Sánchez-Moguel Ignacio, Montiel Carmina, Bustos-Jaimes Ismael
Departamento de Bioquímica, Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), Mexico City 04510, Mexico.
Departamento de Alimentos y Biotecnología, Facultad de Química, Universidad Nacional Autónoma de México (UNAM), Mexico City 04510, Mexico.
Pathogens. 2023 Aug 2;12(8):1007. doi: 10.3390/pathogens12081007.
Virus-like particles (VLPs) comprise one or many structural components of virions, except their genetic material. Thus, VLPs keep their structural properties of cellular recognition while being non-infectious. VLPs of Parvovirus B19 (B19V) can be produced by the heterologous expression of their structural proteins VP1 and VP2 in bacteria. These proteins are purified under denaturing conditions, refolded, and assembled into VLPs. Moreover, chimeric forms of VP2 have been constructed to harbor peptides or functional proteins on the surface of the particles without dropping their competence to form VLPs, serving as presenting nanoparticles. The in-vitro assembly approach offers exciting possibilities for the composition of VLPs, as more than one chimeric form of VP2 can be included in the assembly stage, producing multifunctional VLPs. Here, the heterologous expression and in-vitro assembly of B19V structural proteins and their chimeras are reviewed. Considerations for the engineering of the structural proteins of B19V are also discussed. Finally, the construction of multifunctional VLPs and their future potential as innovative medical tools are examined.
病毒样颗粒(VLPs)由病毒粒子的一种或多种结构成分组成,但不包括其遗传物质。因此,VLPs在无感染性的同时保留了其细胞识别的结构特性。细小病毒B19(B19V)的VLPs可通过在细菌中异源表达其结构蛋白VP1和VP2来产生。这些蛋白质在变性条件下纯化、复性并组装成VLPs。此外,已经构建了VP2的嵌合形式,使其在颗粒表面携带肽或功能蛋白,而不会丧失其形成VLPs的能力,可作为呈递纳米颗粒。体外组装方法为VLPs的组成提供了令人兴奋的可能性,因为在组装阶段可以包含不止一种VP2嵌合形式,从而产生多功能VLPs。在此,对B19V结构蛋白及其嵌合体的异源表达和体外组装进行综述。还讨论了B19V结构蛋白工程的相关考虑因素。最后,研究了多功能VLPs的构建及其作为创新医疗工具的未来潜力。