Coordination and Fluorescence of the Intracellular Zn2+ Probe [2-methyl-8-(4-Toluenesulfonamido)-6-quinolyloxy]acetic Acid (Zinquin A) in Ternary Zn2+ Complexes
journal contributionposted on 11.03.2003, 00:00 by Kym M. Hendrickson, Jason P. Geue, Oska Wyness, Stephen F. Lincoln, A. David Ward
A potentiometric study of the coordination of the fluorophore, 2-methyl-8-(4-toluenesulfonamido)-6-quinolyloxyacetic acid, 1LH2 (the intracellular Zn2+ probe, Zinquin A) in its deprotonated form, 1L2-, in Zn2+ ternary complexes, [ZnnL1L]n (where n is the charge of nL) at 298.2 K in 50% aqueous ethanol (v/v) and I = 0.10 (NaClO4), shows that the formation of [ZnnL1L]n from [ZnnL](2+n)+ is characterized by log(K5/dm3 mol-1) = 8.23 ± 0.05, 4.36 ± 0.18, 8.45 ± 0.10, 10.00 ± 0.06, 11.53 ± 0.06 and 5.92 ± 0.15, respectively, where nL = 2L − 6L and 7L3- are 1,4,7,10-tetraazacyclododecane, 1,4,8,11-tetraazacyclotetradecane, 1,4,7-triazacyclononane, 1,5,9-triazacyclododecane, tris(2-aminoethyl)amine and nitrilotriacetate, respectively, and K5 is the stepwise complexation constant. Dissociation of a hydroxo proton from triethanolamine, 8L, occurs in the formation of [Zn8LH-1]+ that subsequently forms [Zn8LH-11L]- for which log(K5/dm3 mol-1) = 9.87 ± 0.08. The variation of K5 and the 5-fold variation of quantum yield of 1L2- as its coordination environment changes in Zn2+ ternary complexes are discussed with reference to the use of 1L2- in the detection of intracellular Zn2+.