血红蛋白
玻尔效应
P50页
BETA(编程语言)
氧气
生物物理学
作者
Winston F. Moo-Penn,T. K. Hine,Mary H. Johnson,Danny L. Jue,S. Holland,S. George,Pierce Am,Michalski La,Melisenda J. McDonald
出处
期刊:Hemoglobin
[Informa]
日期:1992-01-01
卷期号:16: 35-44
被引量:5
标识
DOI:10.3109/03630269209005674
摘要
Hb Rancho Mirage was detected in a 17-year-old male in association with a mild anemia. Hemoglobin electrophoresis revealed the variant had a mobility between Hbs A and J on cellulose acetate (pH 8.6) and a mobility like Hb F on citrate agar (pH 6.4). A substitution of His→Asp was found at position 143 in the s chain, a residue that contributes to the anionic 2,3-DPG binding site in Hb. This variant exhibited normal oxygen affinity at physiologic pH and reduced affinity at alkaline pH. This suggested a subtle shift in the allosteric equilibrium due most likely to the introduction of a negative charge that stabilized the 2,3-DPG pocket. Both homotrophic (heme-heme) and heterotropic (2,3-DPG and protons) effects were reduced; this might be a consequence of an alteration in the carboxyl terminal region of the s-subunits. Although a His→Asp substitution would be considered to cause reasonable disruption of the 2,3-DPG and C-terminal conformation of the s- subunits, the properties of Hb Rancho Mirage suggest th...
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