Peptide fingerprinting of the neurotoxic fractions isolated from the secretions of sea anemones Stichodactyla helianthus and Bunodosoma granulifera. New members of the APETx-like family identified by a 454 pyrosequencing approach


Autoria(s): Alexei Rodriguez, Armando; Cassoli, Juliana Silva; Sa, Fei; Dong, Zhi Qiang; de Freitas, Jose Carlos; Pimenta, Adriano M. C.; de Lima, Maria Elena; Konnoe, Katsuhiro; Lee, Simon Ming Yuen; Garateix, Anoland; Zaharenko, Andre J.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

31/10/2013

31/10/2013

02/08/2013

Resumo

Sea anemones are known to contain a wide diversity of biologically active peptides, mostly unexplored according to recent peptidomic and transcriptomic studies. In the present work, the neurotoxic fractions from the exudates of Stichodactyla helianthus and Bunodosoma granulifera were analyzed by reversed-phase chromatography and mass spectrometry. The first peptide fingerprints of these sea anemones were assessed, revealing the largest number of peptide components (156) so far found in sea anemone species, as well as the richer peptide diversity of B. granulifera in relation to S. helianthus. The transcriptomic analysis of B. granulifera, performed by massive cDNA sequencing with 454 pyrosequencing approach allowed the discovery of five new APETx-like peptides (U-AITX-Bg1a-e - including the full sequences of their precursors for four of them), which together with type 1 sea anemone sodium channel toxins constitute a very distinguishable feature of studied sea anemone species belonging to genus Bunodosoma. The molecular modeling of these new APETx-like peptides showed a distribution of positively charged and aromatic residues in putative contact surfaces as observed in other animal toxins. On the other hand, they also showed variable electrostatic potentials, thus suggesting a docking onto their targeted channels in different spatial orientations. Moreover several crab paralyzing toxins (other than U-AITX-Bg1a-e), which induce a variety of symptoms in crabs, were isolated. Some of them presumably belong to new classes of crab-paralyzing peptide toxins, especially those with molecular masses below 2 kDa, which represent the smallest peptide toxins found in sea anemones. (C) 2011 Elsevier Inc. All rights reserved.

CNPqCITMA (Brazil)

CNPq-CITMA (Brazil) [490194/2007-9]

FAPESP [07/56525-3]

FAPESP

FAPEMIG

FAPEMIG

INCTTOX

INCTTOX

CAPES

CAPES

CNPq

CNPq

Science and Technology Development Fund of Macau SAR

Science and Technology Development Fund of Macau SAR [058/2009]

Research Committee, University of Macau [UL017/09-Y1]

Research Committee, University of Macau

International Foundation for Science [F/4082-1, F/4082-2]

International Foundation for Science

Third World Academy of Sciences [06344-2007]

Third World Academy of Sciences

Identificador

PEPTIDES, NEW YORK, v. 34, n. 1, Special Issue, supl. 1, Part 3, pp. 26-38, MAR, 2012

0196-9781

http://www.producao.usp.br/handle/BDPI/36992

10.1016/j.peptides.2011.10.011

http://dx.doi.org/10.1016/j.peptides.2011.10.011

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE INC

NEW YORK

Relação

PEPTIDES

Direitos

closedAccess

Copyright ELSEVIER SCIENCE INC

Palavras-Chave #SEA ANEMONE #PEPTIDE FINGERPRINT #PEPTIDOMICS #VENOM #TOXIN #TRANSCRIPTOMICS #454 SEQUENCING #STICHODACTYLA HELIANTHUS #BUNODOSOMA GRANULIFERA #POTASSIUM-CHANNEL TOXIN #AMINO-ACID-SEQUENCE #ANTHOPLEURA-ELEGANTISSIMA #SODIUM-CHANNEL #SNAKE VENOMICS #PROTEIN-STRUCTURE #PHARMACOLOGICAL PROPERTIES #TRANSCRIPTOME ANALYSIS #BIOLOGICAL-ACTIVITY #SWISS-MODEL #BIOCHEMISTRY & MOLECULAR BIOLOGY #PHARMACOLOGY & PHARMACY
Tipo

article

original article

publishedVersion