Please use this identifier to cite or link to this item: https://repository.ucc.edu.co/handle/20.500.12494/42681
Title: Isolation and functional characterization of a basic phospholipase A2 from Colombian Bothrops asper venom
Author: Pereañez J.A.
Quintana Castillo, Juan Carlos
Alarcón J.C.
Núñez V.
Email autor: juan.quintanac@campusucc.edu.co
Issue Date: 2014
Keywords: myotoxin
phospholipase A2
snake venom
unclassified drug
animal cell
animal experiment
anticoagulation
article
biological activity
Bothrops
controlled study
creatine kinase blood level
cytotoxicity
foot edema
foot pad
ion exchange chromatography
mass spectrometry
mouse
myoblast
myotube
nonhuman
nucleotide sequence
polyacrylamide gel electrophoresis
protein analysis
protein purification
reversed phase high performance liquid chromatography
skeletal muscle
Abstract: Background: Snakebites represent a relevant public health issue in many regions of the world, particularly in tropical and subtropical countries of Africa, Asia, Latin America and Oceania. Snake venoms are complex mixtures of toxic enzymes and proteins, where the most important and abundant muscle-damaging components in snake venoms are phospholipases A2 (PLA2s). Objective: Isolate and characterize a phospholipase A2 from Colombian Bothrops asper venom, in order to obtain information about venom composition of this species. Materials and methods: Cation-exchange chromatography followed by reverse phase HPLC were used to purify the protein. Mass spectrometry was used to determine its molecular mass. Biochemical characterization was performed using a synthetic substrate (4-nitro-3-octanoyloxy-benzoic acid). Myotoxic and edema-inducing activity of toxin were tested in mice, by measuring the plasma creatine kinase activity and footpad diameter, respectively. Moreover, cytotoxic activity was examined to murine skeletal muscle C2C12 myoblasts and myotubes. Results: A PLA2 of Bothrops asper venom from Colombia (BaspCol-PLA2) was purified. Its molecular mass was 13974.6 Da. The enzyme hydrolyzed a synthetic substrate with a KM of 3.11 mM and a VMax of 4.47 nmol/min, showing maximum activity at 40 °C and at pH 8.0. The PLA2 required Ca2+ for activity. The addition of Mg2+, Cd2+, Mn2+ and Zn2+ (10mM) in the presence of low Ca2+ concentration (1mM) decreased the enzyme activity. The substitution of Ca2+ by mentioned divalent cations also reduced the activity to levels similar to those in the absence of Ca2+. Three internal fragments (CCFVHDCCYGK, AAAI/ LCFRDNI/LNTYNDKK, DAAI/LCFR) identified by a mass spectrometry analysis showed similarity with previously reported B. asper PLA2s. In mice, BaspCol-PLA2 induced a conspicuous local myotoxic effect and moderate footpad edema. In vitro, this enzyme induced cytotoxic effect on both myoblasts and myotubes. Additionally, it was classified as weakly anticoagulant PLA2, showing this effect at concentrations between 3 and 10 µg/mL when using human plasma. Conclusions: A PLA2 was purified and named BaspCol-PLA2, this enzyme displayed catalytic activity and molecular mass of 13974.6 Da. The toxin showed myotoxic, edema-forming, anticoagulant and cytotoxic activities.
Publisher: Universidad de Antioquia
metadata.dc.type: Artículo
Citation: Pereañez JA,Quintana JC,Alarcón JC,Núñez V. Isolation and functional characterization of a basic phospholipase A2 from Colombian Bothrops asper venom. Vitae. 2014. 21. (1):p. 38-48. .
Other Identifiers: https://www.scielo.org.co/pdf/vitae/v21n1/v21n1a5.pdf
Appears in Collections:Artículos Científicos

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