Abstract
Boiga dendrophila (mangrove catsnake) is a colubrid snake that lives in Southeast Asian lowland rainforests and mangrove swamps and that preys primarily on birds. We have isolated, purified, and sequenced a novel toxin from its venom, which we named denmotoxin. It is a monomeric polypeptide of 77 amino acid residues with five disulfide bridges. In organ bath experiments, it displayed potent postsynaptic neuromuscular activity and irreversibly inhibited indirectly stimulated twitches in chick biventer cervicis nerve-muscle preparations. In contrast, it induced much smaller and readily reversible inhibition of electrically induced twitches in mouse hemidiaphragm nerve-muscle preparations. More precisely, the chick muscle alpha(1)betagammadelta-nicotinic acetylcholine receptor was 100-fold more susceptible compared with the mouse receptor. These data indicate that denmotoxin has a bird-specific postsynaptic activity. We chemically synthesized denmotoxin, crystallized it, and solved its crystal structure at 1.9 A by the molecular replacement method. The toxin structure adopts a non-conventional three-finger fold with an additional (fifth) disulfide bond in the first loop and seven additional residues at its N terminus, which is blocked by a pyroglutamic acid residue. This is the first crystal structure of a three-finger toxin from colubrid snake venom and the first fully characterized bird-specific toxin. Denmotoxin illustrates the relationship between toxin specificity and the primary prey type that constitutes the snake's diet.
Highlights
Three-finger toxins (3FTXs)3 form one of the most abundant, well recognized families of snake venom proteins
We report the isolation, purification, and pharmacological and structural characterization of a novel bird-specific neurotoxin, denmotoxin, one of the major venom components of the mangrove catsnake (Boiga dendrophila)
Pharmacological studies revealed that denmotoxin is a taxon-specific postsynaptic neurotoxin
Summary
Materials—Most chemicals and drugs (including carbamylcholine chloride, d-tubocurarine chloride, and neostigmine bromide) were purchased from Sigma. The pooled fractions containing the protein of interest were applied to an RP-Jupiter C18 HPLC column using the same chromatography system and eluted with a linear gradient of 30 – 40% solvent B over 80 min (solvent A ϭ 0.1% trifluoroacetic acid in H2O and solvent B ϭ 80% acetonitrile and 0.1% trifluoroacetic acid in H2O). The protein was confirmed to be a monomer by gel filtration chromatography (Fig. 1E), as only one peak eluted at a retention time of 73 min, corresponding to a mass of ϳ8 kDa (monomeric) We named this protein denmotoxin for B. dendrophila monomeric toxin
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