critical role for years to come. And current antivenom formulations could still be optimized for safety and efficacy. In this study, we used a reverse antivenomics approach to improve the bothropic antivenom (BAv), capturing toxin-specific antibodies through affinity chromatography using Bothrops jararaca venom toxins immobilized on CNBr-activated resin. This process produced an improved antivenom formulation (iBAv) enriched in neutralizing antibodies and depleted of serum protein contaminants. Proteomic analysis showed that iBAv was 87% depleted in albumin and 37-83% lower in other serum proteins compared to the original BAv. Functional assessments demonstrated that iBAv had a 2.9-fold higher affinity for B. jararaca venom toxins via surface plasmon resonance and a 2.8-fold lower ED50 in vivo in a mice model, indicating enhanced potency and efficacy. Our findings suggest that enriching specific neutralizing antibodies while depleting serum proteins may reduce the overall protein dose required and potentially decrease the risk of adverse reactions. Although technical and economic considerations remain for large-scale implementation, this affinity-enriched antivenom formulation represents a significant advancement in enhancing antivenom efficacy against Bothrops jararaca envenomations. |
HostingRepository | MassIVE |
AnnounceDate | 2025-01-24 |
AnnouncementXML | Submission_2025-01-24_05:19:14.362.xml |
DigitalObjectIdentifier | |
ReviewLevel | Non peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Supported dataset by repository |
PrimarySubmitter | Alexandre Keiji Tashima |
SpeciesList | scientific name: Equus caballus; common name: horse; NCBI TaxID: 9796; |
ModificationList | S-carboxamidomethyl-L-cysteine; L-methionine sulfoxide |
Instrument | impact II |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
---|---|---|---|
0 | 2024-11-07 02:41:40 | ID requested | |
⏵ 1 | 2025-01-24 05:19:14 | announced |
Publication List
no publication |
Keyword List
submitter keyword: antivenom, reverse antivenomics, affinity chromatography, DatasetType:Proteomics |
Contact List
Alexandre Keiji Tashima | |
---|---|
contact affiliation | Escola Paulista de Medicina/UNIFESP |
contact email | aktashima@unifesp.br |
lab head | |
Alexandre Keiji Tashima | |
contact affiliation | Universidade Federal de Sao Paulo |
contact email | aktashima@unifesp.br |
dataset submitter |
Full Dataset Link List
MassIVE dataset URI |
Dataset FTP location NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://massive.ucsd.edu/v07/MSV000096324/ |