Lipophilic ruthenium complexes with tuned cell membrane affinity and photoactivated uptake
Journal article, 2010

Ruthenium dipyridophenazine (dppz) complexes are virtually non-emissive in aqueous solutions but show strong luminescence in hydrophobic environments, making them interesting as molecular probes in cellular imaging. We show by luminescence spectroscopy that by substituting the dppz ligand with alkyl ether chains of increasing length the complexes can be tuned from preferential intercalation into DNA to insertion in model phospholipid membranes Confocal laser scanning microscopy (CLSM) on methanol fixed CHO-K1 cells show an analogous distribution in the cell, where the least hydrophobic complex exclusively stains the nucleus whereas the more hydrophobic ones seem to predominantly stain membrane structures in the cytoplasm In live cells CLSM show that initially only the more hydrophobic derivatives stain the plasma membrane However, brief further exposure to the laser light causes permeabilization of the membrane and accumulation of extracellular ruthenium complexes in internal cellular structures, similarly to the distribution found in fixed cells. (C) 2010 Elsevier B V All rights reserved

mechanism

Luminescent cellular probes

polypyridyl complex

probes

Ruthenium dipyridophenazine complex

Membrane binding

Confocal laser

Emission spectroscopy

scanning microscopy

liposome membranes

Photoactivated cellular uptake

light-switch

dna

Author

Frida Svensson

Chalmers, Chemical and Biological Engineering, Physical Chemistry

Maria Matson

Chalmers, Chemical and Biological Engineering, Physical Chemistry

M. Li

Chalmers

Per Lincoln

Chalmers, Chemical and Biological Engineering, Physical Chemistry

Biophysical Chemistry

0301-4622 (ISSN)

Vol. 149 3 102-106

Subject Categories

Biochemistry and Molecular Biology

Chemical Sciences

DOI

10.1016/j.bpc.2010.04.006

More information

Latest update

11/5/2018