Assessment of chelatable mitochondrial iron by using mitochondrion-selective fluorescent iron indicators with different iron-binding affinities

Chelatable cellular iron, and chelatable mitochondrial iron in particular, has yet to be well characterized, so the overall strength with these loosely bound iron ions (presumably mainly Fe-II) are intracellularly/intramitrochondrially bound is unclear. We have previously reported the first selective mitochondrial iron indicator: rhodamine B 4-[(1,10-phenanthrolin-5-yl)amino-carbonyl]benzyl ester (RPA). With this compound as a model, we now have developed two additional mitrochondrial iron indictors with very different iron-binding affinities and have applied these to the study of the chelatable iron pool in the mitochondria of isolated rat liver cells. With the new indicator rhodamine B 4-[(2,2'-bipyridin-4-yl)aminocarbonyl]benzyl ester (RDA), with 2,2-bipyridine as a chelating unit (log beta(3) = 17.5), essentially the sane iron concentration (16.0 +/- 1.9 mu M) was determined as with RPA (log beta(3) = 21.1), despite the four orders of magnitude difference in Fe-II-binding affinity. This not only demonstrates the reliability of the procedure, but also confirms that iron complexation by these indicators does not induce any significant release of iron from the iron-storage proteins on the timescale of the experiment. In contrast, the indicator rhodamine B 4-[bis(pyridin-2-ylmethyl)-aminomethyl]benzyl ester (PIRO), with an N,N-bis(pyridin-2-ylmethyl)-amine group as chelating component (log beta(2) = 12.2), could not compete against the array of endogenous ligands. The intramitochondrial concentrations of the three indictors were determined to be in the range of 100 mu M: that is, about three orders of magnitude lower than the total concentration of endogenous compounds that might chelate iron ions. It is therefore estimated that chelatable mitochondrial iron ions are bound by endogenous ligands with apparent stability constants (log K-app) of between 9 and 14.