| Literature DB >> 33369429 |
Emily M Work1, Guillermo Ferraudi2, Luke Kiefer1, Gang Liu1, Michael Grigalunas1, Atul Bhardwaj1, Rasmin Kaur3, Janel M Dempsey1, Daniel Wüstner3, Paul Helquist1, Olaf Wiest1.
Abstract
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.Entities:
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Year: 2020 PMID: 33369429 PMCID: PMC8126345 DOI: 10.1021/acs.joc.0c02460
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354