Reengineering viruses and virus-like particles through chemical functionalization strategies

被引:97
|
作者
Smith, Mark Thomas [1 ]
Hawes, Anna K. [1 ]
Bundy, Bradley Charles [1 ]
机构
[1] Brigham Young Univ, Dept Chem Engn, Provo, UT 84602 USA
基金
美国国家科学基金会; 美国国家航空航天局;
关键词
UNNATURAL AMINO-ACIDS; VIRAL NANOPARTICLES; PROTEINS; PLATFORM; CAPSIDS; DNA; ENCAPSULATION; PEPTIDES; DELIVERY; PLANTS;
D O I
10.1016/j.copbio.2013.01.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:620 / 626
页数:7
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