A Basis of the Stomatocytoses of Erythrocytes by 1-Chloro-2, 4-Dinitrobenzene and Other Electrophilic Reagents

Pierre Wong*
LCP, Section Théorique,Canada

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© Pierre Wong; Licensee Bentham Open.

open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License ( which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.

* Address correspondence to this author at the Laboratoire de Chimie des Protéines, Section Théorique, 3415 Aylmer, Montréal, Québec, Canada H2X 2B4; Tel: 514-849-1550; E-mail:


On bases of previous observations on the band 3 anion exchange inhibition by the electrophilic reagent 1-fluoro-2,4-dinitrobenzene in resealed ghosts and a previously proposed band 3-based mechanism of control of the erythrocyte shape, it is suggested that stomatocytoses by 1-chloro-2,4-dinitrobenzene and other electrophilic reagents are due to an inhibition of the band 3 anion exchange by a covalent modification of Lys 539, one of the two lysine intramolecularly cross-linked by impermeant 4,4’-diisothiocyanodihydrostilbene-2,2’- disulfonic acid, a band 3 anion exchange potent inhibitor. Attempts to explain these stomatocytoses led to explain the echinocytosis and competitive inhibition of band 3 anion exchange by stilbenedisulfonic acid derivatives and the reversal of the echinocytosis by 2,4-dinitrophenol by one stomatocytogenic of the electrophilic reagents. The inference on stomatocytoses by electrophilic reagents is of interest since stomatocytogenic and echinocytogenic by amphiphiles are perceived to interact non-covalently with the membrane and that they can be clinically relevant.

Keywords: Band 3, echinocytosis, 1-fluoro-2, -dinitrobenzene, glucose, stilbenedisulfonic acid, stomatocytosis, skeleton..