| Literature DB >> 29805038 |
Lena Rakers1, David Grill2, Anna L L Matos2, Stephanie Wulff3, Da Wang3, Jonas Börgel1, Martin Körsgen4, Heinrich F Arlinghaus4, Hans-Joachim Galla5, Volker Gerke6, Frank Glorius7.
Abstract
Cholesterol is an essential component of most biological membranes and serves important functions in controlling membrane integrity, organization, and signaling. However, probes to follow the dynamic distribution of cholesterol in live cells are scarce and so far show only limited applicability. Herein, we addressed this problem by synthesizing and characterizing a class of versatile and clickable cholesterol-based imidazolium salts. We show that these cholesterol analogs faithfully mimic the biophysical properties of natural cholesterol in phospholipid mono- and bilayers, and that they integrate into the plasma membrane of cultured and primary human cells. The membrane-incorporated cholesterol analogs can be specifically labeled by click chemistry and visualized in live-cell imaging experiments that show a distribution and behavior comparable with that of endogenous membrane cholesterol. These results indicate that the cholesterol analogs can be used to reveal the dynamic distribution of cholesterol in live cells.Entities:
Keywords: addressable; cholesterol; imaging; imidazolium salt; ionic liquid; lipid microdomain; membrane
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Year: 2018 PMID: 29805038 DOI: 10.1016/j.chembiol.2018.04.015
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116