The eosin-5-maleimide binding site on human erythrocyte band 3: investigation of membrane sidedness and location of charged residues by triplet state quenching.

The triplet probe eosin-5-maleimide (EMA) is a specific inhibitor of anion transport mediated by the erythrocyte membrane protein, band 3. It was previously shown that the eosin moiety is located close to the anion binding site when EMA is covalently bound to band 3 [Pan, R.-j., and Cherry, R. J. (1995) Biochemistry 34, 4880-4888]. In the present study the electrostatic properties and membrane sidedness of the EMA binding site of band 3 were further investigated by triplet state quenching. A series of stable nitroxyl free radicals, which are characterized by different charges, and I- were used as the quenchers. Time-resolved laser spectroscopy was employed to measure the triplet lifetime of EMA. It was found that the quenching reaction between the quenchers and band 3-bound EMA follows a linear Stern-Volmer plot. The quenching rate constants (Kq) of the quenchers are in the order of NH3+-TEMPO (Kq = 6.34 x 10(6) M-1 s-1) > TEMPO-Choline+ (Kq = 2.18 x 10(6) M-1 s-1) > TEMPO (Kq = 1.13 x 10(6) M-1 s-1) > I- (Kq = 2.46 x 10(5) M-1 s-1) > pyrroline-COO- (Kq = 2.18 x 10(4) M-1 s-1). Experiments with resealed ghosts and inside-out vesicles revealed that negatively charged quenchers can only access the EMA binding site from the extracellular side of the membrane while the positively charged quenchers acted from the cytoplasmic side. The ionic strength dependence of the quenching rate constants and the effects of pH on the quenching reaction were also studied. For both TEMPO-Choline+ and I-, the Kq values decreased as the ionic strength increased, but quenching by TEMPO was independent of the ionic strength variation over the same range. It was also found that at lower pH, the I- quenching rate constant increases but the TEMPO-choline+ quenching rate constant decreases. In both cases, the dependence of quenching on pH exhibited an apparent pKa of about 6.5, which suggests the involvement of one or more histidine residues. This notion gained further support from the finding that modification of His residues of band 3 by DEPC reduced I- quenching at pH 6. On the basis of these results, it is proposed that eosin is located in the anion transport channel such that it is accessible from both sides of the membrane. Histidine residues, which have previously been proposed to lie in the anion channel, probably are located on either side of the eosin probe where they contribute to electrostatic interactions which determine the Kq values for the charged quenchers.