Proteomics of the neurotoxic fraction from the sea anemone Bunodosoma cangicum venom: Novel peptides belonging to new classes of toxins


Autoria(s): ZAHARENKO, Andre Junqueira; FERREIRA JR., Wilson Alves; OLIVEIRA, Joacir Stolarz; RICHARDSON, Michael; PIMENTA, Daniel Carvalho; KONNO, Katsuhiro; PORTARO, Fernanda C. V.; FREITAS, Jose Carlos de
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2008

Resumo

In contrast to the many studies on the venoms of scorpions, spiders, snakes and cone snails, tip to now there has been no report of the proteomic analysis of sea anemones venoms. In this work we report for the first time the peptide mass fingerprint and some novel peptides in the neurotoxic fraction (Fr III) of the sea anemone Bunodosoma cangicum venom. Fr III is neurotoxic to crabs and was purified by rp-HPLC in a C-18 column, yielding 41 fractions. By checking their molecular masses by ESI-Q-Tof and MALDI-Tof MS we found 81 components ranging from near 250 amu to approximately 6000 amu. Some of the peptidic molecules were partially sequenced through the automated Edman technique. Three of them are peptides with near 4500 amu belonging to the class of the BcIV, BDS-I, BDS-II, APETx1, APETx2 and Am-II toxins. Another three peptides represent a novel group of toxins (similar to 3200 amu). A further three molecules (similar to similar to 4900 amu) belong to the group of type 1 sodium channel neurotoxins. When assayed over the crab leg nerve compound action potentials, one of the BcIV- and APETx-like peptides exhibits an action similar to the type 1 sodium channel toxins in this preparation, suggesting the same target in this assay. On the other hand one of the novel peptides, with 3176 amu, displayed an action similar to potassium channel blockage in this experiment. In summary, the proteomic analysis and mass fingerprint of fractions from sea anemone venoms through MS are valuable tools, allowing us to rapidly predict the occurrence of different groups of toxins and facilitating the search and characterization of novel molecules without the need of full characterization of individual components by broader assays and bioassay-guided purifications. It also shows that sea anemones employ dozens of components for prey capture and defense. (C) 2008 Elsevier Inc. All rights reserved.

CNPq[563874/2005-8]

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

FAPESP[01/14243-5]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

CAT/CEPID

Identificador

COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY D-GENOMICS & PROTEOMICS, v.3, n.3, p.219-225, 2008

1744-117X

http://producao.usp.br/handle/BDPI/27454

10.1016/j.cbd.2008.04.002

http://dx.doi.org/10.1016/j.cbd.2008.04.002

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE INC

Relação

Comparative Biochemistry and Physiology D-genomics & Proteomics

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE INC

Palavras-Chave #Bunodosoma cangicum #sea anemone #mass spectrometry #peptide mass fingerprint #HPLC #neurotoxins #ion channels #AMINO-ACID-SEQUENCE #TIME-OF-FLIGHT #CARDIAC SODIUM-CHANNELS #MASS-SPECTROMETRY #ANTHOPLEURA-ELEGANTISSIMA #ACTINIA-EQUINA #SNAKE-VENOMS #SPIDER VENOM #K+-CHANNELS #IDENTIFICATION #Biochemistry & Molecular Biology #Genetics & Heredity
Tipo

article

original article

publishedVersion