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Hydra actinoporin-like toxin-1, an unusual hemolysin from the nematocyst venom of Hydra magnipapillata which belongs to an extended gene family.
Glasser, Eliezra; Rachamim, Tamar; Aharonovich, Dikla; Sher, Daniel.
Afiliação
  • Glasser E; Department of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, 31905 Haifa, Israel.
  • Rachamim T; Department of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, 31905 Haifa, Israel.
  • Aharonovich D; Department of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, 31905 Haifa, Israel.
  • Sher D; Department of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, 31905 Haifa, Israel. Electronic address: dsher@univ.haifa.ac.il.
Toxicon ; 91: 103-13, 2014 Dec.
Article em En | MEDLINE | ID: mdl-24768765
Cnidarians rely on their nematocysts and the venom injected through these unique weaponry systems to catch prey and protect themselves from predators. The development and physiology of the nematocysts of Hydra magnipapillata, a classic model organism, have been intensively studied, yet the composition and biochemical activity of their venom components are mostly unknown. Here, we show that hydra actinoporin-like toxins (HALTs), which have previously been associated with Hydra nematocysts, belong to a multigene family comprising six genes, which have diverged from a single common ancestor. All six genes are expressed in a population of Hydra magnipapillata. When expressed recombinantly, HALT-1 (Δ-HYTX-Hma1a), an actinoporin-like protein found in the stenoteles (the main penetrating nematocysts used in prey capture), reveals hemolytic activity, albeit about two-thirds lower than that of the anemone actinoporin equinatoxin II (EqTII, Δ-AITX-Aeq1a). HALT-1 also differs from EqTII in the size of its pores, and likely does not utilize sphingomyelin as a membrane receptor. We describe features of the HALT-1 sequence which may contribute to this difference in activity, and speculate on the role of this unusual family of pore-forming toxins in the ecology of Hydra.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Família Multigênica / Proteínas Hemolisinas / Hydra / Toxinas Marinhas Limite: Animals Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Família Multigênica / Proteínas Hemolisinas / Hydra / Toxinas Marinhas Limite: Animals Idioma: En Ano de publicação: 2014 Tipo de documento: Article