通过膜联蛋白介导的膜募集和超声将蛋白质/DNA复合物封装到单层脂质体中。

IF 4.3 Q1 BIOCHEMICAL RESEARCH METHODS
Cell Reports Methods Pub Date : 2025-06-16 Epub Date: 2025-06-09 DOI:10.1016/j.crmeth.2025.101073
Michael Burger, Finn Brigger, Valeria Mantella, Jean-Christophe Leroux
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引用次数: 0

摘要

本文报道了一种有效的方案,将天然蛋白质/DNA复合物封装到由天然脂质组成的单层囊泡中,而不使用有机溶剂,在生理缓冲液中,在低蛋白质/DNA浓度下。DNA压缩是通过人线粒体转录因子A (TFAM)实现的,当与质粒DNA (pDNA)混合时,TFAM形成复合物(TFAMoplexes)。这些复合物在人膜联蛋白A4的帮助下被招募到预制的巨型单层囊泡(GUVs)的表面,从而集中在膜上。随后,使用短超声脉冲将tfamoplex涂层的guv转化为小泡。该方法可将约40%的TFAMoplexes包封在平均流体动力学直径为121 nm的单层脂质体中。通过利用人类蛋白质的功能,这种方法可以创建复杂的分子组装,为广泛的生化和生物医学应用铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Encapsulation of protein/DNA complexes into unilamellar liposomes via annexin-mediated membrane recruitment and sonication.

This paper reports an effective protocol to encapsulate native protein/DNA complexes into unilamellar vesicles composed of natural lipids without the use of organic solvents, in physiological buffers, and at low protein/DNA concentrations. DNA compaction is achieved with the human mitochondrial transcription factor A (TFAM), which forms complexes (TFAMoplexes) when mixed with plasmid DNA (pDNA). The complexes are recruited to the surface of preformed giant unilamellar vesicles (GUVs) with the help of human annexin A4 and thereby concentrated at the membranes. This is followed by transforming the TFAMoplex-coated GUVs into small vesicles using short sonication pulses. This method results in the encapsulation of around 40% of the TFAMoplexes into unilamellar liposomes with an average hydrodynamic diameter of 121 nm. By harnessing the functions of human proteins, this approach enables the creation of complex molecular assemblies that will pave the way for a wide array of biochemical and biomedical applications.

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来源期刊
Cell Reports Methods
Cell Reports Methods Chemistry (General), Biochemistry, Genetics and Molecular Biology (General), Immunology and Microbiology (General)
CiteScore
3.80
自引率
0.00%
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0
审稿时长
111 days
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