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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
Effects of Iron Nitrosylation on Sickle Cell Hemoglobin
Solubility*
Xiuli
Xu ,
Virginia L.
Lockamy ,
Kejing
Chen ,
Zhi
Huang ,
Howard
Shields ,
S. Bruce
King§,
Samir K.
Ballas¶,
James S.
Nichols ,
Mark T.
Gladwin ,
Constance T.
Noguchi**,
Alan N.
Schechter**, and
Daniel B.
Kim-Shapiro 
From the Departments of 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 -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.

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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