Mt. Sanna et al., FUNCTIONAL ALTERATIONS IN ADULT AND FETAL HEMOGLOBIN SASSARI ASP-ALPHA-126(H9) -] HIS - THE ROLE OF ALPHA(1)ALPHA(2) CONTACT, The Journal of biological chemistry, 269(28), 1994, pp. 18338-18342
The effects of pH, organic phosphates (2,3-diphospho- glycerate), and
temperature on the functional properties of both adult and fetal hemog
lobin Sassari alpha (Asp-126 --> His) have been studied. The functiona
l properties of the adult variant are characterized by the following:
(i) an oxygen affinity higher than that of normal HbA in all the exper
imental conditions used; (ii) a dramatic reduction of homotropic inter
actions (n(50) very close to unity); and (iii) a significant decrease
of the effect of 2,3-diphosphoglycerate, which is 35% lower than that
observed on HbA. The fetal variant shows an increased oxygen affinity
compared with normal HbF and an almost abolished heme-heme interaction
. The molecular basis of these functional differences is discussed in
terms of the possible role played by the substitution of alpha (Asp-26
--> His) on the stability of the R state of the molecule due to a dec
reased interaction at the level of alpha(1) alpha(2) contact.