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      Programmable CRISPR-responsive smart materials

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          Abstract

          Stimuli-responsive materials activated by biological signals play an increasingly important role in biotechnology applications. We exploit the programmability of CRISPR-associated nucleases to actuate hydrogels containing DNA as a structural element or as an anchor for pendant groups. After activation by guide RNA–defined inputs, Cas12a cleaves DNA in the gels, thereby converting biological information into changes in material properties. We report four applications: (i) branched poly(ethylene glycol) hydrogels releasing DNA-anchored compounds, (ii) degradable polyacrylamide-DNA hydrogels encapsulating nanoparticles and live cells, (iii) conductive carbon-black–DNA hydrogels acting as degradable electrical fuses, and (iv) a polyacrylamide-DNA hydrogel operating as a fluidic valve with an electrical readout for remote signaling. These materials allow for a range of in vitro applications in tissue engineering, bioelectronics, and diagnostics.

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          Most cited references41

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          A study of the nucleation and growth processes in the synthesis of colloidal gold

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            Designing hydrogels for controlled drug delivery

            Hydrogel delivery systems can leverage therapeutically beneficial outcomes of drug delivery and have found clinical use. Hydrogels can provide spatial and temporal control over the release of various therapeutic agents, including small-molecule drugs, macromolecular drugs and cells. Owing to their tunable physical properties, controllable degradability and capability to protect labile drugs from degradation, hydrogels serve as a platform in which various physiochemical interactions with the encapsulated drugs control their release. In this Review, we cover multiscale mechanisms underlying the design of hydrogel drug delivery systems, focusing on physical and chemical properties of the hydrogel network and the hydrogel-drug interactions across the network, mesh, and molecular (or atomistic) scales. We discuss how different mechanisms interact and can be integrated to exert fine control in time and space over the drug presentation. We also collect experimental release data from the literature, review clinical translation to date of these systems, and present quantitative comparisons between different systems to provide guidelines for the rational design of hydrogel delivery systems.
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              Three-dimensional self-assembly of graphene oxide and DNA into multifunctional hydrogels.

              Graphene and its functionalized derivatives are unique and versatile building blocks for self-assembly to fabricate graphene-based functional materials with hierarchical microstructures. Here we report a strategy for three-dimensional self-assembly of graphene oxide sheets and DNA to form multifunctional hydrogels. The hydrogels possess high mechanical strength, environmental stability, and dye-loading capacity, and a exhibit self-healing property. This study provides a new insight for the assembly of functionalized graphene with other building blocks, especially biomolecules, which will help rational design and preparation of hierarchical graphene-based materials.
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                Author and article information

                Journal
                Science
                Science
                American Association for the Advancement of Science (AAAS)
                0036-8075
                1095-9203
                August 22 2019
                August 23 2019
                August 22 2019
                August 23 2019
                : 365
                : 6455
                : 780-785
                Article
                10.1126/science.aaw5122
                31439791
                e104a4a4-1b30-4bee-93be-c49b1668f0d9
                © 2019

                http://www.sciencemag.org/about/science-licenses-journal-article-reuse

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