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      Spontaneous Reorganization of DNA-Based Polymers in Higher Ordered Structures Fueled by RNA

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          Abstract

          We demonstrate a strategy that allows for the spontaneous reconfiguration of self-assembled DNA polymers exploiting RNA as chemical fuel. To do this, we have rationally designed orthogonally addressable DNA building blocks that can be transiently deactivated by RNA fuels and subtracted temporarily from participation in the self-assembly process. Through a fine modulation of the rate at which the building blocks are reactivated we can carefully control the final composition of the polymer and convert a disordered polymer in a higher order polymer, which is disfavored from a thermodynamic point of view. We measure the dynamic reconfiguration via fluorescent signals and confocal microscopy, and we derive a kinetic model that captures the experimental results. Our approach suggests a novel route toward the development of biomolecular materials in which engineered chemical reactions support the autonomous spatial reorganization of multiple components.

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          A guided tour into subcellular colocalization analysis in light microscopy.

          It is generally accepted that the functional compartmentalization of eukaryotic cells is reflected by the differential occurrence of proteins in their compartments. The location and physiological function of a protein are closely related; local information of a protein is thus crucial to understanding its role in biological processes. The visualization of proteins residing on intracellular structures by fluorescence microscopy has become a routine approach in cell biology and is increasingly used to assess their colocalization with well-characterized markers. However, image-analysis methods for colocalization studies are a field of contention and enigma. We have therefore undertaken to review the most currently used colocalization analysis methods, introducing the basic optical concepts important for image acquisition and subsequent analysis. We provide a summary of practical tips for image acquisition and treatment that should precede proper colocalization analysis. Furthermore, we discuss the application and feasibility of colocalization tools for various biological colocalization situations and discuss their respective strengths and weaknesses. We have created a novel toolbox for subcellular colocalization analysis under ImageJ, named JACoP, that integrates current global statistic methods and a novel object-based approach.
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            Functional supramolecular polymers.

            Supramolecular polymers can be random and entangled coils with the mechanical properties of plastics and elastomers, but with great capacity for processability, recycling, and self-healing due to their reversible monomer-to-polymer transitions. At the other extreme, supramolecular polymers can be formed by self-assembly among designed subunits to yield shape-persistent and highly ordered filaments. The use of strong and directional interactions among molecular subunits can achieve not only rich dynamic behavior but also high degrees of internal order that are not known in ordinary polymers. They can resemble, for example, the ordered and dynamic one-dimensional supramolecular assemblies of the cell cytoskeleton and possess useful biological and electronic functions.
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              Three-dimensional structures self-assembled from DNA bricks.

              We describe a simple and robust method to construct complex three-dimensional (3D) structures by using short synthetic DNA strands that we call "DNA bricks." In one-step annealing reactions, bricks with hundreds of distinct sequences self-assemble into prescribed 3D shapes. Each 32-nucleotide brick is a modular component; it binds to four local neighbors and can be removed or added independently. Each 8-base pair interaction between bricks defines a voxel with dimensions of 2.5 by 2.5 by 2.7 nanometers, and a master brick collection defines a "molecular canvas" with dimensions of 10 by 10 by 10 voxels. By selecting subsets of bricks from this canvas, we constructed a panel of 102 distinct shapes exhibiting sophisticated surface features, as well as intricate interior cavities and tunnels.
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                Author and article information

                Journal
                J Am Chem Soc
                J Am Chem Soc
                ja
                jacsat
                Journal of the American Chemical Society
                American Chemical Society
                0002-7863
                1520-5126
                29 November 2021
                08 December 2021
                : 143
                : 48
                : 20296-20301
                Affiliations
                []Department of Chemistry, University of Rome Tor Vergata , Via della Ricerca Scientifica, 00133 Rome, Italy
                []Department of Bioengineering, University of California at Los Angeles , 410 Westwood Plaza, Los Angeles, California 90095, United States
                [§ ]Department of Mechanical and Aerospace Engineering and of Bioengineering, University of California at Los Angeles , 420 Westwood Plaza, Los Angeles, California 90095, United States
                []Department of Chemical Sciences, University of Padua , Via Marzolo 1, 35131 Padua, Italy
                Author notes
                Author information
                https://orcid.org/0000-0003-1103-2668
                https://orcid.org/0000-0001-6664-822X
                https://orcid.org/0000-0003-4941-8646
                Article
                10.1021/jacs.1c09503
                8662731
                34843256
                688e7c2d-6fff-481e-bfb8-cab41c7e90e6
                © 2021 American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 08 September 2021
                Funding
                Funded by: H2020 European Research Council, doi 10.13039/100010663;
                Award ID: 819160
                Funded by: Ministero dell''Istruzione, dell''Università e della Ricerca, doi NA;
                Award ID: 2017E44A9P
                Funded by: Associazione Italiana per la Ricerca sul Cancro, doi 10.13039/501100005010;
                Award ID: 21965
                Funded by: H2020 Marie SkÃ…?odowska-Curie Actions, doi 10.13039/100010665;
                Award ID: 896962
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                ja1c09503
                ja1c09503

                Chemistry
                Chemistry

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