| Literature DB >> 28754346 |
Kamila Soares Lopes1, Gabriel Avohay Alves Campos1, Luana Cristina Camargo1, Adolfo Carlos Barros de Souza1, Beatriz Vasconcelos Ibituruna1, Ana Carolina Martins Magalhães1, Lucas Ferreira da Rocha1, Alessa Bembom Garcia1, Mosar Correa Rodrigues1, Dagon Manoel Ribeiro1, Michelle Cruz Costa1, Manuel Humberto Mera López1, Luciana Marangni Nolli1, Fernando Zamudio-Zuniga2, Lourival Domingos Possani2, Elisabeth Ferroni Schwartz1, Márcia Renata Mortari3.
Abstract
Chatergellus communis is a wasp species endemic to the neotropical region and its venom constituents have never been described. In this study, two peptides from C. communis venom, denominated Communis and Communis-AAAA, were chemically and biologically characterized. In respect to the chemical characterization, the following amino acid sequences and molecular masses were identified: Communis: Ile-Asn-Trp-Lys-Ala-Ile-Leu-Gly-Lys-Ile-Gly-Lys-COOH (1340.9Da) Communis-AAAA: Ile-Asn-Trp-Lys-Ala-Ile-Leu-Gly-Lys-Ile-Gly-Lys-Ala-Ala-Ala-Ala-Val-Xle-NH2 (1836.3Da). Furthermore, their biological effects were compared, accounting for the differences in structural characteristics between the two peptides. To this end, three biological assays were performed in order to evaluate the hyperalgesic, edematogenic and hemolytic effects of these molecules. Communis-AAAA, unlike Communis, showed a potent hemolytic activity with EC50=142.6μM. Moreover, the highest dose of Communis-AAAA (2nmol/animal) induced hyperalgesia in mice. On the other hand, Communis (10nmol/animal) was able to induce edema but did not present hemolytic or hyperalgesic activity. Although both peptides have similarities in linear structures, we demonstrated the distinct biological effects of Communis and Communis-AAAA. This is the first study with Chartegellus communis venom, and both Communis and Communis-AAAA are unpublished peptides.Entities:
Keywords: Algesia; Edema; Hemolysis; Multiple alanine residues; Peptide; Wasp venom
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Year: 2017 PMID: 28754346 DOI: 10.1016/j.peptides.2017.07.012
Source DB: PubMed Journal: Peptides ISSN: 0196-9781 Impact factor: 3.750