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J. Biol. Chem., Vol. 266, Issue 26, 17049-17059, 09, 1991
KD Vandegriff, YC Le Tellier, RM Winslow, RJ Rohlfs and JS Olson
The kinetics of O2 and CO binding to R-state human hemoglobin A0 and human
hemoglobin cross-linked between the alpha chains at Lys99 residues were
examined using ligand displacement and partial photolysis techniques.
Oxygen equilibrium curves were measured by Imai's continuous recording
method (Imai, K. (1981) Methods Enzymol. 76, 438- 449). The rate of the R
to T transition was determined after full laser photolysis of the carbon
monoxide derivative by measuring the resultant absorbance changes at an
isosbestic point for ligand binding. Chemical cross-linking caused the
R-state O2 affinity of alpha subunits to decrease 6-fold compared with
unmodified hemoglobin. This inhibition of O2 binding was the result of both
a decrease in the rate constant for ligand association and an increase in
the rate constant for dissociation. The O2 affinity of R-state beta
subunits was reduced 2- fold because of an increase in the O2 dissociation
rate constant. These changes were attributed to proximal effects on the
R-state hemes as the result of the covalent cross-link between alpha chain
G helices. This proximal strain in cross-linked hemoglobin was also
expressed as a 5- fold higher rate for the unliganded R to T allosteric
transition. The fourth O2 equilibrium binding constant, K4, measured by
kinetic techniques, could be used to analyze equilibrium curves for either
native or cross-linked hemoglobin. The resultant fitted values of the Adair
constants, a1, a2, and a3 were similar to those obtained when K4 was
allowed to vary, and the fits were of equal quality. When K4 was fixed to
the kinetically determined value, the remaining Adair constants,
particularly a3, became better defined.
Determination of the rate and equilibrium constants for oxygen and carbon monoxide binding to R-state human hemoglobin cross-linked between the alpha subunits at lysine 99
Blood Research Division, Letterman Army Institute of Research, Presidio of San Francisco, California 94219-6800.
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