Purification and amino acid sequence of MP-III 4R D49 phospholipase A2 from Bothrops pirajai snake venom, a toxin with moderate PLA2 and anticoagulant activities and high myotoxic activity

MP-III 4R PLA2 was purified from the venom of Bothrops pirajai venom (Bahia's jararacussu) after three chromatographic steps which started with RP-HPLC. The complete amino acid sequence of MP-III 4R PLA2 from Bothrops pirajai was determined by amino acid sequencing of reduced and carboxymethyla...

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Published in:Journal of Protein Chemistry Vol. 18; no. 3; pp. 371 - 378
Main Authors: Toyama, M H, Costa, P D, Novello, J C, de Oliveira, B, Giglio, J R, da Cruz-Höfling, M A, Marangoni, S
Format: Journal Article
Language:English
Published: United States Springer Nature B.V 01-04-1999
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Abstract MP-III 4R PLA2 was purified from the venom of Bothrops pirajai venom (Bahia's jararacussu) after three chromatographic steps which started with RP-HPLC. The complete amino acid sequence of MP-III 4R PLA2 from Bothrops pirajai was determined by amino acid sequencing of reduced and carboxymethylated MP-III 4R and the isolated peptides from clostripain and protease V8 digestion. MP-III 4R is a D49 PLA2 with 121 amino acid residues and has a molecular weight estimated at 13,800 Da, with 14 half-cysteines. This protein showed moderate PLA2 and anticoagulant activity. This PLA2 does not have a high degree of homology with other bothropic PLA2-like myotoxins (approximately 75%) and nonbothropic myotoxins (approximately 60%). MP-III 4R is a new PLA2, which was isolated using exclusively analytical and preparative HPLC methods. Based on the N-terminal sequence and biological activities, MP-III 4R was identified as similar to piratoxin-III (PrTX-III), which was isolated by conventional chromatography based on molecular exclusion ion exchange chromatography. Clinical manifestations indicate that at the site of toxin injection, there may be pain of variable intensity, because animals continue to lick the limb. No clinical sign indicating general toxicity was noticed. Myotoxicity was observed in gastrocnemius muscle cells after exposure to MP-III 4R, with a high frequency (70%) of affected muscle fibers.
AbstractList MP-III 4R PLA2 was purified from the venom of Bothrops pirajai venom (Bahia's jararacussu) after three chromatographic steps which started with RP-HPLC. The complete amino acid sequence of MP-III 4R PLA2 from Bothrops pirajai was determined by amino acid sequencing of reduced and carboxymethylated MP-III 4R and the isolated peptides from clostripain and protease V8 digestion. MP-III 4R is a D49 PLA2 with 121 amino acid residues and has a molecular weight estimated at 13,800 Da, with 14 half-cysteines. This protein showed moderate PLA2 and anticoagulant activity. This PLA2 does not have a high degree of homology with other bothropic PLA2-like myotoxins (approximately 75%) and nonbothropic myotoxins (approximately 60%). MP-III 4R is a new PLA2, which was isolated using exclusively analytical and preparative HPLC methods. Based on the N-terminal sequence and biological activities, MP-III 4R was identified as similar to piratoxin-III (PrTX-III), which was isolated by conventional chromatography based on molecular exclusion ion exchange chromatography. Clinical manifestations indicate that at the site of toxin injection, there may be pain of variable intensity, because animals continue to lick the limb. No clinical sign indicating general toxicity was noticed. Myotoxicity was observed in gastrocnemius muscle cells after exposure to MP-III 4R, with a high frequency (70%) of affected muscle fibers.
MP-III 4R PLA2 was purified from the venom of Bothrops pirajai venom (Bahia's jararacussu) after three chromatographic steps which started with RP-HPLC. The complete amino acid sequence of MP-III 4R PLA2from Bothrops pirajai was determined by amino acid sequencing of reduced and carboxymethylated MP-III 4R and the isolated peptides from clostripain and protease V8 digestion. MP-III 4R is a D49 PLA2 with 121 amino acid residues and has a molecular weight estimated at 13,800 Da, with 14 half-cysteines. This protein showed moderate PLA2 and anticoagulant activity. This PLA2 does not have a high degree of homology with other bothropic PLA2-like myotoxins (~75%) and nonbothropic myotoxins (~60%). MP-III 4R is a new PLA2, which was isolated using exclusively analytical and preparative HPLC methods. Based on the N-terminal sequence and biological activities, MP-III 4R was identified as similar to piratoxin-III (PrTX-III), which was isolated by conventional chromatography based on molecular exclusion ion exchange chromatography. Clinical manifestations indicate that at the site of toxin injection, there may be pain of variable intensity, because animals continue to lick the limb. No clinical sign indicating general toxicity was noticed. Myotoxicity was observed in gastrocnemius muscle cells after exposure to MP-III 4R, with a high frequency (70%) of affected muscle fibers.
Author da Cruz-Höfling, M A
Novello, J C
Giglio, J R
Marangoni, S
de Oliveira, B
Toyama, M H
Costa, P D
Author_xml – sequence: 1
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  surname: Toyama
  fullname: Toyama, M H
  organization: Departamento do Bioquímica, Instituto de Biologia, UNICAMP, São Paulo, Brazil
– sequence: 2
  givenname: P D
  surname: Costa
  fullname: Costa, P D
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  givenname: J C
  surname: Novello
  fullname: Novello, J C
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  surname: de Oliveira
  fullname: de Oliveira, B
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  surname: Giglio
  fullname: Giglio, J R
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  surname: da Cruz-Höfling
  fullname: da Cruz-Höfling, M A
– sequence: 7
  givenname: S
  surname: Marangoni
  fullname: Marangoni, S
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Snippet MP-III 4R PLA2 was purified from the venom of Bothrops pirajai venom (Bahia's jararacussu) after three chromatographic steps which started with RP-HPLC. The...
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SubjectTerms Amino Acid Sequence
Amino acids
Animals
Anticoagulants
Anticoagulants - chemistry
Bothrops - metabolism
Bothrops pirajai
Chromatography, High Pressure Liquid
Chromatography, Ion Exchange
Clostripain
Gastrocnemius muscle
Group II Phospholipases A2
High performance liquid chromatography
Homology
Ion exchange
Liquid chromatography
Mice
Molecular Sequence Data
Molecular weight
Muscle, Skeletal - chemistry
Muscle, Skeletal - cytology
Muscles
Myotoxins
Peptides
Peptides - metabolism
Phospholipase A2
Phospholipases A - chemistry
Phospholipases A - isolation & purification
Phospholipases A2
Reptilian Proteins
Sequence Analysis
Sequence Homology, Amino Acid
Snake Venoms - chemistry
Snake Venoms - toxicity
Time Factors
Toxicity
Toxicology
Toxins
Toxins, Biological - chemistry
Venom
Viper Venoms
Title Purification and amino acid sequence of MP-III 4R D49 phospholipase A2 from Bothrops pirajai snake venom, a toxin with moderate PLA2 and anticoagulant activities and high myotoxic activity
URI https://www.ncbi.nlm.nih.gov/pubmed/10395455
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