Identification of the myotoxic site of the Lys49 phospholipase A(2) from Agkistrodon piscivorus piscivorus snake venom: synthetic C-terminal peptidesfrom Lys49, but not from Asp49 myotoxins, exert membrane-damaging activities

Group II phospholipase A, (PLA,) myotoxins found in the venoms of Crotalida e snakes can be divided into 'Asp49' and 'Lys49' isoforms, the latter being considered catalytically-inactive variants. Previous studies on one Lys49 isoform, myotoxin II from Bothrops asper, indicated that its myotoxic activ ity is due to the presence of a short cationic/hydrophobic sequence (115-12 9) near its C-terminus, which displays membrane-damaging properties. Since the C-terminal region of different group II PLA(2) myotoxins presents consi derable sequence variability, synthetic peptides homologous to region 115-1 29 of myotoxin II, but corresponding to B. asper myotoxin III (Asp49), Agki strodon piscivorus piscivorus Asp49 PLA, and Lys49 PLA2, were studied to de termine the possible functional relevance of such region for the toxic acti vities of these proteins. Results showed that both Lys49-derived peptides ( p-BaK49 and p-AppK49) were able to lyse skeletal muscle C2Cl2 cells in cult ure, and to induce edema in the mouse footpad assay. Moreover, p-AppK49, wh ich showed a markedly stronger cytotoxic potency than p-BaK49, additionally induced skeletal muscle necrosis when injected into mice. These observatio ns unequivocally identify the sequence 115-129 (KKYKAYFKLKCKK) of the Lys49 PLA(2) of A. p. piscivorus as containing the key structural determinants n eeded for myotoxicity, and represent the first report of an unmodified, PLA (2)-derived short synthetic peptide with the ability to reproduce this effe ct of a parent toxin in vivo. On the other hand, the two Asp49-derived pept ides did not show any toxic effects in vitro or in vivo, even at high conce ntrations. These findings suggests that Lys49 and Asp49 group II PLA(2)s mi ght exert their myotoxic actions through different molecular mechanisms, by implying that the latter may not utilize their C-terminal regions as main membrane-destabilizing elements. (C) 2001 Elsevier Science Ltd. All rights reserved.