Cloning and activity of a novel alpha-latrotoxin from red-back spider venom

Andis Graudins, Michelle Little, Sandy S Pineda, Peter G Hains, Glenn F King, Kevin Broady, Graham Michael Nicholson

Research output: Contribution to journalArticleResearchpeer-review

28 Citations (Scopus)


The venom of the European black widow spider Latrodectus tredecimguttatus (Theridiidae) contains several high molecular mass (110-140 kDa) neurotoxins that induce neurotransmitter exocytosis. These include a vertebrate-specific alpha-latrotoxin (alpha-LTX-Lt1a) responsible for the clinical symptoms of latrodectism and numerous insect-specific latroinsectoxins (LITs). In contrast, little is known about the expression of these toxins in other Latrodectus species despite the fact that envenomation by these spiders induces a similar clinical syndrome. Here we report highly conserved alpha-LTX, alpha-LIT and delta-LIT sequence tags in Latrodectus mactans, Latrodectus hesperus and Latrodectus hasselti venoms using tandem mass spectrometry, following bioassay-guided separation of venoms by liquid chromatography. Despite this sequence similarity, we show that the anti-alpha-LTX monoclonal antibody 4C4.1, raised against alpha-LTX-Lt1a, fails to neutralize the neurotoxicity of all other Latrodectus venoms tested in an isolated chick biventer cervicis nerve-muscle bioassay. This suggests that there are important structural differences between alpha-LTXs in theridiid spider venoms. We therefore cloned and sequenced the alpha-LTX from the Australian red-back spider L. hasselti (alpha-LTX-Lh1a). The deduced amino acid sequence of the mature alpha-LTX-Lh1a comprises 1180 residues ( approximately 132kDa) with approximately 93 sequence identity with alpha-LTX-Lt1a. alpha-LTX-Lh1a is composed of an N-terminal domain and a central region containing 22 ankyrin-like repeats. The presence of two furin cleavage sites, conserved with alpha-LTX-Lt1a, indicates that alpha-LTX-Lh1a is derived from the proteolytic cleavage of an N-terminal signal peptide and C-terminal propeptide region. However, we show that alpha-LTX-Lh1a has key substitutions in the 4C4.1 epitope that explains the lack of binding of the monoclonal antibody.
Original languageEnglish
Pages (from-to)170 - 183
Number of pages14
JournalBiochemical Pharmacology
Issue number1
Publication statusPublished - 2012

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