Abstract

A new era has begun in which pathogens have become useful scaffolds for nanotechnology applications. In this research/study, an attempt has been made to generate an empty cargo-like architecture from a plant pathogenic virus named Squash leaf curl China virus (SLCCNV). In this approach, SLCCNV coat protein monomers are obtained efficiently by using a yeast Pichia pastoris expression system. Further, dialysis of purified SLCCNV-CP monomers against various pH modified (5-10) disassembly and assembly buffers produced a self-assembled "Nanocargo"-like architecture, which also exhibited an ability to encapsulate magnetic nanoparticles in vitro. Bioinformatics tools were also utilized to predict the possible self-assembly kinetics and bioconjugation sites of coat protein monomers. Significantly, an in vitro biocompatibility study using SLCCNV-Nanocargo particles showed low toxicity to the cells, which eventually proved as a potential nanobiomaterial for biomedical applications.

Highlights

  • There has always been a high demand for biological entities which have the ability to act as a multifaceted scaffold or template

  • We chose a well-known plant pathogenic virus of the Begomovirus isolates of Squash leaf curl China virus (SLCCNV) for this study, whose molecular pathogenicity we had already established in our laboratory studies

  • The expression of the entire Begomovirus unmodified coat protein subunits was first achieved in the eukaryotic yeast Pichia pastoris system

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Summary

Introduction

There has always been a high demand for biological entities which have the ability to act as a multifaceted scaffold or template. They can be produced in sufficient quantities with recombinant technologies Their properties are programmable through changes at the genome level to produce novel functionalities[14].The VLPs that are currently being developed for biomedical applications share the common property of being self-assembling – they form a closed capsid-like structure with an altered symmetryfrom a limited number of protein subunits, which are referred to by various terms with the prefix of "nano"-cage, -carrier, -cargo, and -container[8]. The true reason for our choice of this virus is no study yet to done to reveal the structural and assembly properties of Begomoviruses, which are crucial for coat-host protein interaction mediated pathogenicity studies

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