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mRNA 的离子脂质纳米颗粒合成与包封。

mRNA Synthesis and Encapsulation in Ionizable Lipid Nanoparticles.

机构信息

Malaghan Institute of Medical Research, Wellington, New Zealand.

Hugh Green Cytometry Centre, Malaghan Institute of Medical Research, Wellington, New Zealand.

出版信息

Curr Protoc. 2023 Sep;3(9):e898. doi: 10.1002/cpz1.898.

Abstract

mRNA vaccines have recently generated significant interest due to their success during the COVID-19 pandemic. Their success is due to advances in mRNA design and encapsulation into ionizable lipid nanoparticles (iLNPs). This has highlighted the potential for the use of mRNA-iLNPs in other settings such as cancer, gene therapy, or vaccines for different infectious diseases. Here, we describe the production of mRNA-iLNPs using commercially available reagents that are suitable for use as vaccines and therapeutics. This article contains detailed protocols for the synthesis of mRNA by in vitro transcription with enzymatic capping and tailing and the encapsulation of the mRNA into iLNPs using the ionizable lipid DLin-MC3-DMA. DLin-MC3-DMA is often used as a benchmark for new formulations and provides an efficient delivery vehicle for screening mRNA design. The protocol also describes how the formulation can be adapted to other lipids. Finally, a stepwise methodology is presented for the characterization and quality control of mRNA-iLNPs, including measuring mRNA concentration and encapsulation efficiency, particle size, and zeta potential. © 2023 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Synthesis of mRNA by in vitro transcription and enzymatic capping and tailing Basic Protocol 2: Encapsulation of mRNA into ionizable lipid nanoparticles Alternate Protocol: Small-scale encapsulation of mRNA using preformed vesicles Basic Protocol 3: Characterization and quality control of mRNA ionizable lipid nanoparticles.

摘要

mRNA 疫苗在 COVID-19 大流行期间取得了巨大成功,因此最近引起了广泛关注。其成功归因于 mRNA 设计和封装到可离子化脂质纳米颗粒(iLNPs)方面的进展。这突出了在其他环境中使用 mRNA-iLNPs 的潜力,例如癌症、基因治疗或针对不同传染病的疫苗。在这里,我们描述了使用商业上可获得的试剂生产 mRNA-iLNPs 的方法,这些试剂适合用作疫苗和治疗剂。本文包含了通过酶促加帽和加尾的体外转录合成 mRNA 以及使用可离子化脂质 DLin-MC3-DMA 将 mRNA 封装到 iLNPs 中的详细方案。DLin-MC3-DMA 通常用作新配方的基准,并为筛选 mRNA 设计提供了有效的递送载体。该方案还描述了如何将配方改编为其他脂质。最后,提出了一种逐步的方法来对 mRNA-iLNPs 进行表征和质量控制,包括测量 mRNA 浓度和封装效率、粒径和 zeta 电位。© 2023 作者。Wiley 期刊出版公司出版的《当代协议》。基本方案 1:体外转录和酶促加帽和加尾合成 mRNA 基本方案 2:将 mRNA 封装到可离子化脂质纳米颗粒中 可选方案:使用预形成的囊泡进行小规模封装 mRNA 基本方案 3:mRNA 可离子化脂质纳米颗粒的表征和质量控制。

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