<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bay C</submitter><funding>Deutsche Forschungsgemeinschaft</funding><funding>Faculty of Medicine of Heidelberg University</funding><pagination>3637</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8998838</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(7)</volume><pubmed_abstract>The solute carrier L-type amino acid transporter 1 (LAT-1/SLC7A5) is a viable target for drug delivery to the central nervous system (CNS) and tumors due to its high abundance at the blood-brain barrier and in tumor tissue. LAT-1 is only localized on the cell surface as a heterodimer with CD98, which is not required for transporter function. To support future CNS drug-delivery development based on LAT-1 targeting, we established an ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) assay for stable isotopically labeled leucine ([&lt;sup>13&lt;/sup>C&lt;sub>6&lt;/sub>, &lt;sup>15&lt;/sup>N]-L-leucine), with a dynamic range of 0.1-1000 ng/mL that can be applied for the functional testing of LAT-1 activity when combined with specific inhibitors and, consequently, the LAT-1 inhibition</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Functional Characterization of the Solute Carrier LAT-1 (SLC7A5/SLC2A3) in Human Brain Capillary Endothelial Cells with Rapid UPLC-MS/MS Quantification of Intracellular Isotopically Labelled L-Leucine.</pubmed_title><pmcid>PMC8998838</pmcid><funding_grant_id>SFB 1389</funding_grant_id><funding_grant_id>Physician Scientist Program</funding_grant_id><pubmed_authors>Weiss J</pubmed_authors><pubmed_authors>Sauter M</pubmed_authors><pubmed_authors>Bay C</pubmed_authors><pubmed_authors>Haefeli WE</pubmed_authors><pubmed_authors>Bajraktari-Sylejmani G</pubmed_authors><pubmed_authors>Burhenne J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Functional Characterization of the Solute Carrier LAT-1 (SLC7A5/SLC2A3) in Human Brain Capillary Endothelial Cells with Rapid UPLC-MS/MS Quantification of Intracellular Isotopically Labelled L-Leucine.</name><description>The solute carrier L-type amino acid transporter 1 (LAT-1/SLC7A5) is a viable target for drug delivery to the central nervous system (CNS) and tumors due to its high abundance at the blood-brain barrier and in tumor tissue. LAT-1 is only localized on the cell surface as a heterodimer with CD98, which is not required for transporter function. To support future CNS drug-delivery development based on LAT-1 targeting, we established an ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) assay for stable isotopically labeled leucine ([&lt;sup>13&lt;/sup>C&lt;sub>6&lt;/sub>, &lt;sup>15&lt;/sup>N]-L-leucine), with a dynamic range of 0.1-1000 ng/mL that can be applied for the functional testing of LAT-1 activity when combined with specific inhibitors and, consequently, the LAT-1 inhibition</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-04T09:53:22.056Z</modification><creation>2024-11-14T23:48:30.243Z</creation></dates><accession>S-EPMC8998838</accession><cross_references><pubmed>35408997</pubmed><doi>10.3390/ijms23073637</doi></cross_references></HashMap>