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Labeling of Phosphatidylinositol Lipid Products in Cells through Metabolic Engineering by Using a Clickable myo-Inositol Probe.
Ricks, Tanei J; Cassilly, Chelsi D; Carr, Adam J; Alves, Daiane S; Alam, Shahrina; Tscherch, Kathrin; Yokley, Timothy W; Workman, Cameron E; Morrell-Falvey, Jennifer L; Barrera, Francisco N; Reynolds, Todd B; Best, Michael D.
Afiliação
  • Ricks TJ; Department of Chemistry, University of Tennessee, 1420 Circle Park Drive, Knoxville, TN, 37996, USA.
  • Cassilly CD; Department of Microbiology, University of Tennessee, 1414 Cumberland Avenue, Knoxville, TN, 37996-0840, USA.
  • Carr AJ; Department of Chemistry, University of Tennessee, 1420 Circle Park Drive, Knoxville, TN, 37996, USA.
  • Alves DS; Department of Biochemistry and Cellular and Molecular Biology, University of Tennessee, 1414 Cumberland Avenue, Knoxville, TN, 37996-0840, USA.
  • Alam S; Department of Chemistry, University of Tennessee, 1420 Circle Park Drive, Knoxville, TN, 37996, USA.
  • Tscherch K; Department of Chemistry, University of Tennessee, 1420 Circle Park Drive, Knoxville, TN, 37996, USA.
  • Yokley TW; Department of Chemistry, University of Tennessee, 1420 Circle Park Drive, Knoxville, TN, 37996, USA.
  • Workman CE; Department of Chemistry, University of Tennessee, 1420 Circle Park Drive, Knoxville, TN, 37996, USA.
  • Morrell-Falvey JL; Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, 37831-6445, USA.
  • Barrera FN; Department of Biochemistry and Cellular and Molecular Biology, University of Tennessee, 1414 Cumberland Avenue, Knoxville, TN, 37996-0840, USA.
  • Reynolds TB; Department of Microbiology, University of Tennessee, 1414 Cumberland Avenue, Knoxville, TN, 37996-0840, USA.
  • Best MD; Department of Chemistry, University of Tennessee, 1420 Circle Park Drive, Knoxville, TN, 37996, USA.
Chembiochem ; 20(2): 172-180, 2019 01 18.
Article em En | MEDLINE | ID: mdl-30098105
ABSTRACT
Phosphatidylinositol (PI) lipids control critical biological processes, so aberrant biosynthesis often leads to disease. As a result, the capability to track the production and localization of these compounds in cells is vital for elucidating their complex roles. Herein, we report the design, synthesis, and application of clickable myo-inositol probe 1 a for bioorthogonal labeling of PI products. To validate this platform, we initially conducted PI synthase assays to show that 1 a inhibits PI production in vitro. Fluorescence microscopy experiments next showed probe-dependent imaging in T-24 human bladder cancer and Candida albicans cells. Growth studies in the latter showed that replacement of myo-inositol with probe 1 a led to an enhancement in cell growth. Finally, fluorescence-based TLC analysis and mass spectrometry experiments support the labeling of PI lipids. This approach provides a promising means for tracking the complex biosynthesis and trafficking of these lipids in cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfatidilinositóis / Engenharia Metabólica / Corantes Fluorescentes / Inositol Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfatidilinositóis / Engenharia Metabólica / Corantes Fluorescentes / Inositol Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article