Abstract

Melittin (MEL), a small peptide component of bee venom, has been reported to exhibit anti-cancer effects in vitro and in vivo. However, its clinical applicability is disputed because of its non-specific cytotoxicity and haemolytic activity in high treatment doses. Plasma-treated phosphate buffered saline solution (PT-PBS), a solution rich in reactive oxygen and nitrogen species (RONS) can disrupt the cell membrane integrity and induce cancer cell death through oxidative stress-mediated pathways. Thus, PT-PBS could be used in combination with MEL to facilitate its access into cancer cells and to reduce the required therapeutic dose. The aim of our study is to determine the reduction of the effective dose of MEL required to eliminate cancer cells by its combination with PT-PBS. For this purpose, we have optimised the MEL threshold concentration and tested the combined treatment of MEL and PT-PBS on A375 melanoma and MCF7 breast cancer cells, using in vitro, in ovo and in silico approaches. We investigated the cytotoxic effect of MEL and PT-PBS alone and in combination to reveal their synergistic cytological effects. To support the in vitro and in ovo experiments, we showed by computer simulations that plasma-induced oxidation of the phospholipid bilayer leads to a decrease of the free energy barrier for translocation of MEL in comparison with the non-oxidized bilayer, which also suggests a synergistic effect of MEL with plasma induced oxidation. Overall, our findings suggest that MEL in combination with PT-PBS can be a promising combinational therapy to circumvent the non-specific toxicity of MEL, which may help for clinical applicability in the future.

Highlights

  • Melittin (MEL) is a water-soluble cationic amphipathic 26 amino acid α-helical peptide obtained from the honeybee (Apis mellifera) venom [1]

  • We propose the combination of MEL with a solution treated with cold atmospheric plasma (CAP), a novel therapy that could help to overcome the current limitations of MEL

  • After standardisation of the optimal dosages of Plasma-treated phosphate buffered saline solution (PT-PBS), MEL alone and in combination through the MTT and flow cytometry analysis, we investigated the peroxidation of membrane lipids by fluorescence microscopy

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Summary

Introduction

Melittin (MEL) is a water-soluble cationic amphipathic 26 amino acid α-helical peptide obtained from the honeybee (Apis mellifera) venom [1]. It is a very nonspecific cytolytic peptide that rapidly associates with phospholipid cell membranes. It moves in a lateral direction in the membrane, yielding oligomerization, thereby leading to structural defects (e.g., pores) in the cell membrane [2]. Despite the convincing efficacy data against various cancers, its clinical applicability is precluded due to the non-specific toxicity shown at high doses.

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