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自我扩增mRNA与自我扩增DNA的比较功能分析

Comparative Function Analysis of Self-Amplifying mRNA and Self-Amplifying DNA.

作者信息

Li Wenting, Wang Yiming, Wang Chen, Huo Yi-Xin, Lu Yuan

机构信息

Key Laboratory of Molecular Medicine and Biotherapy, Aerospace Center Hospital, School of Life Science, Beijing Institute of Technology, Beijing, 100081, China.

State Key Laboratory of Green Biomanufacturing, Key Laboratory of Industrial Biocatalysis (Ministry of Education), Department of Chemical Engineering, Tsinghua University, Beijing, 100084, China.

出版信息

Chembiochem. 2025 Jul 11;26(13):e202500110. doi: 10.1002/cbic.202500110. Epub 2025 Jun 17.

Abstract

A promising approach to address the transient translation mRNA drugs is the development of self-amplifying mRNA (SAM). Similarly, SAM's DNA template, self-amplifying DNA (SAD), can also play a role in self-amplifying the target mRNA. However, there is still a lack of sufficient valid information on the comparative analysis of SAM and SAD. Therefore, various vectors and delivery systems are selected to compare and analyze the transfection efficiency of SAM and SAD, and transfection conditions for SAM are optimized. It is found that SAD and SAM have obviously different preferences in transfection conditions, and there is also a gap in their transfection efficiencies under the same conditions. Furthermore, the optimal transfection dose of SAD and SAM and the optimal incubation time after transfection are also determined. This study provides valuable information on SAM transfection and its difference with SAD, and offers an option of selecting appropriate nucleic acid vectors for drug development.

摘要

一种解决瞬时翻译mRNA药物问题的有前景的方法是开发自扩增mRNA(SAM)。同样,SAM的DNA模板,即自扩增DNA(SAD),也可以在自扩增靶mRNA中发挥作用。然而,关于SAM和SAD的比较分析仍缺乏足够的有效信息。因此,选择各种载体和递送系统来比较和分析SAM和SAD的转染效率,并优化SAM的转染条件。发现SAD和SAM在转染条件上有明显不同的偏好,并且在相同条件下它们的转染效率也存在差距。此外,还确定了SAD和SAM的最佳转染剂量以及转染后的最佳孵育时间。本研究提供了关于SAM转染及其与SAD差异的有价值信息,并为药物开发选择合适的核酸载体提供了一种选择。

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