<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Joaqui-Joaqui MA</submitter><funding>Division of Chemistry</funding><funding>National Institutes of Health</funding><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><funding>National Science Foundation</funding><pagination>2928-2941</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8926058</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(2)</volume><pubmed_abstract>Self-assembly of metallointercalators into DNA nanocages is a rapid and facile approach to synthesize discrete bioinorganic host/guest structures with a high load of metal complexes. Turberfield's DNA tetrahedron can accommodate one intercalator for every two base pairs, which corresponds to 48 metallointercalators per DNA tetrahedron. The affinity of the metallointercalator for the DNA tetrahedron is a function of both the structure of the intercalating ligand and the overall charge of the complex, with a trend in affinity [Ru(bpy)&lt;sub>2&lt;/sub>(dppz)]&lt;sup>2+&lt;/sup> > [Tb-DOTAm-Phen]&lt;sup>3+&lt;/sup> ≫ Tb-DOTA-Phen. Intercalation of the metal complex stabilizes the DNA tetrahedron, resulting in an increase of its melting temperature and, importantly, a significant increase in its stability in th</pubmed_abstract><journal>ACS nano</journal><pubmed_title>Metallointercalators-DNA Tetrahedron Supramolecular Self-Assemblies with Increased Serum Stability.</pubmed_title><pmcid>PMC8926058</pmcid><funding_grant_id>T32GM132029</funding_grant_id><funding_grant_id>ECCS-2025124</funding_grant_id><funding_grant_id>5T32AG029796-14</funding_grant_id><funding_grant_id>CHE-2107427</funding_grant_id><funding_grant_id>T32 GM132029</funding_grant_id><pubmed_authors>Shao F</pubmed_authors><pubmed_authors>Pierre VC</pubmed_authors><pubmed_authors>Ramakrishnam Raju MV</pubmed_authors><pubmed_authors>Srivastava K</pubmed_authors><pubmed_authors>Arriaga EA</pubmed_authors><pubmed_authors>Joaqui-Joaqui MA</pubmed_authors><pubmed_authors>Maxwell Z</pubmed_authors><pubmed_authors>Jiang M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Metallointercalators-DNA Tetrahedron Supramolecular Self-Assemblies with Increased Serum Stability.</name><description>Self-assembly of metallointercalators into DNA nanocages is a rapid and facile approach to synthesize discrete bioinorganic host/guest structures with a high load of metal complexes. Turberfield's DNA tetrahedron can accommodate one intercalator for every two base pairs, which corresponds to 48 metallointercalators per DNA tetrahedron. The affinity of the metallointercalator for the DNA tetrahedron is a function of both the structure of the intercalating ligand and the overall charge of the complex, with a trend in affinity [Ru(bpy)&lt;sub>2&lt;/sub>(dppz)]&lt;sup>2+&lt;/sup> > [Tb-DOTAm-Phen]&lt;sup>3+&lt;/sup> ≫ Tb-DOTA-Phen. Intercalation of the metal complex stabilizes the DNA tetrahedron, resulting in an increase of its melting temperature and, importantly, a significant increase in its stability in th</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2025-04-05T15:44:02.805Z</modification><creation>2025-04-05T15:44:02.805Z</creation></dates><accession>S-EPMC8926058</accession><cross_references><pubmed>35133785</pubmed><doi>10.1021/acsnano.1c10084</doi></cross_references></HashMap>