DNA Nanostructures on Membranes as Tools for Synthetic Biology

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DNA Nanostructures on Membranes as Tools for Synthetic Biology Aleksander Czogalla, Henri G. Franquelim, Petra Schwille  Biophysical Journal  Volume 110, Issue 8, Pages 1698-1707 (April 2016) DOI: 10.1016/j.bpj.2016.03.015 Copyright © 2016 The Authors Terms and Conditions

Figure 1 Lipophilic nucleic acids and their assembly on liposomes. (A) Cholesteryl-TEG-nucleotide. (B) Schematic representation of vesicle fusion induced by cholesteryl-TEG-oligonucleotide zippers in analogy to SNARE Fusion complex (reproduced with permission from (43), copyright 2008 American Chemical Society). (C) Hydrodynamic radii (RH) of liposomes during step-by-step assembly of DNA pseudohexagons on their surface (squares: asymmetric protocol, circles: symmetric protocol) (reproduced with permission from (21), copyright The Royal Society of Chemistry). To see this figure in color, go online. Biophysical Journal 2016 110, 1698-1707DOI: (10.1016/j.bpj.2016.03.015) Copyright © 2016 The Authors Terms and Conditions

Figure 2 Switchable partitioning of lipophilic DNA structures on Ld/Lo membrane domains. (A) Oligo DNA/PNA complex colocalized as four-component complexes in the Ld domain, but after cleavage of the complex with restriction endonuclease (EcoR1-HF) the resulting amphipathic components separated from each other. Ratios between the fluorescence intensities in the Lo and Ld phases are given (reproduced with permission from (40), copyright 2012 American Chemical Society). (B) Origami DNA nanorods partition into the Ld phase (marked with DiD), but after addition of Mg2+ ions they translocate into the Lo phase, which is fully reversible after removal of the magnesium (with EDTA). Scale bars correspond to 10 μm. Biophysical Journal 2016 110, 1698-1707DOI: (10.1016/j.bpj.2016.03.015) Copyright © 2016 The Authors Terms and Conditions

Figure 3 Controllable assembly of lipophilic origami DNA nanostructures on lipid membranes. (A) Origami DNA hexagons with photoresponsive modifications were reversibly assembled or disassembled upon irradiation with light of a different wavelength (reproduced with permission from (73), copyright 2015 American Chemical Society). (B) Origami DNA blocks were polymerized into one-dimensional or two-dimensional complexes via specific DNA oligonucleotides depicted in blue or orange, respectively (reproduced with permission from (60), copyright 2015 American Chemical Society). (C) Two populations of amphipathic origami DNA monoliths (labeled either with Alexa488 (green) or Alexa647 (red)) form regular array, as shown on a transmission electron microscopy (TEM) image (scale bar is 100 nm), which at high surface densities deform a GUV (scale bar is 10 μm) (reproduced with permission from (61), copyright 2015 John Wiley and Sons). Biophysical Journal 2016 110, 1698-1707DOI: (10.1016/j.bpj.2016.03.015) Copyright © 2016 The Authors Terms and Conditions

Figure 4 A variety of membrane-anchored origami DNA nanostructures. (A) Cholesteryl-anchored (orange) origami DNA channel consisting of a barrel-like cap (white) and a transmembrane stem (red), which spontaneously dock to liposomes, as shown on a TEM image (B) (reproduced with permission from (64), copyright 2012 The American Association for the Advancement of Science). (C) Virus-inspired membrane-enveloped DNA nanostructures for biomedical applications; color-enhanced TEM image (D) represents the DNA nanostructure (dark blue) tightly wrapped with unilamellar membrane (light blue) (reproduced with permission from (70) copyright 2014 American Chemical Society). Scale bars 50 nm. Biophysical Journal 2016 110, 1698-1707DOI: (10.1016/j.bpj.2016.03.015) Copyright © 2016 The Authors Terms and Conditions