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δ/ω-Plectoxin-Pt1a: An Excitatory Spider Toxin with Actions on both Ca2+ and Na+ Channels
Journal article   Open access   Peer reviewed

δ/ω-Plectoxin-Pt1a: An Excitatory Spider Toxin with Actions on both Ca2+ and Na+ Channels

Yi Zhou, Mingli Zhao, Gregg B Fields, Chun-Fang Wu and W. Dale Branton
PloS one, Vol.8(5), p.e64324
05/14/2013
DOI: 10.1371/journal.pone.0064324
PMCID: PMC3653879
PMID: 23691198
url
https://doi.org/10.1371/journal.pone.0064324View
Published (Version of record) Open Access

Abstract

The venom of spider Plectreurys tristis contains a variety of peptide toxins that selectively target neuronal ion channels. O-palmitoylation of a threonine or serine residue, along with a characteristic and highly constrained disulfide bond structure, are hallmarks of a family of toxins found in this venom. Here, we report the isolation and characterization of a new toxin, δ/ω-plectoxin-Pt1a, from this spider venom. It is a 40 amino acid peptide containing an O-palmitoylated Ser-39. Analysis of δ/ω-plectoxin-Pt1a cDNA reveals a small precursor containing a secretion signal sequence, a 14 amino acid N-terminal propeptide, and a C-terminal amidation signal. The biological activity of δ/ω-plectoxin-Pt1a is also unique. It preferentially blocks a subset of Ca 2+ channels that is apparently not required for neurotransmitter release; decreases threshold for Na + channel activation; and slows Na + channel inactivation. As δ/ω-plectoxin-Pt1a enhances synaptic transmission by prolonging presynaptic release of neurotransmitter, its effects on Na + and Ca 2+ channels may act synergistically to sustain the terminal excitability.
Biology

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