Molecular determinants of virus-like nanoparticle assembly in vitro and in animal cell culture

S. S. Soares, L. Pedro, G. Ferreira
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Abstract

Protein nanoparticles, such as virus-like particles (VLPs), consist only of the virus shell without any viral genetic information packaged inside. Similarly to viruses, the structural proteins that comprise a VLP can spontaneously self-assemble to form the particle or can assemble through several intermediate steps. This work addresses the characterization, manipulation and purification of a chimeric simian-human immunodeficiency VLP constructed by fusion of SIV matrix protein (p17) and HIV-1 p6 accessory protein. This fusion protein assembles as spherical nanoparticles of about 80 nm in diameter that are released to the culture media when expressed in HEK 293T cells. A simple two-step purification process was used to purify these nanoparticles. Also, different approaches - multiple-transfections or chemical coupling - were performed to target manipulation. Finally, a new approach for the production of these virus-like particles is described where the structural protein subunits are used and their assembly is promoted in vitro.
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体外和动物细胞培养中病毒样纳米颗粒组装的分子决定因素
蛋白质纳米颗粒,如病毒样颗粒(vlp),仅由病毒外壳组成,内部没有包装任何病毒遗传信息。与病毒类似,构成VLP的结构蛋白可以自发地自组装形成颗粒,也可以通过几个中间步骤进行组装。本研究通过SIV基质蛋白(p17)和HIV-1 p6辅助蛋白的融合构建了嵌合猿人免疫缺陷VLP的表征、操作和纯化。这种融合蛋白组装成直径约80纳米的球形纳米颗粒,在HEK 293T细胞中表达后释放到培养基中。采用简单的两步纯化工艺纯化这些纳米颗粒。此外,不同的方法-多次转染或化学偶联-进行靶操作。最后,描述了一种生产这些病毒样颗粒的新方法,其中使用结构蛋白亚基并在体外促进其组装。
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