Functional and structural characterization of phospholipases A² isolated from Bothrops asper snake venom in Panamá

Abstract

Abstract:Envenoming by Bothrops snakes is the most serious type of envenoming from the medical and economic point of view in Central America. Bothrops asper is responsible for 90% of the snakebites registered in Panamá every year. Despite its medical and economic relevance, only the venom of Costa Rican and Guatemalan populations of this species has been studied to some detail, and there is very little information on intraspecies variability in venom composition and toxicity. In this study the crude venom of B. asper from Panamá was characterized and its pharmacological and biochemistry activities were investigated with standard laboratory assays. Furthermore, we described the isolation, functional and structural characterization of four basic phospholipases A 2 , namely MTX-I, MTX-II, MTX-III, MTX-IV, and a new acid phospholipase A 2 called Basp-I-PLA 2 . The proteins were isolated from the crude venom by a combination of two chromatographic steps, using ion-exchange chromatography on CM-Sepharose (0.05 M NH 4 HCO 3 pH 8.1 buffer), and hydrophobic chromatography on Phenyl-Sepharose (0.05 M Tris-HCl pH 7.4), followed by concentration gradient from 4 to 0 M NaCl at 25°C in the same buffer. Analyses of phospholipids hydrolyzed by these enzymes have shown that all phospholipases belong to type A 2 . The acidic isoform demonstrated more catalytic activity than basic PLA 2 s. This enzyme was more active on substrates such as phosphotidylcholine and phosphatidylglycerol. The isoelectric focusing evidenced pIs between 8.1 to 8.3 for MTXs and 4.6 for the isoform Basp-I-PLA 2 . The molecular weight was estimated by mass spectrometry to be: MTX-1 = 14,156.5; MTX-2 = 14,249.5 and MTX-3 = 14,253.0 and Basp-I-PLA 2 = 14,246.0.8 Da. The PLA 2 s (MTX-I, II, III and IV) induced myotoxic activity, inflammatory reaction (mainly leukocyte migration to the muscle) and activation of macrophages to exert phagocytic activity and production of superoxide. MTX-II, the most abundant one, showed to be cytotoxic against JURKAT tumor cell line, C. albicans and E. coli. The acidic phospholipases A 2 , when tested in platelet rich plasma, showed a potent inhibitory effect on aggregation induced by ADP and collagen. The analysis of the N-terminal sequence demonstrated that MTX-I, MTX-III and BASP-I-PLA 2 belong to the subclass of Asp49 phospholipases A 2 catalytically active whereas MTX-II and MTX-IV belong to proteins of the subclass of the enzymatically inactive Lys49 PLA 2 s-like. In addition, a sequence of the N-terminal region of the basic PLA 2 isolated demonstrated clearly that isolated myotoxins in this work are similar to previously isolated myotoxins of Bothrops asper snake venom from Costa Rica. The Basp-I-PLA 2 is a new acidic PLA 2 and its N-terminal sequence revealed a high homology with other Asp49 acidic PLA 2 s from snake venoms.

Rastreamento em células in vitro de uma fosfolipase A2 da peçonha de Bothrops alternatus por meio de pontos quânticos de tamanhos mágicos

“…Our results showed that the enzyme has a high purity and has a molecular mass of 14,074.74 Da (Figure 3). The molecular mass of BaltPLA 2 is similar to other bothropic PLA 2 , such as MTX (I-III) [35], BLK-PLA 2 and BLD-PLA 2 [36] and BmarPLA 2 [37]. Fragments of ions were used to determine an internal amino acid sequence of BaltPLA 2 (SGVIICGEGTPCEK), which exhibited 100% identity with other bothropic PLA 2 s, as well as PLA 2 s from genera Sistrurus and Crotalus (Figure 4).…”