Martins Sofia A, Santos Joana, Cabo Verde Sandra, Correia João D G, Melo Rita
Centro de Ciências e Tecnologias Nucleares, Instituto Superior Técnico, Universidade de Lisboa, Estrada Nacional 10, ao km 139,7, 2695-066 Loures, Portugal.
Departamento de Engenharia e Ciências Nucleares, Instituto Superior Técnico, Universidade de Lisboa, Estrada Nacional 10, ao km 139,7, 2695-066 Loures, Portugal.
Bioengineering (Basel). 2022 Nov 19;9(11):713. doi: 10.3390/bioengineering9110713.
Virus-like particles (VLPs) are nanoplatforms comprised of one or more viral proteins with the capacity to self-assemble without viral genetic material. VLPs arise as promising nanoparticles (NPs) that can be exploited as vaccines, as drug delivery vehicles or as carriers of imaging agents. Engineered antibody constructs, namely single-chain variable fragments (scFv), have been explored as relevant molecules to direct NPs to their target. A vector containing the scFv of an antibody, aimed at the human epidermal growth factor receptor 2 (HER2) and fused to the human immunodeficiency virus (HIV) protein gp41, was previously constructed. The work herein describes the early results concerning the production and the characterization of HIV-1-based VLPs expressing this protein, which could function as potential non-toxic tools for transporting drugs and/or imaging agents.
病毒样颗粒(VLPs)是由一种或多种病毒蛋白组成的纳米平台,能够在没有病毒遗传物质的情况下进行自我组装。VLPs作为一种有前景的纳米颗粒(NPs)出现,可以用作疫苗、药物递送载体或成像剂载体。工程化抗体构建体,即单链可变片段(scFv),已被探索作为将NPs导向其靶标的相关分子。先前构建了一种载体,该载体包含针对人表皮生长因子受体2(HER2)的抗体的scFv,并与人免疫缺陷病毒(HIV)蛋白gp41融合。本文的工作描述了关于表达该蛋白的基于HIV-1的VLPs的生产和表征的早期结果,这些VLPs可作为运输药物和/或成像剂的潜在无毒工具。