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

THESIS

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

Quintero A^I; Soares AM^II

^IGraduate Program, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, USP, Ribeirão Preto, São Paulo State, Brazil

^IIDepartment of Clinical, Toxicological and Bromatological Analysis, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, USP, Ribeirão Preto, São Paulo State, Brazil

^{Correspondence to}

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 A₂, namely MTX-I, MTX-II, MTX-III, MTX-IV, and a new acid phospholipase A₂ called Basp-I-PLA₂. 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 NH₄HCO₃ 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 A₂. The acidic isoform demonstrated more catalytic activity than basic PLA₂s. 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-PLA₂. 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-PLA₂ = 14,246.0.8 Da. The PLA₂s (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 A₂, 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-PLA₂ belong to the subclass of Asp49 phospholipases A₂ catalytically active whereas MTX-II and MTX-IV belong to proteins of the subclass of the enzymatically inactive Lys49 PLA₂s-like. In addition, a sequence of the N-terminal region of the basic PLA₂ 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-PLA₂ is a new acidic PLA₂ and its N-terminal sequence revealed a high homology with other Asp49 acidic PLA₂s from snake venoms.

Key words:Bothrops asper, Panamá, snake venom characterization, phospholipases A₂, myotoxicity, inhibition of platelet aggregation, inflammation.

A. Quintero was advised by Professor Andreimar M. Soares, and submitted this thesis for his Doctorate in Toxicology at the School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, USP, Ribeirão Preto, São Paulo State, Brazil, 2009.

Publication Dates

• Publication in this collection
  30 Sept 2011
• Date of issue
  2010