Reengineering viruses and virus-like particles through chemical functionalization strategies.

Mark Thomas Smith, Anna K Hawes, Bradley Charles Bundy

Journal: Current opinion in biotechnology 2013;24(4):620-6

PMID: 23465756

Abstract

Increasing demands from nanotechnology require increasingly more rigorous methods to control nanoparticle traits such as assembly, size, morphology, monodispersity, stability, and reactivity. Viruses are a compelling starting point for engineering nanoparticles, as eons of natural biological evolution have instilled diverse and desirable traits. The next step is to reengineer these viruses into something functional and useful. These reengineered particles, or virus-based nanoparticles (VNPs), are the foundation for many promising new technologies in drug delivery, targeted delivery, vaccines, imaging, and biocatalysis. To achieve these end goals, VNPs must often be manipulated genetically and post-translationally. We review prevailing strategies of genetic and noncovalent functionalization and focus on the covalent modifications using natural and unnatural amino acid residues.

Copyright © 2013 Elsevier Ltd. All rights reserved.

Address: Department of Chemical Engineering, Brigham Young University, United States.
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