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封装在丝中的RNA的稳定化

Stabilization of RNA Encapsulated in Silk.

作者信息

He Jiuyang, Yavuz Burcin, Kluge Jonathan A, Li Adrian B, Omenetto Fiorenzo G, Kaplan David L

机构信息

Department of Biomedical Engineering, Tufts University, 4 Colby Street, Medford, Massachusetts 02155, United States.

Vaxess Technologies, c/o Pagliuca Harvard Life Lab, 127 Western Avenue, Allston, Massachusetts 02134, United States.

出版信息

ACS Biomater Sci Eng. 2018 May 14;4(5):1708-1715. doi: 10.1021/acsbiomaterials.8b00207. Epub 2018 Mar 26.

Abstract

The use of mRNA and miRNA as diagnostic parameters and therapeutic agents has drawn wide interest both clinically and in research. However, RNA is a labile molecule, which requires strict storage conditions, often including cold temperatures or dry environments, in order to preserve RNA integrity. Achieving this requires huge costs for storage and added difficulty in transport. To address these issues, we introduce a system to encapsulate and store it long-term in dried silk fibroin matrices. At temperatures up to 45 °C, mRNA samples stored in lyophilized silk matrices showed good stability over 1 week, as measured by real-time PCR to assess transcript recovery. While the presence of the silk interfered with the generation of cDNA required for quantitation at roughly 1% w/v (400:1 silk:RNA mass), this phenomenon was resolved by the use of commercial RNA purification kits for silk concentrations up to 4% w/v. A higher concentration of silk correlated with increased thermal protection. As an alternative to lyophilization, RNA was simply air-dried in the presence of aqueous fibroin to create storage matrices. While air-dried matrices composed of low silk content were not protective, higher concentrations were protective and progressively lost additional water over time of storage because of the overall hydrophobic nature of the system. Taken together, these findings provide a new and potentially simpler method for preserving RNA samples for long-term storage and transportation, acting primarily on a water exclusion mechanism.

摘要

将信使核糖核酸(mRNA)和微小核糖核酸(miRNA)用作诊断参数和治疗剂在临床和研究领域都引起了广泛关注。然而,RNA是一种不稳定的分子,为了保持RNA的完整性,需要严格的储存条件,通常包括低温或干燥环境。实现这一点需要巨大的储存成本,并且运输难度也会增加。为了解决这些问题,我们引入了一种系统,可将其封装并长期保存在干燥的丝素蛋白基质中。通过实时聚合酶链反应(PCR)评估转录本回收率,结果显示,在高达45°C的温度下,储存在冻干丝基质中的mRNA样品在1周内表现出良好的稳定性。虽然当丝的浓度约为1% w/v(丝与RNA的质量比为400:1)时,丝的存在会干扰定量所需的互补脱氧核糖核酸(cDNA)的生成,但使用商业RNA纯化试剂盒可解决丝浓度高达4% w/v时的这一现象。较高浓度的丝与增强的热保护作用相关。作为冻干的替代方法,RNA只需在水性丝素蛋白存在的情况下进行风干,即可制成储存基质。虽然由低丝含量组成的风干基质没有保护作用,但较高浓度的基质具有保护作用,并且由于系统的整体疏水性,在储存过程中会逐渐失去额外的水分。综上所述,这些发现提供了一种新的、可能更简单的方法来保存RNA样品以用于长期储存和运输,其主要作用机制是排除水分。

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