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脂质纳米粒递送系统中 mRNA 活性丧失的新机制。

A novel mechanism for the loss of mRNA activity in lipid nanoparticle delivery systems.

机构信息

Moderna, Inc., 200 Technology Square, Cambridge, MA, USA.

出版信息

Nat Commun. 2021 Nov 22;12(1):6777. doi: 10.1038/s41467-021-26926-0.

Abstract

Lipid nanoparticle (LNP)-formulated mRNA vaccines were rapidly developed and deployed in response to the SARS-CoV-2 pandemic. Due to the labile nature of mRNA, identifying impurities that could affect product stability and efficacy is crucial to the long-term use of nucleic-acid based medicines. Herein, reversed-phase ion pair high performance liquid chromatography (RP-IP HPLC) was used to identify a class of impurity formed through lipid:mRNA reactions; such reactions are typically undetectable by traditional mRNA purity analytical techniques. The identified modifications render the mRNA untranslatable, leading to loss of protein expression. Specifically, electrophilic impurities derived from the ionizable cationic lipid component are shown to be responsible. Mechanisms implicated in the formation of reactive species include oxidation and subsequent hydrolysis of the tertiary amine. It thus remains critical to ensure robust analytical methods and stringent manufacturing control to ensure mRNA stability and high activity in LNP delivery systems.

摘要

脂质纳米颗粒 (LNP) 配方的 mRNA 疫苗是为应对 SARS-CoV-2 大流行而迅速开发和部署的。由于 mRNA 的不稳定性,鉴定可能影响产品稳定性和疗效的杂质对于长期使用基于核酸的药物至关重要。在此,反相离子对高效液相色谱 (RP-IP HPLC) 用于鉴定一类通过脂质:mRNA 反应形成的杂质;此类反应通常无法通过传统的 mRNA 纯度分析技术检测到。鉴定出的修饰使 mRNA 无法翻译,导致蛋白表达丧失。具体来说,源自可离子化阳离子脂质成分的亲电杂质被证明是负责的。形成反应性物质的机制包括叔胺的氧化和随后的水解。因此,仍然必须确保具有强大的分析方法和严格的制造控制,以确保 LNP 递送系统中的 mRNA 稳定性和高活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/291c/8608879/e996aca92baa/41467_2021_26926_Fig1_HTML.jpg

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