A pH-Responsive Virus-Like Particle as a Protein Cage for a Targeted Delivery

A stimuli-responsive protein self-assembly offers promising utility as a protein nanocage for biotechnological and medical applications. Herein, the development of a virus-like particle (VLP) that undergoes a transition between assembly and disassembly under a neutral and acidic pH, respectively, for a targeted delivery is reported. The structure of the bacteriophage P22 coat protein is used for the computational design of coat subunits that self-assemble into a pH-responsive VLP. Subunit designs are generated through iterative computational cycles of histidine substitutions and evaluation of the interaction energies among the subunits under an acidic and neutral pH. The top subunit designs are tested and one that is assembled into a VLP showing the highest pH-dependent structural transition is selected. The cryo-EM structure of the VLP is determined, and the structural basis of a pH-triggered disassembly is delineated. The utility of the designed VLP is exemplified through the targeted delivery of a cytotoxic protein cargo into tumor cells in a pH-dependent manner. These results provide strategies for the development of self-assembling protein architectures with new functionality for diverse applications. A virus-like particle (VLP) showing pH-responsive assembly and disassembly is developed for targeted drug delivery through the computational design of bacteriophage P22 coat proteins. The underlying mechanism for the pH responsiveness of the designed VLP is demonstrated by determining its cryo-EM structure. The utility of the VLP is exemplified by the pH-dependent delivery of a tumor-targeting cytotoxic protein.image

Automated summary

This study develops a virus-like particle (VLP) that shows pH-responsive assembly and disassembly for targeted drug delivery through the computational design of bacteriophage P22 coat proteins. The cryo-EM structure of the designed VLP is determined, demonstrating the underlying mechanism of pH responsiveness. The utility of the VLP is exemplified by delivering a tumor-targeting cytotoxic protein in a pH-dependent manner.