Busca avançada
Ano de início
Entree
(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Biochemical and pharmacological characterization of PhTX-I a new myotoxic phospholipase A(2) isolated from Porthidium hyoprora snake venom

Texto completo
Autor(es):
Huancahuire-Vega, Salomon [1] ; Ponce-Soto, Luis Alberto [1] ; Martins-de-Souza, Daniel [2] ; Marangoni, Sergio [1]
Número total de Autores: 4
Afiliação do(s) autor(es):
[1] State Univ Campinas UNICAMP, Dept Biochem, Inst Biol, BR-13083970 Campinas, SP - Brazil
[2] Max Planck Inst Psychiat, D-80804 Munich - Germany
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY; v. 154, n. 2, p. 108-119, AUG 2011.
Citações Web of Science: 10
Resumo

This paper reports the biochemical and pharmacological characterization of a new myotoxic PLA(2) (EC 3.1.1.4) called PhTX-I, purified from Porthidium hyoprora venom by one step analytical chromatography reverse phase HPLC. The homogeneity of the PhTX-I fraction and its molecular mass were initially evaluated by SDS-PAGE and confirmed by MALDI-TOF spectrometry, indicating a molecular mass of 14.249 Da and constituted of a single polipeptidic chain. Amino acid sequence was determined by ``de novo sequencing,{''} in tandem mass spectrometry, belonging to D49-PIA(2) enzyme class and exhibiting high identity (44-90%) with other myotoxics PLA(2) from snake venoms. The enzymatic investigation showed maximal activity at pH 8 and 35-45 degrees C. This activity was dependent on Ca(2+), other cations (Mg(2+), Mn(2+), Cd(2+) and Zn(2+)) reduced notably the enzymatic activity, suggesting that the arrangement of the catalytic site presents an exclusive structure for Ca(2+). Ex vivo, whole venom and PhTX-I PLA(2) caused blockade of the neuromuscular transmission in young chick biventer cervicis preparations similar to other isolated snake venom toxins from the Bothrops genus. In vivo, both induced local myotoxicity and systemic interleukin-6 response upon intramuscular injection, additionally, induced moderate footpad edema. In vitro, both induced low cytotoxicity in skeletal muscle myoblasts, however PhTX-I PLA(2) was able to lyse myotubes. (C) 2011 Elsevier Inc. All rights reserved. (AU)

Processo FAPESP: 09/51207-9 - Avaliacao das atividades miotoxica, neurotoxica, citotoxica e inflamatoria induzidas por miotoxinas e neurotoxinas fosfolipase a2 isoladas de veneno de porthidium hyoprora
Beneficiário:Salomon Huancahuire Vega
Modalidade de apoio: Bolsas no Brasil - Doutorado