<HashMap><database>biostudies-literature</database><scores/><additional><submitter>June CM</submitter><funding>NIAID NIH HHS</funding><pagination>70-4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4167909</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>463</volume><pubmed_abstract>By reacting fluorescein isothiocyanate with meropenem, we have prepared a carbapenem-based fluorescent ?-lactam. Fluorescein-meropenem binds both penicillin-binding proteins and ?-lactam sensors and undergoes a typical acylation reaction in the active site of these proteins. The probe binds the class D carbapenemase OXA-24/40 with close to the same affinity as meropenem and undergoes a complete catalytic hydrolysis reaction. The visible light excitation and strong emission of fluorescein render this molecule a useful structure-function probe through its application in sodium dodecyl sulfate-polyacrylamide gel electrophoresis assays as well as solution-based kinetic anisotropy assays. Its classification as a carbapenem ?-lactam and the position of its fluorescent modification render it a useful complement to other fluorescent ?-lactams, most notably Bocillin FL. In this study, we show the utility of fluorescein-meropenem by using it to detect mutants of OXA-24/40 that arrest at the acyl-intermediate state with carbapenem substrates but maintain catalytic competency with penicillin substrates.</pubmed_abstract><journal>Analytical biochemistry</journal><pubmed_title>A fluorescent carbapenem for structure function studies of penicillin-binding proteins, ?-lactamases, and ?-lactam sensors.</pubmed_title><pmcid>PMC4167909</pmcid><funding_grant_id>R01AI072219</funding_grant_id><funding_grant_id>R01 AI063517</funding_grant_id><funding_grant_id>R01AI063517</funding_grant_id><funding_grant_id>R15 AI082416</funding_grant_id><funding_grant_id>R01 AI072219</funding_grant_id><funding_grant_id>R15AI082416</funding_grant_id><pubmed_authors>Ulberg LS</pubmed_authors><pubmed_authors>Vaughan RM</pubmed_authors><pubmed_authors>Leonard DA</pubmed_authors><pubmed_authors>June CM</pubmed_authors><pubmed_authors>Witucki LA</pubmed_authors><pubmed_authors>Bonomo RA</pubmed_authors></additional><is_claimable>false</is_claimable><name>A fluorescent carbapenem for structure function studies of penicillin-binding proteins, ?-lactamases, and ?-lactam sensors.</name><description>By reacting fluorescein isothiocyanate with meropenem, we have prepared a carbapenem-based fluorescent ?-lactam. Fluorescein-meropenem binds both penicillin-binding proteins and ?-lactam sensors and undergoes a typical acylation reaction in the active site of these proteins. The probe binds the class D carbapenemase OXA-24/40 with close to the same affinity as meropenem and undergoes a complete catalytic hydrolysis reaction. The visible light excitation and strong emission of fluorescein render this molecule a useful structure-function probe through its application in sodium dodecyl sulfate-polyacrylamide gel electrophoresis assays as well as solution-based kinetic anisotropy assays. Its classification as a carbapenem ?-lactam and the position of its fluorescent modification render it a useful complement to other fluorescent ?-lactams, most notably Bocillin FL. In this study, we show the utility of fluorescein-meropenem by using it to detect mutants of OXA-24/40 that arrest at the acyl-intermediate state with carbapenem substrates but maintain catalytic competency with penicillin substrates.</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Oct</publication><modification>2020-10-31T08:51:21Z</modification><creation>2019-03-27T01:35:54Z</creation></dates><accession>S-EPMC4167909</accession><cross_references><pubmed>25058926</pubmed><doi>10.1016/j.ab.2014.07.012</doi></cross_references></HashMap>