Your browser doesn't support javascript.
loading
Design, Synthesis, and Evaluation of a Luminescent Cholesterol Mimic.
Work, Emily M; Ferraudi, Guillermo; Kiefer, Luke; Liu, Gang; Grigalunas, Michael; Bhardwaj, Atul; Kaur, Rasmin; Dempsey, Janel M; Wüstner, Daniel; Helquist, Paul; Wiest, Olaf.
Affiliation
  • Work EM; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46566, United States.
  • Ferraudi G; Radiation Research Laboratory, University of Notre Dame, Notre Dame, Indiana 46556, United States.
  • Kiefer L; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46566, United States.
  • Liu G; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46566, United States.
  • Grigalunas M; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46566, United States.
  • Bhardwaj A; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46566, United States.
  • Kaur R; Department of Biochemistry and Molecular Biology, University of Southern Denmark, DK-5230 Odense M, Denmark.
  • Dempsey JM; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46566, United States.
  • Wüstner D; Department of Biochemistry and Molecular Biology, University of Southern Denmark, DK-5230 Odense M, Denmark.
  • Helquist P; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46566, United States.
  • Wiest O; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46566, United States.
J Org Chem ; 86(2): 1612-1621, 2021 01 15.
Article in En | MEDLINE | ID: mdl-33369429
The development of new chemical tools with improved properties is essential to chemical and cell biology. Of particular interest is the development of mimics of small molecules with important cellular function that allow the direct observation of their trafficking in a cell. To this end, a novel 15-azasterol has been designed and synthesized as a luminescent cholesterol mimic for the monitoring of cholesterol trafficking. The brightness of this probe, which is ∼32-times greater than the widely used dehydroergosterol probe, is combined with resistance to photobleaching in solution and in human fibroblasts and an exceptionally large Stokes-like shift of ∼150-200 nm. The photophysical properties of the probe have been studied experimentally and computationally, suggesting an intersystem crossing to the triplet excited state with subsequent phosphorescent decay. Molecular dynamics simulations show a similar binding mode of cholesterol and the azasterol probe to NPC proteins, demonstrating the structural similarity of the probe to cholesterol.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cholesterol Limits: Humans Language: En Journal: J Org Chem Year: 2021 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cholesterol Limits: Humans Language: En Journal: J Org Chem Year: 2021 Document type: Article Affiliation country: United States Country of publication: United States