Burger Michael, Brigger Finn, Mantella Valeria, Leroux Jean-Christophe
Swiss Federal Institute of Technology Zurich (ETHZ), Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, Vladimir-Prelog-Weg 3, 8093 Zurich, Switzerland.
Swiss Federal Institute of Technology Zurich (ETHZ), Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, Vladimir-Prelog-Weg 3, 8093 Zurich, Switzerland.
Cell Rep Methods. 2025 Jun 16;5(6):101073. doi: 10.1016/j.crmeth.2025.101073. Epub 2025 Jun 9.
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.
本文报道了一种有效的方法,可在不使用有机溶剂的情况下,于生理缓冲液中、在低蛋白质/DNA浓度下,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。使用人类线粒体转录因子A(TFAM)实现DNA压缩,TFAM与质粒DNA(pDNA)混合时会形成复合物(TFAMoplexes)。在人类膜联蛋白A4的帮助下,这些复合物被募集到预先形成的巨型单层囊泡(GUVs)表面,从而在膜上富集。随后,使用短时间超声脉冲将TFAMoplex包被的GUVs转化为小囊泡。该方法可将约40%的TFAMoplexes封装到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,这种方法能够创建复杂的分子组装体,为广泛的生化和生物医学应用铺平道路。