Calcein as a fluorescent probe for ferric iron - Application to iron nutrition in plant cells

The recent use of calcein (CA) as a fluorescent probe for cellular iron has been shown to reflect the nutritional status of iron in mammalian cells (B reuer, W, Epsztejn, S,, and Cabantchik, Z, I. (1995) J, Biol. Chem. 270, 24 209-24215), CA was claimed to be a chemosensor for iron(II), to measure the labile iron pool and the concentration of cellular free iron(II), We first study here the thermodynamic and kinetic properties of iron binding by CA. Chelation of a first iron(III) involves one aminodiacetic arm and a phenol . The overall stability constant log beta(111) of Fe(III)CAH is 33.9, The f ree metal ion concentration is pFe(III) = 20.3, A (Fe-III)(2) CA complex ca n be formed, A reversible iron(III) exchange from Fe(III)CAH to citrate and nitrilotriacetic acid is evidenced when these ligands are present in large excess. The kinetics of iron(III) exchange by CA is compatible with metabo lic studies. The low reduction potential of Fe(III)CAH shows that the ferri c form is highly stabilized. CA fluorescence is quenched by 85% after Fe-II I chelation but by only 20% using Fe-II. Real time iron nutrition by Arabid opsis thaliana cells has been measured by fluorimetry, and the iron buffer Fe(III)CAH + CA was used as source of iron. As a siderophore, Fe(III)CAH pr omotes cell growth and regreening of iron-deficient cells more rapidly than Fe(III)EDTA. We conclude that CA is a good chemosensor for iron(III) in ce lls and biological fluids, but not for Fe(II), We discuss the interest of q uantifying iron buffers in biochemical studies of iron, in vitro as well as in cells.