masterThesis
Avaliação funcional e estrutural de um novo peptídeo antimicrobiano do escorpião Tityus stigmurus
Fecha
2014-03-31Registro en:
MELO, Edinara Targino de. Avaliação funcional e estrutural de um novo peptídeo antimicrobiano do escorpião Tityus stigmurus. 2014. 100f. Dissertação (Mestrado em Ciências Farmacêuticas) - Centro de Ciências da Saúde, Universidade Federal do Rio Grande do Norte, Natal, 2014.
Autor
Melo, Edinara Targino de
Resumen
In Brazil, there is a high incidence of venomous animals. Among them,
scorpions are highlighted by their medical importance, and for being their venom a
source of several molecules with biological and pharmacological activity not yet fully
understood, including several bioactive peptides. Antimicrobial peptides (AMPs) are
components of the immune system in prokaryotes and eukaryotes, used in the first line
of defense against microorganisms. In the present study, we characterized the first PAM
previously identified through transcriptome of the venom gland of the scorpion Tityus
stigmurus, named Stigmurin. The characteristics of Stigmurin were investigated by
computational modeling and construction of dendrogram. In vitro tests investigated the
antibacterial, antifungal, haemolytic and cytotoxic effects of crude venom and
Stigmurin. In addition, the structural characteristics of Stigmurin were investigated by
circular dochroism in water, 2, 2 , 2- trifluoethanol (TFE) and sodium dodecyl sulfate
(SDS) and the models were refined by molecular dynamics simulations. The results
showed that the selected sequence encodes a mature protein of 17 amino acid residues
and the dendrogram reveals a case of convergent evolution. The crude venom showed
no antimicrobial activity, however, Stigmurin exhibited a broad spectrum of
antibacterial activity, with minimal inhibitory concentrations (MIC) ranging from 31.25
and 250 µg/mL for different strains, while the hemolytic activity at these concentrations
was low. In cytotoxicity studies, the crude venom was unable to reduce cell viability in
VERO E6 cells; in contrast, its activity in SiHa cells was significantly higher,
corresponding to IC50 of 3.6 µg/mL. For Stigmurin the concentration sable to decrease
cell viability of Vero E6 and SiHa cells in 50% were 275.67 µg/mL and 212.54 µg/mL,
respectively. The dichroism spectra revealed the conformational flexibility, with
predominating extended and β–sheet structures, as well as a remark able renaturation
ability. The results suggest that Stigmurin could be considered as a potential antiinfective
drug