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PMID: 11684095 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cardiolipin binds nonyl acridine orange by aggregating the dye at exposed hydrophobic domains on bilayer surfaces.

FEBS letters ·Vol. 507 ·No. 2 ·2001-10-26 ·Pages 187-90

Mileykovskaya E, Dowhan W, Birke RL, Zheng D, Lutterodt L, Haines TH

Abstract

10-N-Nonyl acridine orange (NAO) has been used at low concentrations as a fluorescent indicator for cardiolipin (CL) in membranes and bilayers. The mechanism of its selective fluorescence in the presence of CL, and not any other phospholipids, is not understood. The dye might recognize CL by its high pK (pK(2)>8.5). To investigate that, we established that NAO does not exhibit a pK in a pH range between 2.3 and 10.0. A second explanation is that the dye aggregates at hydrophobic domains on bilayers exposed by the CL. We found that a similar spectral shift occurs in the absence of CL in a concentrated solution of the dye in methanol and in the solid state. A model is proposed in which the nonyl group inserts in the bilayer at the hydrophobic surface generated by the presence of four chains on the phospholipid.

MeSH Terms
Acridine Orange/analogs & derivatives,metabolism Binding Sites Cardiolipins/metabolism Fluorescent Dyes/metabolism Hydrophobic and Hydrophilic Interactions Lipid Bilayers/metabolism Spectrometry, Fluorescence/methods
Chemicals
Cardiolipins Fluorescent Dyes Lipid Bilayers N(10)-nonylacridine orange Acridine Orange
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Mileykovskaya E
University of Texas-Houston Medical School, USA.
Dowhan W
Birke R L
Zheng D
Lutterodt L
Haines T H
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
2001-10-26
Pages
187-90
Language
English
Region
England
NLM ID
0155157
Subset
IM
Grants
NIGMS NIH HHS · GM 54272 · United States
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