Fine-tuning the hydrophobicity of a mitochondria-targeted antioxidant.

TitleFine-tuning the hydrophobicity of a mitochondria-targeted antioxidant.
Publication TypeJournal Article
Year of Publication2004
AuthorsAsin-Cayuela, J, Manas, A-RB, James, AM, Smith, RAJ, Murphy, MP
JournalFEBS Lett
Volume571
Issue1-3
Pagination9-16
Date Published2004 Jul 30
ISSN0014-5793
KeywordsAntioxidants, Biological Transport, Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone, Intracellular Membranes, Kinetics, Mitochondria, Models, Biological, Organophosphorus Compounds, Ubiquinone
Abstract

The mitochondria-targeted antioxidant MitoQ comprises a ubiquinol moiety covalently attached through an aliphatic carbon chain to the lipophilic triphenylphosphonium cation. This cation drives the membrane potential-dependent accumulation of MitoQ into mitochondria, enabling the ubiquinol antioxidant to prevent mitochondrial oxidative damage far more effectively than untargeted antioxidants. We sought to fine-tune the hydrophobicity of MitoQ so as to control the extent of its membrane binding and penetration into the phospholipid bilayer, and thereby regulate its partitioning between the membrane and aqueous phases within mitochondria and cells. To do this, MitoQ variants with 3, 5, 10 and 15 carbon aliphatic chains were synthesised. These molecules had a wide range of hydrophobicities with octan-1-ol/phosphate buffered saline partition coefficients from 2.8 to 20000. All MitoQ variants were accumulated into mitochondria driven by the membrane potential, but their binding to phospholipid bilayers varied from negligible for MitoQ3 to essentially total for MitoQ15. Despite the span of hydrophobicites, all MitoQ variants were effective antioxidants. Therefore, it is possible to fine-tune the degree of membrane association of MitoQ and other mitochondria targeted compounds, without losing antioxidant efficacy. This indicates how the uptake and distribution of mitochondria-targeted compounds within mitochondria and cells can be controlled, thereby facilitating investigations of mitochondrial oxidative damage.

DOI10.1016/j.febslet.2004.06.045
Alternate JournalFEBS Lett.
Citation Key10.1016/j.febslet.2004.06.045
PubMed ID15280009