Synthesis and biological evaluation of cationic TopFluor cholesterol analogues

Bioorg Chem. 2021 Dec:117:105410. doi: 10.1016/j.bioorg.2021.105410. Epub 2021 Oct 6.

Abstract

Cholesterol is not only a major component of the cell membrane, but also plays an important role in a wide range of biological processes and pathologies. It is therefore crucial to develop appropriate tools for visualizing intracellular cholesterol transport. Here, we describe new cationic analogues of BODIPY-Cholesterol (TopFluor-Cholesterol, TF-Chol), which combine a positive charge on the sterol side chain and a BODIPY group connected via a C-4 linker. In contrast to TF-Chol, the new analogues TF-1 and TF-3 possessing acetyl groups on the A ring (C-3 position on steroid) internalized much faster and displayed slightly different levels of intracellular localization. Their applicability for cholesterol monitoring was indicated by the fact that they strongly label compartments with accumulated cholesterol in cells carrying a mutation of the Niemann-Pick disease-associated cholesterol transporter, NPC1.

Keywords: Cholesterol transport; Fluorescence imaging; Sterol; TopFluor cholesterol analogues; Trafficking disorders.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Transport
  • Boron Compounds / analysis*
  • Boron Compounds / chemical synthesis
  • Boron Compounds / chemistry
  • Boron Compounds / metabolism
  • Cell Line
  • Cholesterol / analogs & derivatives
  • Cholesterol / analysis*
  • Cholesterol / chemical synthesis
  • Cholesterol / metabolism
  • Humans
  • Optical Imaging

Substances

  • 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
  • Boron Compounds
  • Cholesterol