Vieira, Lara F.Magro, Angelo J.Fernandes, Carlos A.H.de Souza, Bibiana M.Cavalcante, Walter L.G.Palma, Mario Sergio [UNESP]Rosa, José C.Fuly, André L.Fontes, Marcos R.M.Gallacci, MárciaButzke, Diana S.Calderon, Leonardo A.Stábeli, Rodrigo G.Giglio, José R.Soares, Andreimar M.2014-05-272014-05-272013-09-26Biochimie.0300-90846183-1638http://hdl.handle.net/11449/76648Crotoxin is a neurotoxin from Crotalus durissus terrificus venom that shows immunomodulatory, anti-inflammatory, antimicrobial, antitumor and analgesic activities. Structurally, this toxin is a heterodimeric complex composed by a toxic basic PLA2 (Crotoxin B or CB) non-covalently linked to an atoxic non-enzymatic and acidic component (Crotapotin, Crotoxin A or CA). Several CA and CB isoforms have been isolated and characterized, showing that the crotoxin venom fraction is, in fact, a mixture of different molecules derived from the combination of distinct subunit isoforms. Intercro (IC) is a protein from the same snake venom which presents high similarity in primary structure to CB, indicating that it could be an another isoform of this toxin. In this work, we compare IC to the crotoxin complex (CA/CB) and/or CB in order to understand its functional aspects. The experiments with IC revealed that it is a new toxin with different biological activities from CB, keeping its catalytic activity but presenting low myotoxicity and absence of neurotoxic activity. The results also indicated that IC is structurally similar to CB isoforms, but probably it is not able to form a neurotoxic active complex with crotoxin A as observed for CB. Moreover, structural and phylogenetic data suggest that IC is a new toxin with possible toxic effects not related to the typical CB neurotoxin. © 2013.engCB isoformsCrotalus durissus terrificusIntercroOligomerizationPhospholipase A2Artigo10.1016/j.biochi.2013.08.028WOS:000327805400019Acesso restrito2-s2.0-8488449214629018886245065359353490382598257