Literature DB >> 11072049

Isolation and characterisation of five neurotoxic and cardiotoxic polypeptides from the sea anemone Anthopleura elegantissima.

T Bruhn1, C Schaller, C Schulze, J Sanchez-Rodriguez, C Dannmeier, U Ravens, J F Heubach, K Eckhardt, J Schmidtmayer, H Schmidt, A Aneiros, E Wachter, L Béress.   

Abstract

Five toxins (APE 1 to APE 5) of the sea anemone species Anthopleura elegantissima (Brandt) have been isolated from a toxic by-product fraction of its concentrated crude watery-methanolic extract, prepared previously for the isolation of a neuropeptide (the head-activator) by Schaller and Bodenmüller (Proc. Natl. Acad. Sci. USA 78 (1981) 7000) from 200kg sea anemones. Toxin purification was performed by desalting of the starting material by dialysis (MWCO 3500) against distilled water, anion exchange chromatography on QAE-Sephadex A25 at pH 8, twice gel filtration on Sephadex G50 m, repeated chromatography on QAE-Sephadex at pH 10 and chromatography on the cation exchanger Fractogel EMD SO(3)(-)-650 M.Final purification of the toxins was achieved by HPLC on MN SP 250/10 Nucleosil 500-5 C(18) PPN and MN SP 250/21 Nucleosil 300-7 C(18). Each toxin was composed of at least two isotoxins of which APE 1-1, APE 1-2, APE 2-1, APE 2-2 and APE 5-3 were isolated in preparative scale. With exception of APE 5-3 the sequences of the isotoxins have been elucidated. They resemble the 47 residue type-I long polypeptide toxins native to Anemonia sulcata (Pennant). All isotoxins paralyse the shore crab (Carcinus maenas) by tetanic contractions after i.m. application. The toxins modify current passing through the fast Na(+) channel in neuroblastoma cells, leading to delayed and incomplete inactivation. APE 1-1, APE 2-1 and APE 5-3 produce a positive inotropic effect in mammalian heart muscle, although they differ in potency. The order of potency is APE 2-1>APE 1-1>APE 5-3 (i.e. threshold concentrations are 1, 10 and 300nM, respectively). In addition, they enhance the spontaneous beating frequency in isolated right atria (guinea pig). The most potent cardiotoxic isotoxin is APE 2-1, its sequence is identical with that of AP-C, a toxin isolated and characterised previously by Norton et al. (Drugs and Foods from the Sea, 1978, University of Oklahoma Press, p. 37-50).LD50 APE 2-1:1 micro g/kg b.w. C. maenas (i.m.). LD50 APE 1-1:10 microg/kg b.w. C. maenas (i. m.). LD50 APE 5-3:50 microg/kg b.w. C. maenas (i.m.).

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Year:  2001        PMID: 11072049     DOI: 10.1016/s0041-0101(00)00199-9

Source DB:  PubMed          Journal:  Toxicon        ISSN: 0041-0101            Impact factor:   3.033


  20 in total

1.  Characterization of two Bunodosoma granulifera toxins active on cardiac sodium channels.

Authors:  C Goudet; T Ferrer; L Galàn; A Artiles; C F Batista; L D Possani; J Alvarez; A Aneiros; J Tytgat
Journal:  Br J Pharmacol       Date:  2001-11       Impact factor: 8.739

2.  A new sea anemone peptide, APETx2, inhibits ASIC3, a major acid-sensitive channel in sensory neurons.

Authors:  Sylvie Diochot; Anne Baron; Lachlan D Rash; Emmanuel Deval; Pierre Escoubas; Sabine Scarzello; Miguel Salinas; Michel Lazdunski
Journal:  EMBO J       Date:  2004-03-25       Impact factor: 11.598

3.  The effect of recombinant neurotoxins from the sea anemone Anthopleura sp. on sodium currents of rat cerebral cortical neurons.

Authors:  Hui Xiang; Wucheng Tao; Lei Wang; Fang Wang; Anlong Xu
Journal:  Cell Mol Neurobiol       Date:  2008-06-26       Impact factor: 5.046

4.  Neurotoxin localization to ectodermal gland cells uncovers an alternative mechanism of venom delivery in sea anemones.

Authors:  Yehu Moran; Grigory Genikhovich; Dalia Gordon; Stefanie Wienkoop; Claudia Zenkert; Suat Ozbek; Ulrich Technau; Michael Gurevitz
Journal:  Proc Biol Sci       Date:  2011-11-02       Impact factor: 5.349

Review 5.  Sea anemone (Cnidaria, Anthozoa, Actiniaria) toxins: an overview.

Authors:  Bárbara Frazão; Vitor Vasconcelos; Agostinho Antunes
Journal:  Mar Drugs       Date:  2012-08-22       Impact factor: 6.085

6.  Analgesic and antibutyrylcholinestrasic activities of the venom prepared from the Mediterranean jellyfish Pelagia noctiluca (Forsskal, 1775).

Authors:  Yosra Ayed; Afef Dellai; Hedi Ben Mansour; Hassen Bacha; Salwa Abid
Journal:  Ann Clin Microbiol Antimicrob       Date:  2012-06-12       Impact factor: 3.944

7.  Induction of cytotoxicity of Pelagia noctiluca venom causes reactive oxygen species generation, lipid peroxydation induction and DNA damage in human colon cancer cells.

Authors:  Yosra Ayed; Manel Boussabbeh; Wiem Zakhama; Chayma Bouaziz; Salwa Abid; Hassen Bacha
Journal:  Lipids Health Dis       Date:  2011-12-09       Impact factor: 3.876

8.  A RNA-seq approach to identify putative toxins from acrorhagi in aggressive and non-aggressive Anthopleura elegantissima polyps.

Authors:  Jason Macrander; Mercer R Brugler; Marymegan Daly
Journal:  BMC Genomics       Date:  2015-03-21       Impact factor: 3.969

9.  Analysis of soluble protein contents from the nematocysts of a model sea anemone sheds light on venom evolution.

Authors:  Yehu Moran; Daniela Praher; Ami Schlesinger; Ari Ayalon; Yossi Tal; Ulrich Technau
Journal:  Mar Biotechnol (NY)       Date:  2012-11-15       Impact factor: 3.619

10.  Preliminary results of the in vivo and in vitro characterization of a tentacle venom fraction from the jellyfish Aurelia aurita.

Authors:  Dalia Ponce; Estuardo López-Vera; Manuel B Aguilar; Judith Sánchez-Rodríguez
Journal:  Toxins (Basel)       Date:  2013-12-06       Impact factor: 4.546

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