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Originally published In Press as doi:10.1074/jbc.M205350200 on July 22, 2002

J. Biol. Chem., Vol. 277, Issue 39, 36787-36792, September 27, 2002
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Effects of Iron Nitrosylation on Sickle Cell Hemoglobin Solubility*

Xiuli XuDagger , Virginia L. LockamyDagger , Kejing ChenDagger , Zhi HuangDagger , Howard ShieldsDagger , S. Bruce King§, Samir K. Ballas, James S. Nichols||, Mark T. Gladwin||, Constance T. Noguchi**, Alan N. Schechter**, and Daniel B. Kim-ShapiroDagger Dagger Dagger

From the Departments of Dagger  Physics and § Chemistry, Wake Forest University, Winston-Salem, North Carolina 27109,  The Cardeza Foundation, Department of Medicine, Jefferson Medical College, Philadelphia, Pennsylvania 19107, and the || Critical Care Medicine Department, Warren G. Magnuson Clinical Center and the ** Laboratory of Chemical Biology, National Institutes of Health, Bethesda, Maryland 20892

One mechanism by which nitric oxide (NO) has been proposed to benefit patients with sickle cell disease is by reducing intracellular polymerization of sickle hemoglobin (HbS). In this study we have examined the ability of nitric oxide to inhibit polymerization by measuring the solubilizing effect of iron nitrosyl sickle hemoglobin (HbS-NO). Electron paramagnetic resonance spectroscopy was used to confirm that, as found in vivo, the primary type of NO ligation produced in our partially saturated NO samples is pentacoordinate alpha -nitrosyl. Linear dichroism spectroscopy and delay time measurements were used to confirm polymerization. Based on sedimentation studies we found that, although fully ligated (100% tetranitrosyl) HbS is very soluble, the physiologically relevant, partially ligated species do not provide a significant solubilizing effect. The average solubilizing effect of 26% NO saturation was 0.045; much less than the 0.15 calculated for the effect of 26% oxygen saturation. Given the small amounts of NO-ligated hemoglobin achievable through any kind of NO therapy, we conclude that NO therapy does not benefit patients through any direct solubilizing effect.


* This work was supported by National Institutes of Health Grant HL58091 (to D. B. K.-S.) and the Wake Forest University Catalyst award (to D. B. K.-S. and S. B. K.). Additional support was obtained from the National Institutes of Health Grant HL62198 (to S. B. K.) and the Comprehensive Sickle Cell Center Program of the Commonwealth of Pennsylvania (to S. K. B.).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Dagger Dagger To whom correspondence should be addressed. Tel.: 336-758-4993; Fax: 336-758-6142; E-mail: shapiro@wfu.edu.


Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.
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