CPP-Ts: a new intracellular calcium channel modulator and a promising tool for drug delivery in cancer cells

CPP-Ts:一种新的细胞内钙通道调节剂和一种有前途的癌细胞药物输送工具

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作者:Bárbara Bruna Ribeiro de Oliveira-Mendes, Carolina Campolina Rebello Horta, Anderson Oliveira do Carmo, Gabriela Lago Biscoto, Douglas Ferreira Sales-Medina, Hortênsia Gomes Leal, Pedro Ferreira Pinto Brandão-Dias, Sued Eustáquio Mendes Miranda, Carla Jeane Aguiar, Valbert Nascimento Cardoso, André

Abstract

Scorpion sting envenoming impacts millions of people worldwide, with cardiac effects being one of the main causes of death on victims. Here we describe the first Ca2+ channel toxin present in Tityus serrulatus (Ts) venom, a cell penetrating peptide (CPP) named CPP-Ts. We show that CPP-Ts increases intracellular Ca2+ release through the activation of nuclear InsP3R of cardiomyocytes, thereby causing an increase in the contraction frequency of these cells. Besides proposing a novel subfamily of Ca2+ active toxins, we investigated its potential use as a drug delivery system targeting cancer cell nucleus using CPP-Ts's nuclear-targeting property. To this end, we prepared a synthetic CPP-Ts sub peptide14-39 lacking pharmacological activity which was directed to the nucleus of specific cancer cell lines. This research identifies a novel subfamily of Ca2+ active toxins and provides new insights into biotechnological applications of animal venoms.

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