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利用生物工厂植物生产用纳米抗体修饰的马铃薯Y病毒衍生纳米颗粒。

Production of Potyvirus-Derived Nanoparticles Decorated with a Nanobody in Biofactory Plants.

作者信息

Martí Maricarmen, Merwaiss Fernando, Butković Anamarija, Daròs José-Antonio

机构信息

Instituto de Biología Molecular y Celular de Plantas (Consejo Superior de Investigaciones Científicas-Universitat Politècnica de València), Valencia, Spain.

出版信息

Front Bioeng Biotechnol. 2022 Mar 31;10:877363. doi: 10.3389/fbioe.2022.877363. eCollection 2022.

Abstract

Viral nanoparticles (VNPs) have recently attracted attention for their use as building blocks for novel materials to support a range of functions of potential interest in nanotechnology and medicine. Viral capsids are ideal for presenting small epitopes by inserting them at an appropriate site on the selected coat protein (CP). VNPs presenting antibodies on their surfaces are considered highly promising tools for therapeutic and diagnostic purposes. Due to their size, nanobodies are an interesting alternative to classic antibodies for surface presentation. Nanobodies are the variable domains of heavy-chain (VHH) antibodies from animals belonging to the family Camelidae, which have several properties that make them attractive therapeutic molecules, such as their small size, simple structure, and high affinity and specificity. In this work, we have produced genetically encoded VNPs derived from two different potyviruses-the largest group of RNA viruses that infect plants-decorated with nanobodies. We have created a VNP derived from zucchini yellow mosaic virus (ZYMV) decorated with a nanobody against the green fluorescent protein (GFP) in zucchini () plants. As reported for other viruses, the expression of ZYMV-derived VNPs decorated with this nanobody was only made possible by including a picornavirus 2A splicing peptide between the fused proteins, which resulted in a mixed population of unmodified and decorated CPs. We have also produced tobacco etch virus (TEV)-derived VNPs in plants decorated with the same nanobody against GFP. Strikingly, in this case, VNPs could be assembled by direct fusion of the nanobody to the viral CP with no 2A splicing involved, likely resulting in fully decorated VNPs. For both expression systems, correct assembly and purification of the recombinant VNPs was confirmed by transmission electron microscope; the functionality of the CP-fused nanobody was assessed by western blot and binding assays. In sum, here we report the production of genetically encoded plant-derived VNPs decorated with a nanobody. This system may be an attractive alternative for the sustainable production in plants of nanobody-containing nanomaterials for diagnostic and therapeutic purposes.

摘要

病毒纳米颗粒(VNPs)最近因其作为新型材料的构建单元而受到关注,这些新型材料可支持纳米技术和医学中一系列潜在的重要功能。病毒衣壳非常适合通过将小表位插入所选衣壳蛋白(CP)上的合适位点来呈现。表面呈现抗体的VNPs被认为是用于治疗和诊断目的的极有前景的工具。由于其大小,纳米抗体是用于表面呈现的经典抗体的有趣替代品。纳米抗体是来自骆驼科动物的重链可变区(VHH)抗体,它们具有多种使其成为有吸引力的治疗分子的特性,例如它们的小尺寸、简单结构以及高亲和力和特异性。在这项工作中,我们生产了源自两种不同马铃薯Y病毒(最大的感染植物的RNA病毒组)的基因编码VNPs,并装饰有纳米抗体。我们创建了一种源自西葫芦黄花叶病毒(ZYMV)的VNP,在西葫芦()植物中用针对绿色荧光蛋白(GFP)的纳米抗体进行了装饰。正如其他病毒所报道的那样,只有通过在融合蛋白之间包含微小RNA病毒2A剪接肽,才使得用这种纳米抗体装饰的ZYMV衍生的VNPs得以表达,这导致了未修饰和修饰的CP的混合群体。我们还在植物中生产了烟草蚀纹病毒(TEV)衍生的VNPs,并用相同的针对GFP的纳米抗体进行了装饰。引人注目的是,在这种情况下,VNPs可以通过纳米抗体与病毒CP的直接融合进行组装,而无需2A剪接,这可能导致完全装饰的VNPs。对于这两种表达系统,通过透射电子显微镜确认了重组VNPs的正确组装和纯化;通过蛋白质印迹和结合试验评估了与CP融合的纳米抗体的功能。总之,我们在此报告了用纳米抗体装饰的基因编码植物源VNPs的生产。该系统可能是用于诊断和治疗目的的含纳米抗体的纳米材料在植物中可持续生产的有吸引力的替代方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57a2/9008781/cdbe0b3170d5/fbioe-10-877363-g001.jpg

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