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Agkistrodon piscivorus venom toxins represent the complex mixture of bioactive proteins and peptides found in the venom of the North American cottonmouth snake. The venom is primarily composed of zinc-dependent metalloproteinases (SVMPs), phospholipases A2 (PLA2s), and serine proteinases (SVSPs), which work synergistically to immobilize prey and initiate digestion [1][2]. SVMPs are largely responsible for local tissue destruction and hemorrhage by degrading basement membrane proteins, while PLA2s contribute to severe myotoxicity and inflammation by disrupting cell membranes [3]. Additionally, the venom contains disintegrins and C-type lectins that interfere with platelet function, and L-amino acid oxidases that induce oxidative stress and cytotoxicity [4]. From a therapeutic perspective, these toxins are the primary targets for antivenoms like CroFab and Anavip, which utilize purified antibodies to neutralize the enzymatic activity and prevent systemic toxicity [5]. Beyond envenomation treatment, specific toxins such as the disintegrin applaggin have been researched as templates for developing anti-platelet and anti-cancer therapeutics [6].
Neutralization of venom enzymes and toxins through antibody binding (Fab or F(ab')2 fragments) to prevent interaction with host tissues and substrates.
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