7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Functional DNA-based cytoskeletons for synthetic cells

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The cytoskeleton is an essential component of a cell. It controls the cell shape, establishes the internal organization, and performs vital biological functions. Building synthetic cytoskeletons that mimic key features of their natural counterparts delineates a crucial step towards synthetic cells assembled from the bottom up. To this end, DNA nanotechnology represents one of the most promising routes, given the inherent sequence specificity, addressability and programmability of DNA. Here we demonstrate functional DNA-based cytoskeletons operating in microfluidic cell-sized compartments. The synthetic cytoskeletons consist of DNA tiles self-assembled into filament networks. These filaments can be rationally designed and controlled to imitate features of natural cytoskeletons, including reversible assembly and ATP-triggered polymerization, and we also explore their potential for guided vesicle transport in cell-sized confinement. Also, they possess engineerable characteristics, including assembly and disassembly powered by DNA hybridization or aptamer–target interactions and autonomous transport of gold nanoparticles. This work underpins DNA nanotechnology as a key player in building synthetic cells.

          Abstract

          Cytoskeletons are essential components of cells that perform a variety of tasks, and artificial cytoskeletons that perform these functions are required for the bottom-up assembly of synthetic cells. Now, a multi-functional cytoskeleton mimic has been engineered from DNA, consisting of confined DNA filaments that are capable of reversible self-assembly and transport of gold nanoparticles and vesicular cargo.

          Related collections

          Most cited references44

          • Record: found
          • Abstract: found
          • Article: not found

          Folding DNA to create nanoscale shapes and patterns.

          'Bottom-up fabrication', which exploits the intrinsic properties of atoms and molecules to direct their self-organization, is widely used to make relatively simple nanostructures. A key goal for this approach is to create nanostructures of high complexity, matching that routinely achieved by 'top-down' methods. The self-assembly of DNA molecules provides an attractive route towards this goal. Here I describe a simple method for folding long, single-stranded DNA molecules into arbitrary two-dimensional shapes. The design for a desired shape is made by raster-filling the shape with a 7-kilobase single-stranded scaffold and by choosing over 200 short oligonucleotide 'staple strands' to hold the scaffold in place. Once synthesized and mixed, the staple and scaffold strands self-assemble in a single step. The resulting DNA structures are roughly 100 nm in diameter and approximate desired shapes such as squares, disks and five-pointed stars with a spatial resolution of 6 nm. Because each oligonucleotide can serve as a 6-nm pixel, the structures can be programmed to bear complex patterns such as words and images on their surfaces. Finally, individual DNA structures can be programmed to form larger assemblies, including extended periodic lattices and a hexamer of triangles (which constitutes a 30-megadalton molecular complex).
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            A DNA-fuelled molecular machine made of DNA.

            Molecular recognition between complementary strands of DNA allows construction on a nanometre length scale. For example, DNA tags may be used to organize the assembly of colloidal particles, and DNA templates can direct the growth of semiconductor nanocrystals and metal wires. As a structural material in its own right, DNA can be used to make ordered static arrays of tiles, linked rings and polyhedra. The construction of active devices is also possible--for example, a nanomechanical switch, whose conformation is changed by inducing a transition in the chirality of the DNA double helix. Melting of chemically modified DNA has been induced by optical absorption, and conformational changes caused by the binding of oligonucleotides or other small groups have been shown to change the enzymatic activity of ribozymes. Here we report the construction of a DNA machine in which the DNA is used not only as a structural material, but also as 'fuel'. The machine, made from three strands of DNA, has the form of a pair of tweezers. It may be closed and opened by addition of auxiliary strands of 'fuel' DNA; each cycle produces a duplex DNA waste product.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Forcing cells into shape: the mechanics of actomyosin contractility.

              Actomyosin-mediated contractility is a highly conserved mechanism for generating mechanical stress in animal cells and underlies muscle contraction, cell migration, cell division and tissue morphogenesis. Whereas actomyosin-mediated contractility in striated muscle is well understood, the regulation of such contractility in non-muscle and smooth muscle cells is less certain. Our increased understanding of the mechanics of actomyosin arrays that lack sarcomeric organization has revealed novel modes of regulation and force transmission. This work also provides an example of how diverse mechanical behaviours at cellular scales can arise from common molecular components, underscoring the need for experiments and theories to bridge the molecular to cellular length scales.
                Bookmark

                Author and article information

                Contributors
                kevin.jahnke@mr.mpg.de
                na.liu@pi2.uni-stuttgart.de
                kerstin.goepfrich@mr.mpg.de
                Journal
                Nat Chem
                Nat Chem
                Nature Chemistry
                Nature Publishing Group UK (London )
                1755-4330
                1755-4349
                20 June 2022
                20 June 2022
                2022
                : 14
                : 8
                : 958-963
                Affiliations
                [1 ]GRID grid.5719.a, ISNI 0000 0004 1936 9713, 2nd Physics Institute, University of Stuttgart, ; Stuttgart, Germany
                [2 ]GRID grid.419552.e, ISNI 0000 0001 1015 6736, Max Planck Institute for Solid State Research, ; Stuttgart, Germany
                [3 ]GRID grid.414703.5, ISNI 0000 0001 2202 0959, Biophysical Engineering Group, Max Planck Institute for Medical Research, ; Heidelberg, Germany
                [4 ]GRID grid.7700.0, ISNI 0000 0001 2190 4373, Department of Physics and Astronomy, , Heidelberg University, ; Heidelberg, Germany
                Author information
                http://orcid.org/0000-0001-7311-6993
                http://orcid.org/0000-0001-5831-3382
                http://orcid.org/0000-0003-2115-3551
                Article
                945
                10.1038/s41557-022-00945-w
                9359917
                35725773
                9c8989cd-6f48-4f2a-8915-f970c3e34c82
                © The Author(s) 2022

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 5 March 2021
                : 4 April 2022
                Funding
                Funded by: FundRef https://doi.org/10.13039/100010663, EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council);
                Award ID: ERC Dynamic Nano
                Award ID: ERC Dynamic Nano
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100007569, Carl-Zeiss-Stiftung (Carl Zeiss Foundation);
                Funded by: FundRef https://doi.org/10.13039/501100004189, Max-Planck-Gesellschaft (Max Planck Society);
                Funded by: FundRef https://doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft (German Research Foundation);
                Award ID: EXC-2082/1 - 390761711
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s), under exclusive licence to Springer Nature Limited 2022

                Chemistry
                biopolymers,dna and rna,synthetic biology,dna nanostructures,permeation and transport
                Chemistry
                biopolymers, dna and rna, synthetic biology, dna nanostructures, permeation and transport

                Comments

                Comment on this article