<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liang H</submitter><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>7260-7264</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5650247</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(39)</volume><pubmed_abstract>A promising biosensor for effectively lead (II) ion detection in practical applications was developed by constructing a Pb&lt;sup>2+&lt;/sup>-specific L-DNAzyme, the enantiomer of the natural nucleic acid-constructed D-DNAzyme. This fluorescent sensor contains the L-enzyme strand with a quencher at the 3' end, and the L-substrate strand with a fluorophore at the 5' and a quencher at the 3' ends that formed a complex. In the presence of Pb&lt;sup>2+&lt;/sup>, the L-substrate is cut into two fragments, leading to the recovery of fluorescence. The sensor shows high sensitivity and selectivity for Pb&lt;sup>2+&lt;/sup> detection with a linear response in the range of 5-100 nM and a detection limit of 3 nM in aqueous solution. Importantly, based on that L-DNAzyme consists of non-natural nucleic acids, which is i</pubmed_abstract><journal>Analytical methods : advancing methods and applications</journal><pubmed_title>Designing a Biostable L-DNAzyme for Lead(II) Ion Detection in Practical Samples.</pubmed_title><pmcid>PMC5650247</pmcid><funding_grant_id>R01 CA133086</funding_grant_id><funding_grant_id>R01 GM079359</funding_grant_id><pubmed_authors>Liang H</pubmed_authors><pubmed_authors>Cui L</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Wu C</pubmed_authors><pubmed_authors>Xie S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Designing a Biostable L-DNAzyme for Lead(II) Ion Detection in Practical Samples.</name><description>A promising biosensor for effectively lead (II) ion detection in practical applications was developed by constructing a Pb&lt;sup>2+&lt;/sup>-specific L-DNAzyme, the enantiomer of the natural nucleic acid-constructed D-DNAzyme. This fluorescent sensor contains the L-enzyme strand with a quencher at the 3' end, and the L-substrate strand with a fluorophore at the 5' and a quencher at the 3' ends that formed a complex. In the presence of Pb&lt;sup>2+&lt;/sup>, the L-substrate is cut into two fragments, leading to the recovery of fluorescence. The sensor shows high sensitivity and selectivity for Pb&lt;sup>2+&lt;/sup> detection with a linear response in the range of 5-100 nM and a detection limit of 3 nM in aqueous solution. Importantly, based on that L-DNAzyme consists of non-natural nucleic acids, which is i</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Oct</publication><modification>2025-04-26T08:37:12.54Z</modification><creation>2019-03-27T02:59:30Z</creation></dates><accession>S-EPMC5650247</accession><cross_references><pubmed>29062390</pubmed><doi>10.1039/C6AY01791F</doi><doi>10.1039/c6ay01791f</doi></cross_references></HashMap>