Kosugi H, Weinstein A S, Kikugawa K, Asakura T, Schroeder W A
Hemoglobin. 1983;7(3):205-26. doi: 10.3109/03630268309048651.
A second case of Hb York (beta 146 His leads to Pro), was discovered in a patient with polycythemia. The oxygen equilibrium curves (OEC) of red cell suspensions in a buffer (pH 7.4) at 37 degrees C revealed a biphasic curve with a P50 of only 12.5 mm Hg (normal value: 26.5 +/- 1.0 mm Hg). The purified Hb York had an extremely high affinity for oxygen with diminished cooperativity and decreased Bohr effect. The oxygen affinity was significantly reduced by inositol hexaphosphate. Molecular stability studies by mechanical shaking of various liganded forms of Hb York revealed stabilities between those of Hb A and Hb S. Isolated beta Y-subunits were more unstable than beta A-subunits at every pH examined. Hb York was 1.4 times more unstable than Hb A in 18.9% isopropanol.
在一名真性红细胞增多症患者中发现了第二例约克血红蛋白(β146 组氨酸突变为脯氨酸)。在 37℃的缓冲液(pH 7.4)中,红细胞悬液的氧平衡曲线(OEC)显示为双相曲线,P50 仅为 12.5 mmHg(正常值:26.5±1.0 mmHg)。纯化的约克血红蛋白对氧具有极高的亲和力,协同性降低,玻尔效应减弱。肌醇六磷酸可显著降低其氧亲和力。通过对各种配体形式的约克血红蛋白进行机械振荡进行分子稳定性研究,结果显示其稳定性介于血红蛋白 A 和血红蛋白 S 之间。在每个检测的 pH 值下,分离出的βY 亚基比βA 亚基更不稳定。在 18.9%的异丙醇中,约克血红蛋白的不稳定性是血红蛋白 A 的 1.4 倍。