Synthesis and Characterization of a Novel Intrinsically Fluorescent Analog of Cholesterol with Improved Photophysical Properties

Live-cell imaging of cholesterol trafficking depends on suitable cholesterol analogs. However, existing fluorescent analogs of cholesterol either show very different physicochemical properties compared to cholesterol or demand excitation in the ultraviolet spectral region. We present a strategy to synthesize two novel intrinsically fluorescent sterol probes with a close resemblance of cholesterol. The analogs contain four conjugated double bonds in the ring system and either a keto group (probe <b>5</b>) or a hydroxy group (probe <b>6</b>) in the C3 position. The emission of <b>5</b> is in the visible range of the spectrum, i.e., red-shifted by 150 nm compared to the widely used dehydroergosterol. Together with its high multiphoton absorption, this allows for imaging of <b>5</b> on conventional microscopes, including multicolor 3D and time-lapse microscopy. Molecular dynamics simulations and nuclear magnetic resonance spectroscopy reveal that <b>5</b> can condense the fatty acyl chains of phospholipids in model membranes. In giant unilamellar vesicles, <b>5</b> partitions equally into the liquid-ordered and disordered phases. In contrast, <b>6</b> emits in the ultraviolet range and is unstable in solution, preventing its use in live-cell imaging applications. The good photophysical properties of <b>5</b> make it a suitable analogue for improved live-cell imaging of sterol transport.