Genetically engineered nano‐melittin vesicles for multimodal synergetic cancer therapy

Abstract

Melittin, the principal constituent in bee venom, is an attractive candidate for cancer therapy. However, its clinical applications are limited by hemolysis, nonspecific cytotoxicity, and rapid metabolism. Herein, a novel genetically engineered vesicular antibody‐melittin (VAM) drug delivery platform was proposed and validated for targeted cancer combination therapy. VAM generated from the cellular plasma membrane was bio‐synthetically fabricated, with the recombinant protein (hGC33 scFv‐melittin) being harbored and displayed on the cell membrane. The bioactive and targetable nanomelittin conjugated by hGC33 scFv could be released in an MMP14‐responsive manner at tumor sites, which reduced off‐target toxicity, especially the hemolytic activity of melittin. Importantly, VAM could be loaded with small‐molecule drugs or nanoparticles for combination therapy. Nanomelittin formed pores in membranes and disturbed phospholipid bilayers, which allowed the anticancer agents (i.e., chemotherapeutic drug doxorubicin and sonosensitizer purpurin 18 nanoparticles) co‐delivered by VAM to penetrate deeper tumor sites, leading to synergistic therapeutic effects. In particular, the punching effect generated by sonodynamic therapy further improved the immunomodulatory effect of nanomelittin to activate the immune response. Taken together, our findings indicate that clinically translatable VAM‐based strategies represent a universal, promising approach to multimodal synergetic cancer therapy.

Advanced technologies for biomedical applications by emerging researchers in Asia‐Pacific

“…Banstola et al prepared ROS‐responsive thioketal polymer‐based nanoparticles for the simultaneous delivery of small molecules (doxorubicin and R848) and macrophage inflammatory protein‐3 alpha, which were effective in treating breast cancer by inducing immunogenic cell death 15 . Zhang et al genetically fabricated the nano‐melittin vesicles, which can further encapsulate chemotherapeutic drugs or nanoparticles for synergetic cancer therapy 16 . Zhu et al designed various nanobodies of anti‐vascular endothelial growth factor (VEGF) proteins for sustained release of proteins, which provides a novel approach for chronic intravitreal administration of anti‐VEGF proteins 17 .…”

“…15 Zhang et al genetically fabricated the nano-melittin vesicles, which can further encapsulate chemotherapeutic drugs or nanoparticles for synergetic cancer therapy. 16 Zhu et al…”