<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bae SW</submitter><funding>NIBIB NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><funding>National Science Foundation</funding><pagination>e1800353</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9533696</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(2)</volume><pubmed_abstract>DNA aptamers are integrated into synthetic hydrogel networks with the aim of creating hydrogels that undergo volume changes when exposed to target molecules. Specifically, single-stranded DNA aptamers in cDNA-bound, extended state are incorporated into hydrogel networks as cross-links, so that the nanoscale conformational change of DNA aptamers upon binding to target molecules will induce macroscopic volume decreases of hydrogels. Hydrogels incorporating adenosine triphosphate (ATP)-binding aptamers undergo controllable volume decreases of up to 40.3 ± 4.6% when exposed to ATP, depending on the concentration of DNA aptamers incorporated in the hydrogel network, temperature, and target molecule concentration. Importantly, this approach can be generalized to aptamer sequences with distinct b</pubmed_abstract><journal>Macromolecular bioscience</journal><pubmed_title>Dynamic, Bioresponsive Hydrogels via Changes in DNA Aptamer Conformation.</pubmed_title><pmcid>PMC9533696</pmcid><funding_grant_id>R01 HL093282</funding_grant_id><funding_grant_id>R21EB016381</funding_grant_id><funding_grant_id>DMR #1306482</funding_grant_id><funding_grant_id>R01HL093282</funding_grant_id><funding_grant_id>R21 EB016381</funding_grant_id><pubmed_authors>Lee JS</pubmed_authors><pubmed_authors>Harms VM</pubmed_authors><pubmed_authors>Bae SW</pubmed_authors><pubmed_authors>Murphy WL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dynamic, Bioresponsive Hydrogels via Changes in DNA Aptamer Conformation.</name><description>DNA aptamers are integrated into synthetic hydrogel networks with the aim of creating hydrogels that undergo volume changes when exposed to target molecules. Specifically, single-stranded DNA aptamers in cDNA-bound, extended state are incorporated into hydrogel networks as cross-links, so that the nanoscale conformational change of DNA aptamers upon binding to target molecules will induce macroscopic volume decreases of hydrogels. Hydrogels incorporating adenosine triphosphate (ATP)-binding aptamers undergo controllable volume decreases of up to 40.3 ± 4.6% when exposed to ATP, depending on the concentration of DNA aptamers incorporated in the hydrogel network, temperature, and target molecule concentration. Importantly, this approach can be generalized to aptamer sequences with distinct b</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Feb</publication><modification>2025-04-19T17:36:15.254Z</modification><creation>2025-04-19T17:36:15.254Z</creation></dates><accession>S-EPMC9533696</accession><cross_references><pubmed>30565861</pubmed><doi>10.1002/mabi.201800353</doi></cross_references></HashMap>