TY - JOUR
T1 - PARTIAL RESTORATION OF NORMAL FUNCTIONAL PROPERTIES IN CARBOXYPEPTIDASE A DIGESTED HEMOGLOBIN
AU - B. o. n. a. v. e. n. t. J, N
AU - B. o. n. a. v. e. n. t. C, N
AU - Brunori, M
AU - Antonini, E
AU - Wyman, J
AU - Giardina, Bruno
PY - 1972
Y1 - 1972
N2 - In the absence of organic phosphates human hemoglobin A digested with carboxypeptidase A (des His, Tyr β) has high ligand affinity, a greatly reduced Bohr effect, and no heme-heme interaction. Under these conditions, it shows the simple, homogeneous ligand-binding kinetics characteristic of noncooperative heme proteins in which the high combination velocity for both O2 and CO accounts, to a larger extent, for the increased affinity for both these ligands.
Addition of inositol hexaphosphate dramatically alters the functional properties of this digested hemoglobin. The Bohr effect is greatly increased, and at neutral pH the protein shows significant, though still reduced, heme-heme interaction, together with a 5-fold decrease in affinity. In the presence of saturating amounts of the organic phosphate, the value of n is pH dependent, dropping from 1.9 at pH 5.8 to 1.3 at pH 8.6. After inositol hexaphosphate addition, the combination of the deoxy form of the digested hemoglobin with CO is 10-times slower than that observed in the absence of the inorganic phosphate; also the combination with CO after flash photolysis is biphasic and is similar, in many respects, to that observed for unmodified hemoglobin. Besides these functional changes, addition of inositol hexaphosphate to the modified deoxyhemoglobin results in an increase in the extinction coefficient at 430 nm similar to that observed on mixing the isolated α and β chains of normal hemoglobin. The results are consistent with the idea that inositol hexaphosphate shifts an equilibrium between high- and low-affinity forms of the protein.
AB - In the absence of organic phosphates human hemoglobin A digested with carboxypeptidase A (des His, Tyr β) has high ligand affinity, a greatly reduced Bohr effect, and no heme-heme interaction. Under these conditions, it shows the simple, homogeneous ligand-binding kinetics characteristic of noncooperative heme proteins in which the high combination velocity for both O2 and CO accounts, to a larger extent, for the increased affinity for both these ligands.
Addition of inositol hexaphosphate dramatically alters the functional properties of this digested hemoglobin. The Bohr effect is greatly increased, and at neutral pH the protein shows significant, though still reduced, heme-heme interaction, together with a 5-fold decrease in affinity. In the presence of saturating amounts of the organic phosphate, the value of n is pH dependent, dropping from 1.9 at pH 5.8 to 1.3 at pH 8.6. After inositol hexaphosphate addition, the combination of the deoxy form of the digested hemoglobin with CO is 10-times slower than that observed in the absence of the inorganic phosphate; also the combination with CO after flash photolysis is biphasic and is similar, in many respects, to that observed for unmodified hemoglobin. Besides these functional changes, addition of inositol hexaphosphate to the modified deoxyhemoglobin results in an increase in the extinction coefficient at 430 nm similar to that observed on mixing the isolated α and β chains of normal hemoglobin. The results are consistent with the idea that inositol hexaphosphate shifts an equilibrium between high- and low-affinity forms of the protein.
KW - HEMOGLOBIN
KW - HEMOGLOBIN
UR - http://hdl.handle.net/10807/5771
U2 - 10.1073/pnas.69.8.2174
DO - 10.1073/pnas.69.8.2174
M3 - Article
SN - 0027-8424
VL - 69
SP - 2174-2174-\&
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
ER -