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Por favor, use este identificador para citar o enlazar a este item: http://hdl.handle.net/10261/164192
Título

PhcrTx2, a New Crab-Paralyzing Peptide Toxin from the Sea Anemone Phymanthus crucifer

AutorRodríguez, Armando Alexei; Garateix, Anoland; Salceda, Emilio; Peigneur, Steve; Zaharenko, André Junqueira; Pons, Tirso; Santos, Yúlica; Arreguín, Roberto; Ständker, Ludger; Forssmann, Wolf-Georg; Tytgat, Jan; Vega, Rosario; Soto, Enrique
Fecha de publicación7-feb-2018
EditorMultidisciplinary Digital Publishing Institute
CitaciónToxins 10 (2): 72 (2018)
ResumenSea anemones produce proteinaceous toxins for predation and defense, including peptide toxins that act on a large variety of ion channels of pharmacological and biomedical interest. <i>Phymanthus crucifer</i> is commonly found in the Caribbean Sea; however, the chemical structure and biological activity of its toxins remain unknown, with the exception of PhcrTx1, an acid-sensing ion channel (ASIC) inhibitor. Therefore, in the present work, we focused on the isolation and characterization of new <i>P. crucifer</i> toxins by chromatographic fractionation, followed by a toxicity screening on crabs, an evaluation of ion channels, and sequence analysis. Five groups of toxic chromatographic fractions were found, and a new paralyzing toxin was purified and named PhcrTx2. The toxin inhibited glutamate-gated currents in snail neurons (maximum inhibition of 35%, IC<sub>50</sub> 4.7 µM), and displayed little or no influence on voltage-sensitive sodium/potassium channels in snail and rat dorsal root ganglion (DRG) neurons, nor on a variety of cloned voltage-gated ion channels. The toxin sequence was fully elucidated by Edman degradation. PhcrTx2 is a new β-defensin-fold peptide that shares a sequence similarity to type 3 potassium channels toxins. However, its low activity on the evaluated ion channels suggests that its molecular target remains unknown. PhcrTx2 is the first known paralyzing toxin in the family Phymanthidae.
Versión del editorhttps://doi.org/10.3390/toxins10020072
URIhttp://hdl.handle.net/10261/164192
Identificadoresdoi: 10.3390/toxins10020072
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