Weiss Marian, Frohnmayer Johannes Patrick, Benk Lucia Theresa, Haller Barbara, Janiesch Jan-Willi, Heitkamp Thomas, Börsch Michael, Lira Rafael B, Dimova Rumiana, Lipowsky Reinhard, Bodenschatz Eberhard, Baret Jean-Christophe, Vidakovic-Koch Tanja, Sundmacher Kai, Platzman Ilia, Spatz Joachim P
Department of Cellular Biophysics, Max Planck Institute for Medical Research, Jahnstraße 29, 69120 Heidelberg, Germany.
Department of Biophysical Chemistry, University of Heidelberg, Im Neuenheimer Feld 253, 69120 Heidelberg, Germany.
Nat Mater. 2018 Jan;17(1):89-96. doi: 10.1038/nmat5005. Epub 2017 Oct 16.
Compartments for the spatially and temporally controlled assembly of biological processes are essential towards cellular life. Synthetic mimics of cellular compartments based on lipid-based protocells lack the mechanical and chemical stability to allow their manipulation into a complex and fully functional synthetic cell. Here, we present a high-throughput microfluidic method to generate stable, defined sized liposomes termed 'droplet-stabilized giant unilamellar vesicles (dsGUVs)'. The enhanced stability of dsGUVs enables the sequential loading of these compartments with biomolecules, namely purified transmembrane and cytoskeleton proteins by microfluidic pico-injection technology. This constitutes an experimental demonstration of a successful bottom-up assembly of a compartment with contents that would not self-assemble to full functionality when simply mixed together. Following assembly, the stabilizing oil phase and droplet shells are removed to release functional self-supporting protocells to an aqueous phase, enabling them to interact with physiologically relevant matrices.
用于生物过程在空间和时间上可控组装的区室对于细胞生命至关重要。基于脂质原细胞的细胞区室的合成模拟物缺乏机械和化学稳定性,无法将其操纵成复杂且功能齐全的合成细胞。在此,我们提出一种高通量微流控方法,以生成稳定的、尺寸确定的脂质体,称为“液滴稳定的巨型单层囊泡(dsGUVs)”。dsGUVs增强的稳定性使得能够通过微流控皮升注射技术将这些区室依次装载生物分子,即纯化的跨膜蛋白和细胞骨架蛋白。这构成了一个成功的自下而上组装区室的实验证明,该区室的内容物在简单混合时不会自组装成完整功能。组装后,去除稳定油相和液滴壳,将功能性自支撑原细胞释放到水相中,使其能够与生理相关基质相互作用。