Sainsbury Frank, Saxena Pooja, Aljabali Alaa A A, Saunders Keith, Evans David J, Lomonossoff George P
Australian Institute for Bioengineering and Nanotechnology, University of Queensland, St-Lucia, QLD, Australia.
Methods Mol Biol. 2014;1108:139-53. doi: 10.1007/978-1-62703-751-8_11.
The development of methods for the production of empty Cowpea mosaic virus (CPMV) virus-like particles (VLPs) that are devoid of RNA, eVLPs, has renewed promise in CPMV capsid technologies. The recombinant nature of CPMV eVLP production means that the extent and variety of genetic modifications that may be incorporated into the particles is theoretically much greater than those that can be made to infectious CPMV virions due to restrictions on viral propagation of the latter. Free of the infectious agent, the genomic RNA, these particles are now finding potential uses in vaccine development, in vivo imaging, drug delivery, and other nanotechnology applications that make use of internal loading of the empty particles. Here we describe methods for the genetic modification and production of CPMV eVLPs and describe techniques useful for their characterization.
生产不含RNA的空豇豆花叶病毒(CPMV)病毒样颗粒(eVLP)的方法的发展,为CPMV衣壳技术带来了新的希望。CPMV eVLP生产的重组性质意味着,由于后者病毒传播的限制,理论上可以纳入颗粒的基因修饰的程度和种类比可对感染性CPMV病毒粒子进行的修饰要大得多。这些颗粒不含感染性因子基因组RNA,目前正在疫苗开发、体内成像、药物递送以及利用空颗粒内部装载的其他纳米技术应用中找到潜在用途。在这里,我们描述了CPMV eVLP的基因修饰和生产方法,并描述了对其进行表征有用的技术。