Literature DB >> 21959992

Venom peptide analysis of Vipera ammodytes meridionalis (Viperinae) and Bothrops jararacussu (Crotalinae) demonstrates subfamily-specificity of the peptidome in the family Viperidae.

Aisha Munawar1, Maria Trusch, Dessislava Georgieva, Patrick Spencer, Violette Frochaux, Sönke Harder, Raghuvir K Arni, Deyan Duhalov, Nicolay Genov, Hartmut Schlüter, Christian Betzel.   

Abstract

Snake venom peptidomes are valuable sources of pharmacologically active compounds. We analyzed the peptidic fractions (peptides with molecular masses < 10,000 Da) of venoms of Vipera ammodytes meridionalis (Viperinae), the most toxic snake in Europe, and Bothrops jararacussu (Crotalinae), an extremely poisonous snake of South America. Liquid chromatography/mass spectrometry (LC/MS), direct infusion electrospray mass spectrometry (ESI-MS) and matrix-assisted desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) were applied to characterize the peptides of both snake venoms. 32 bradykinin-potentiating peptides (BPPs) were identified in the Crotalinae venom and their sequences determined. 3 metalloproteinase inhibitors, 10 BPPs and a Kunitz-type inhibitor were observed in the Viperinae venom peptidome. Variability in the C-terminus of homologous BPPs was observed, which can influence the pharmacological effects. The data obtained so far show a subfamily specificity of the venom peptidome in the Viperidae family: BPPs are the major peptide component of the Crotalinae venom peptidome lacking Kunitz-type inhibitors (with one exception) while the Viperinae venom, in addition to BPPs, can contain peptides of the bovine pancreatic trypsin inhibitor family. We found indications for a post-translational phosphorylation of serine residues in Bothrops jararacussu venom BPP (S[combining low line]QGLPPGPPIP), which could be a regulatory mechanism in their interactions with ACE, and might influence the hypotensive effect. Homology between venom BPPs from Viperidae snakes and venom natriuretic peptide precursors from Elapidae snakes suggests a structural similarity between the respective peptides from the peptidomes of both snake families. The results demonstrate that the venoms of both snakes are rich sources of peptides influencing important physiological systems such as blood pressure regulation and hemostasis. The data can be used for pharmacological and medical applications.

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Year:  2011        PMID: 21959992     DOI: 10.1039/c1mb05309d

Source DB:  PubMed          Journal:  Mol Biosyst        ISSN: 1742-2051


  11 in total

1.  Peptidomics of three Bothrops snake venoms: insights into the molecular diversification of proteomes and peptidomes.

Authors:  Alexandre K Tashima; André Zelanis; Eduardo S Kitano; Danielle Ianzer; Robson L Melo; Vanessa Rioli; Sávio S Sant'anna; Ana C G Schenberg; Antônio C M Camargo; Solange M T Serrano
Journal:  Mol Cell Proteomics       Date:  2012-08-06       Impact factor: 5.911

2.  In cellulo phosphorylation induces pharmacological reprogramming of maurocalcin, a cell-penetrating venom peptide.

Authors:  Michel Ronjat; Wei Feng; Lucie Dardevet; Yao Dong; Sawsan Al Khoury; Franck C Chatelain; Virginie Vialla; Samir Chahboun; Florian Lesage; Hervé Darbon; Isaac N Pessah; Michel De Waard
Journal:  Proc Natl Acad Sci U S A       Date:  2016-04-11       Impact factor: 11.205

Review 3.  Protease inhibitors from marine venomous animals and their counterparts in terrestrial venomous animals.

Authors:  Caroline B F Mourão; Elisabeth F Schwartz
Journal:  Mar Drugs       Date:  2013-06-14       Impact factor: 5.118

4.  Proteomic Analyses of Agkistrodon contortrix contortrix Venom Using 2D Electrophoresis and MS Techniques.

Authors:  Aleksandra Bocian; Małgorzata Urbanik; Konrad Hus; Andrzej Łyskowski; Vladimír Petrilla; Zuzana Andrejčáková; Monika Petrillová; Jaroslav Legáth
Journal:  Toxins (Basel)       Date:  2016-12-13       Impact factor: 4.546

Review 5.  Snake Venom Peptides: Tools of Biodiscovery.

Authors:  Aisha Munawar; Syed Abid Ali; Ahmed Akrem; Christian Betzel
Journal:  Toxins (Basel)       Date:  2018-11-14       Impact factor: 4.546

6.  Proteome and Peptidome of Vipera berus berus Venom.

Authors:  Aleksandra Bocian; Małgorzata Urbanik; Konrad Hus; Andrzej Łyskowski; Vladimír Petrilla; Zuzana Andrejčáková; Monika Petrillová; Jaroslav Legath
Journal:  Molecules       Date:  2016-10-19       Impact factor: 4.411

7.  Elapid snake venom analyses show the specificity of the peptide composition at the level of genera Naja and Notechis.

Authors:  Aisha Munawar; Maria Trusch; Dessislava Georgieva; Diana Hildebrand; Marcel Kwiatkowski; Henning Behnken; Sönke Harder; Raghuvir Arni; Patrick Spencer; Hartmut Schlüter; Christian Betzel
Journal:  Toxins (Basel)       Date:  2014-02-28       Impact factor: 4.546

8.  Quantitative Proteomic Analysis of Venoms from Russian Vipers of Pelias Group: Phospholipases A₂ are the Main Venom Components.

Authors:  Sergey I Kovalchuk; Rustam H Ziganshin; Vladislav G Starkov; Victor I Tsetlin; Yuri N Utkin
Journal:  Toxins (Basel)       Date:  2016-04-12       Impact factor: 4.546

9.  Isolation and characterization of Bradykinin potentiating peptides from Agkistrodon bilineatus venom.

Authors:  Aisha Munawar; Anum Zahid; Amr Negm; Ahmed Akrem; Patrick Spencer; Christian Betzel
Journal:  Proteome Sci       Date:  2016-01-14       Impact factor: 2.480

10.  Isolation and biochemical characterization of bradykinin-potentiating peptides from Bitis gabonica rhinoceros.

Authors:  Tamara M Fucase; Juliana M Sciani; Ingrid Cavalcante; Vincent L Viala; Bruno B Chagas; Daniel C Pimenta; Patrick J Spencer
Journal:  J Venom Anim Toxins Incl Trop Dis       Date:  2017-06-26
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