de Melo Edinara Targino, Estrela Andréia Bergamo, Santos Elizabeth Cristina Gomes, Machado Paula Renata Lima, Farias Kleber Juvenal Silva, Torres Taffarel Melo, Carvalho Enéas, Lima João Paulo Matos Santos, Silva-Júnior Arnóbio Antonio, Barbosa Euzébio Guimarães, Fernandes-Pedrosa Matheus de Freitas
Laboratório de Tecnologia e Biotecnologia Farmacêutica, Universidade Federal do Rio Grande do Norte, Natal, RN, Brazil.
Laboratório de Imunologia Clínica, Universidade Federal do Rio Grande do Norte, RN, Brazil.
Peptides. 2015 Jun;68:3-10. doi: 10.1016/j.peptides.2015.03.003. Epub 2015 Mar 22.
A new antimicrobial peptide, herein named Stigmurin, was selected based on a transcriptomic analysis of the Brazilian yellow scorpion Tityus stigmurus venom gland, an underexplored source for toxic peptides with possible biotechnological applications. Stigmurin was investigated in silico, by circular dichroism (CD) spectroscopy, and in vitro. The CD spectra suggested that this peptide interacts with membranes, changing its conformation in the presence of an amphipathic environment, with predominance of random coil and beta-sheet structures. Stigmurin exhibited antibacterial and antifungal activity, with minimal inhibitory concentrations ranging from 8.7 to 69.5μM. It was also showed that Stigmurin is toxic against SiHa and Vero E6 cell lines. The results suggest that Stigmurin can be considered a potential anti-infective drug.
基于对巴西黄蝎(Tityus stigmurus)毒腺的转录组分析,筛选出了一种新的抗菌肽,在此命名为Stigmurin。巴西黄蝎毒腺是一个未被充分探索的有毒肽来源,这些有毒肽可能具有生物技术应用价值。通过圆二色(CD)光谱和体外实验对Stigmurin进行了计算机模拟研究。CD光谱表明,该肽与膜相互作用,在两亲性环境中会改变其构象,主要呈现无规卷曲和β-折叠结构。Stigmurin表现出抗菌和抗真菌活性,最小抑菌浓度范围为8.7至69.5μM。研究还表明,Stigmurin对SiHa和Vero E6细胞系有毒性。结果表明,Stigmurin可被视为一种潜在的抗感染药物。