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The effects of anion transport inhibitors on structural transitions in erythrocyte membranes
Authors:Julian W. Snow  John F. Brandts  Philip S. Low
Affiliation:Department of Chemistry, University of Massachusetts, Amherst, Mass. 01003 U.S.A.
Abstract:Red blood cell membranes have been labeled with several covalent and non-covalent inhibitors of anion transport and their heat capacity profiles determined as a function of temperature. Covalent inhibitors include the amino reactive agents 4,4′-diisothiocyanostilbene-2,2′-disulfonic acid, 4-acetamido-4′-isothiocyanostilbene-2,2′-disulfonic acid, pyridoxal phosphate and 1-fluoro-2,4-dinitro benzene. The non-covalent inhibitors include several well known local anesthetics. The study was undertaken in order to identify regions of the membrane involved in anion transport. Covalent modification in all cases resulted in a large upward shift of the C transition, which is believed to involved a localized phospholipid region. Evidence is presented which indicates that Band III protein and this phospholipid region are in close physical proximity on the membrane. Addition of non-covalent inhibitors affects the membrane in either or both of two ways. In some cases, a lowering and broadening of the C transition occurs; in other the B1 and B2 transitions are altered. These latter transitions are believed to involve both phospholipid and protein, including Band III. These results may indicate that the non-covalent inhibitors produce their inhibitory effect on anion transport at least in part by interacting with membrane phospholipid.
Keywords:DADS, 4,4′-diamino-2,2′-dihydrostilbene disulfonic acid  DIDS, 4,4′-diisothiocyanostilbene-2,2′-disulfonic acid  DNFB, 1-fluoro-2,4-dinitrobenzene  SITS, 4-acetamido-4′-isothiocyanostilbene-2,2′-disulfonic acid
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