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      Designer DNA architecture offers precise and multivalent spatial pattern-recognition for viral sensing and inhibition

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          Abstract

          DNA, when folded into nanostructures with a specific shape, is capable of spacing and arranging binding sites into a complex geometric pattern with nanometre precision. Here we demonstrate a designer DNA nanostructure that can act as a template to display multiple binding motifs with precise spatial pattern-recognition properties, and that this approach can confer exceptional sensing and potent viral inhibitory capabilities. A star-shaped DNA architecture, carrying five molecular beacon-like motifs, was constructed to display ten dengue envelope protein domain III (ED3)-targeting aptamers into a two-dimensional pattern precisely matching the spatial arrangement of ED3 clusters on the dengue (DENV) viral surface. The resulting multivalent interactions provide high DENV-binding avidity. We show that this structure is a potent viral inhibitor and that it can act as a sensor by including a fluorescent output to report binding. Our molecular-platform design strategy could be adapted to detect and combat other disease-causing pathogens by generating the requisite ligand patterns on customized DNA nanoarchitectures.

          Abstract

          DNA is capable of self-assembling into a wide range of user-defined structures and so can be used as a scaffold to arrange binding motifs with nanometre precision. Now, DNA has been used to accurately display aptamers that fit the repeated epitope pattern of a dengue viral antigen to produce a nanostructure that can be a potent viral inhibitor or a fluorescent sensor.

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          Most cited references43

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          Molecular beacons: probes that fluoresce upon hybridization.

          We have developed novel nucleic acid probes that recognize and report the presence of specific nucleic acids in homogeneous solutions. These probes undergo a spontaneous fluorogenic conformational change when they hybridize to their targets. Only perfectly complementary targets elicit this response, as hybridization does not occur when the target contains a mismatched nucleotide or a deletion. The probes are particularly suited for monitoring the synthesis of specific nucleic acids in real time. When used in nucleic acid amplification assays, gene detection is homogeneous and sensitive, and can be carried out in a sealed tube. When introduced into living cells, these probes should enable the origin, movement, and fate of specific mRNAs to be traced.
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            Nucleic acid junctions and lattices.

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              Molecularly Self-Assembled Nucleic Acid Nanoparticles for Targeted In Vivo siRNA Delivery

              Nanoparticles are employed for delivering therapeutics into cells 1,2 . However, size, shape, surface chemistry and the presentation of targeting ligands on the surface of nanoparticles can affect circulation half-life and biodistribution, cell specific internalization, excretion, toxicity, and efficacy 3-7 . A variety of materials have been explored for delivering small interfering RNAs (siRNAs) - a therapeutic agent that suppresses the expression of targeted genes 8,9 . However, conventional delivery nanoparticles such as liposomes and polymeric systems are heterogeneous in size, composition and surface chemistry, and this can lead to suboptimal performance, lack of tissue specificity and potential toxicity 10-12 . Here, we show that self-assembled DNA tetrahedral nanoparticles with a well-defined size can deliver siRNAs into cells and silence target genes in tumours. Monodisperse nanoparticles are prepared through the self-assembly of complementary DNA strands. Because the DNA strands are easily programmable, the size of the nanoparticles and the spatial orientation and density of cancer targeting ligands (such as peptides and folate) on the nanoparticle surface can be precisely controlled. We show that at least three folate molecules per nanoparticle is required for optimal delivery of the siRNAs into cells and, gene silencing occurs only when the ligands are in the appropriate spatial orientation. In vivo, these nanoparticles showed a longer blood circulation time (t1/2 ∼ 24.2 min) than the parent siRNA (t1/2 ∼ 6 min).
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                Author and article information

                Contributors
                iamjchao@njupt.edu.cn
                xingw@illinois.edu
                Journal
                Nat Chem
                Nat Chem
                Nature Chemistry
                Nature Publishing Group UK (London )
                1755-4330
                1755-4349
                25 November 2019
                2020
                : 12
                : 1
                : 26-35
                Affiliations
                [1 ]ISNI 0000 0004 0369 3615, GRID grid.453246.2, Key Laboratory for Organic Electronics and Information Displays and Jiangsu, Key Laboratory for Biosensors, , Institute of Advanced Materials, National Synergetic Innovation Center for Advanced Materials, Nanjing University of Posts and Telecommunications, ; Nanjing, China
                [2 ]ISNI 0000 0001 2160 9198, GRID grid.33647.35, Department of Chemistry and Chemical Biology, Center for Biotechnology and Interdisciplinary Studies, , Rensselaer Polytechnic Institute, ; Troy, NY USA
                [3 ]ISNI 0000 0001 2171 9311, GRID grid.21107.35, Department of Neuroscience, , Johns Hopkins University, ; Baltimore, MD USA
                [4 ]ISNI 0000 0001 2160 9198, GRID grid.33647.35, Department of Chemical and Biological Engineering, Center for Biotechnology and Interdisciplinary Studies, , Rensselaer Polytechnic Institute, ; Troy, NY USA
                [5 ]ISNI 0000 0004 0435 9002, GRID grid.465543.5, Wadsworth Center, New York State Department of Health, ; Albany, NY USA
                [6 ]ISNI 0000 0004 1936 8753, GRID grid.137628.9, Department of Chemistry, , New York University, ; New York, NY USA
                [7 ]ISNI 0000 0004 1936 8753, GRID grid.137628.9, Center for Soft Matter Research, , New York University, ; New York, NY USA
                [8 ]ISNI 0000 0004 1936 9991, GRID grid.35403.31, Department of Chemistry, Micro and Nanotechnology Laboratory (MNTL), Carl R. Woese Institute for Genomic Biology (IGB), , University of Illinois at Urbana-Champaign, ; Urbana, IL USA
                Author information
                http://orcid.org/0000-0003-3549-8606
                http://orcid.org/0000-0003-2803-3704
                http://orcid.org/0000-0003-1030-9944
                http://orcid.org/0000-0001-9930-3287
                Article
                369
                10.1038/s41557-019-0369-8
                6925649
                31767992
                0653534c-7192-4210-8ec0-240ac6055a5f
                © The Author(s), under exclusive licence to Springer Nature Limited 2019

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 25 March 2019
                : 8 October 2019
                Categories
                Article
                Custom metadata
                © The Author(s), under exclusive licence to Springer Nature Limited 2020

                Chemistry
                dna nanostructures,biosensors,nanomedicine,nucleic-acid therapeutics
                Chemistry
                dna nanostructures, biosensors, nanomedicine, nucleic-acid therapeutics

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