Sequential bottom-up assembly of mechanically stabilized synthetic cells by microfluidics

被引:0
|
作者
Marian Weiss
Johannes Patrick Frohnmayer
Lucia Theresa Benk
Barbara Haller
Jan-Willi Janiesch
Thomas Heitkamp
Michael Börsch
Rafael B. Lira
Rumiana Dimova
Reinhard Lipowsky
Eberhard Bodenschatz
Jean-Christophe Baret
Tanja Vidakovic-Koch
Kai Sundmacher
Ilia Platzman
Joachim P. Spatz
机构
[1] Max Planck Institute for Medical Research,Department of Cellular Biophysics
[2] University of Heidelberg,Department of Biophysical Chemistry
[3] Single-Molecule Microscopy Group,undefined
[4] Jena University Hospital,undefined
[5] Friedrich Schiller University Jena,undefined
[6] Theory & Bio-Systems,undefined
[7] Max Planck Institute of Colloids and Interfaces,undefined
[8] Laboratory for Fluid Dynamics,undefined
[9] Pattern Formation and Biocomplexity,undefined
[10] Max Planck Institute for Dynamics and Self-Organization,undefined
[11] Droplets,undefined
[12] Membranes and Interfaces,undefined
[13] Max Planck Institute for Dynamics and Self-Organization,undefined
[14] Soft Micro Systems,undefined
[15] CNRS,undefined
[16] Univ. Bordeaux,undefined
[17] CRPP,undefined
[18] Process System Engineering,undefined
[19] Max Planck Institute for Dynamics of Complex Technical Systems,undefined
[20] Otto-von-Guericke University Magdeburg,undefined
[21] Process Systems Engineering,undefined
[22] Universitätsplatz 2,undefined
关键词
D O I
10.1038/nmat5005
中图分类号
学科分类号
摘要
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.
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页码:89 / 96
页数:7
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