Two Toxins from Conus striatus That Individually Induce Tetanic Paralysis

Wayne P. Kelley,§ Joseph R. Schulz, Jennifer A. Jakubowski, William F. Gilly, and Jonathan V. Sweedler*
Department of Chemistry and The Beckman Institute for Advanced Science and Technology, University of Illinois at UrbanaChampaign, Urbana, Illinois 61801, and Hopkins Marine Station of Stanford University, Department of Biological Sciences, Pacific Grove, California 93950
Biochemistry, 2006, 45 (47), pp 14212–14222
DOI: 10.1021/bi061485s
Publication Date (Web): November 3, 2006
Copyright © 2006 American Chemical Society

 This work was supported by NIH Grant NS 31609 and NSF Grant CHE 04-00768 (to J.V.S.), Kirschstein NRSA 5F32NS43938 (to J.R.S.), NSF Grant IBN 0131788 (to W.F.G.), and a fellowship from Merck Research Laboratories (to J.A.J.).

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 University of Illinois at Urbana−Champaign.

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§

 Current address:  Pharmaceutical Development, GlaxoSmithKline, 709 Swedeland Road, King of Prussia, PA 19406.

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 Stanford University.

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 Current address:  Occidental College, Los Angeles, CA 90041.

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*

 Corresponding author. E-mail:  sweedler@scs.uiuc.edu. Tel:  (217) 244-7359. Fax:  (217) 244-8068.

Abstract

Abstract Image

We describe structural properties and biological activities of two related O-glycosylated peptide toxins isolated from injected (milked) venom of Conus striatus, a piscivorous snail that captures prey by injecting a venom that induces a violent, spastic paralysis. One 30 amino acid toxin is identified as κA-SIVA (termed s4a here), and another 37 amino acid toxin, s4b, corresponds to a putative peptide encoded by a previously reported cDNA. We confirm the amino acid sequences and carry out structural analyses of both mature toxins using multiple mass spectrometric techniques. These include electrospray ionization ion-trap mass spectrometry and nanoelectrospray techniques for small volume samples, as well as matrix-assisted laser desorption/ionization time of flight mass spectrometric analysis as a complementary method to assist in the determination of posttranslational modifications, including O-linked glycosylation. Physiological experiments indicate that both s4a and s4b induce intense repetitive firing of the frog neuromuscular junction, leading to a tetanic contracture in muscle fiber. These effects apparently involve modification of voltage-gated sodium channels in motor axons. Notably, application of either s4a or s4b alone mimics the biological effects of the whole injected venom on fish prey.

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History

  • Published In Issue November 28, 2006
  • Received July 21, 2006
    Revised Manuscript Received September 20, 2006

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