<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Porchetta A</submitter><funding>Associazione Italiana per la Ricerca sul Cancro</funding><funding>Natural Sciences and Engineering Research Council of Canada</funding><funding>European Research Council</funding><funding>European Commission Directorate-General for Research and Innovation</funding><pagination>4467-71</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4498449</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(7)</volume><pubmed_abstract>Inspired by naturally occurring pH-regulated receptors, here we propose a rational approach to introduce pH-induced allostery into a wide range of DNA-based receptors. To demonstrate this we re-engineered two model DNA-based probes, a molecular beacon and a cocaine-binding aptamer, by introducing in their sequence a pH-dependent domain. We demonstrate here that we can finely tune the affinity of these model receptors and control the load/release of their specific target molecule by a simple pH change.</pubmed_abstract><journal>Nano letters</journal><pubmed_title>General Strategy to Introduce pH-Induced Allostery in DNA-Based Receptors to Achieve Controlled Release of Ligands.</pubmed_title><pmcid>PMC4498449</pmcid><funding_grant_id>14420</funding_grant_id><funding_grant_id>436381-2013</funding_grant_id><funding_grant_id>336493</funding_grant_id><pubmed_authors>Ricci F</pubmed_authors><pubmed_authors>Idili A</pubmed_authors><pubmed_authors>Porchetta A</pubmed_authors><pubmed_authors>Vallee-Belisle A</pubmed_authors></additional><is_claimable>false</is_claimable><name>General Strategy to Introduce pH-Induced Allostery in DNA-Based Receptors to Achieve Controlled Release of Ligands.</name><description>Inspired by naturally occurring pH-regulated receptors, here we propose a rational approach to introduce pH-induced allostery into a wide range of DNA-based receptors. To demonstrate this we re-engineered two model DNA-based probes, a molecular beacon and a cocaine-binding aptamer, by introducing in their sequence a pH-dependent domain. We demonstrate here that we can finely tune the affinity of these model receptors and control the load/release of their specific target molecule by a simple pH change.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jul</publication><modification>2025-04-05T09:02:43.534Z</modification><creation>2019-03-27T01:54:57Z</creation></dates><accession>S-EPMC4498449</accession><cross_references><pubmed>26053894</pubmed><doi>10.1021/acs.nanolett.5b00852</doi></cross_references></HashMap>