Machida Kodai, Imataka Hiroaki
Department of Materials Science and Chemistry, Graduate School of Engineering, University of Hyogo, Himeji, 671-2201, Japan,
Biotechnol Lett. 2015 Apr;37(4):753-60. doi: 10.1007/s10529-014-1741-9. Epub 2014 Dec 9.
Viral particles and virus-like particles (VLPs) or capsids are becoming important vehicles and templates in bio-imaging, drug delivery and materials sciences. Viral particles are prepared by infecting the host organism but VLPs are obtained from cells that express a capsid protein. Some VLPs are disassembled and then re-assembled to incorporate a material of interest. Cell-free systems, which are amenable to manipulating the viral assembly process, are also available for producing viral particles. Regardless of the production system employed, the particles are functionalized by genetic and/or chemical engineering. Here, we review various methods for producing and functionalizing viral particles and VLPs, and we discuss the merits of each system.
病毒颗粒、病毒样颗粒(VLPs)或衣壳正成为生物成像、药物递送和材料科学领域重要的载体和模板。病毒颗粒通过感染宿主生物体来制备,而VLPs则从表达衣壳蛋白的细胞中获得。一些VLPs被拆解,然后重新组装以纳入感兴趣的材料。适用于操纵病毒组装过程的无细胞系统也可用于生产病毒颗粒。无论采用何种生产系统,颗粒都通过基因工程和/或化学工程进行功能化。在此,我们综述了生产病毒颗粒和VLPs并使其功能化的各种方法,并讨论了每个系统的优点。