Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities

• Autor(a) principal: Boldrini-França, Johara
• Data de Publicação: 2020
• Outros Autores: Pinheiro-Junior, Ernesto Lopes, Peigneur, Steve, Pucca, Manuela Berto, Cerni, Felipe Augusto, Borges, Rafael Junqueira [UNESP], Costa, Tássia Rafaella, Carone, Sante Emmanuel Imai, Fontes, Marcos Roberto de Mattos [UNESP], Sampaio, Suely Vilela, Arantes, Eliane Candiani, Tytgat, Jan
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UNESP
• Texto Completo: http://dx.doi.org/10.1038/s41598-020-61258-x; http://hdl.handle.net/11449/201617

Snake venom serine proteases (SVSPs) are complex and multifunctional enzymes, acting primarily on hemostasis. In this work, we report the hitherto unknown inhibitory effect of a SVSP, named collinein-1, isolated from the venom of Crotalus durissus collilineatus, on a cancer-relevant voltage-gated potassium channel (hEAG1). Among 12 voltage-gated ion channels tested, collinein-1 selectively inhibited hEAG1 currents, with a mechanism independent of its enzymatic activity. Corroboratively, we demonstrated that collinein-1 reduced the viability of human breast cancer cell line MCF7 (high expression of hEAG1), but does not affect the liver carcinoma and the non-tumorigenic epithelial breast cell lines (HepG2 and MCF10A, respectively), which present low expression of hEAG1. In order to obtain both functional and structural validation of this unexpected discovery, where an unusually large ligand acts as an inhibitor of an ion channel, a recombinant and catalytically inactive mutant of collinein-1 (His43Arg) was produced and found to preserve its capability to inhibit hEAG1. A molecular docking model was proposed in which Arg79 of the SVSP 99-loop interacts directly with the potassium selectivity filter of the hEAG1 channel.