<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shetty RM</submitter><funding>Division of Computing and Communication Foundations</funding><funding>Arizona Biomedical Research Commission</funding><funding>NIH Office of the Director</funding><funding>NIAID NIH HHS</funding><funding>Office of Naval Research Global</funding><funding>Division of Civil, Mechanical and Manufacturing Innovation</funding><pagination>11441-11450</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9701110</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(7)</volume><pubmed_abstract>Large-scale nanoarrays of single biomolecules enable high-throughput assays while unmasking the underlying heterogeneity within ensemble populations. Until recently, creating such grids which combine the advantages of microarrays and single-molecule experiments (SMEs) has been particularly challenging due to the mismatch between the size of these molecules and the resolution of top-down fabrication techniques. DNA origami placement (DOP) combines two powerful techniques to address this issue: (i) DNA origami, which provides a ∼100 nm self-assembled template for single-molecule organization with 5 nm resolution and (ii) top-down lithography, which patterns these DNA nanostructures, transforming them into functional nanodevices via large-scale integration with arbitrary substrates. Presently, this technique relies on state-of-the-art infrastructure and highly trained personnel, making it prohibitively expensive for researchers. Here, we introduce a cleanroom-free, $1 benchtop technique to create meso-to-macro-scale DNA origami nanoarrays using self-assembled colloidal nanoparticles, thereby circumventing the need for top-down fabrication. We report a maximum yield of 74%, 2-fold higher than the statistical limit of 37% imposed on non-specific molecular loading alternatives. Furthermore, we provide a proof-of-principle for the ability of this nanoarray platform to transform traditionally low-throughput, stochastic, single-molecule assays into high-throughput, deterministic ones, without compromising data quality. Our approach has the potential to democratize single-molecule nanoarrays and demonstrates their utility as a tool for biophysical assays and diagnostics.</pubmed_abstract><journal>ACS nano</journal><pubmed_title>Bench-Top Fabrication of Single-Molecule Nanoarrays by DNA Origami Placement.</pubmed_title><pmcid>PMC9701110</pmcid><funding_grant_id>CCF-1317694</funding_grant_id><funding_grant_id>CMMI-1636364</funding_grant_id><funding_grant_id>N00014-17-1-2610</funding_grant_id><funding_grant_id>DP2 AI144247</funding_grant_id><funding_grant_id>1DP2AI144247</funding_grant_id><funding_grant_id>ADHS17-00007401</funding_grant_id><funding_grant_id>N00014-18-1-2649</funding_grant_id><pubmed_authors>Rothemund PWK</pubmed_authors><pubmed_authors>Gopinath A</pubmed_authors><pubmed_authors>Shetty RM</pubmed_authors><pubmed_authors>Brady SR</pubmed_authors><pubmed_authors>Hariadi RF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bench-Top Fabrication of Single-Molecule Nanoarrays by DNA Origami Placement.</name><description>Large-scale nanoarrays of single biomolecules enable high-throughput assays while unmasking the underlying heterogeneity within ensemble populations. Until recently, creating such grids which combine the advantages of microarrays and single-molecule experiments (SMEs) has been particularly challenging due to the mismatch between the size of these molecules and the resolution of top-down fabrication techniques. DNA origami placement (DOP) combines two powerful techniques to address this issue: (i) DNA origami, which provides a ∼100 nm self-assembled template for single-molecule organization with 5 nm resolution and (ii) top-down lithography, which patterns these DNA nanostructures, transforming them into functional nanodevices via large-scale integration with arbitrary substrates. Presently, this technique relies on state-of-the-art infrastructure and highly trained personnel, making it prohibitively expensive for researchers. Here, we introduce a cleanroom-free, $1 benchtop technique to create meso-to-macro-scale DNA origami nanoarrays using self-assembled colloidal nanoparticles, thereby circumventing the need for top-down fabrication. We report a maximum yield of 74%, 2-fold higher than the statistical limit of 37% imposed on non-specific molecular loading alternatives. Furthermore, we provide a proof-of-principle for the ability of this nanoarray platform to transform traditionally low-throughput, stochastic, single-molecule assays into high-throughput, deterministic ones, without compromising data quality. Our approach has the potential to democratize single-molecule nanoarrays and demonstrates their utility as a tool for biophysical assays and diagnostics.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jul</publication><modification>2025-04-25T20:57:04.914Z</modification><creation>2025-04-06T08:33:14.086Z</creation></dates><accession>S-EPMC9701110</accession><cross_references><pubmed>34228915</pubmed><doi>10.1021/acsnano.1c01150</doi></cross_references></HashMap>