Nakatsuji T, Shimizu K, Huisman T H
Biochim Biophys Acta. 1984 Sep 11;789(2):224-8. doi: 10.1016/0167-4838(84)90208-5.
The identification of a newly discovered gamma-chain variant is reported. This abnormal fetal hemoglobin is characterized by a Glu----Lys substitution at position 101(G3) of its gamma chain and was observed in a Caucasian baby girl. Because glutamic acid residue in position gamma 101 is involved in the alpha 1-gamma 2 chain contact, its replacement by a lysine residue results in changes in physicochemical and functional properties. The variant readily forms hybrid hemoglobins at room temperature, is mildly unstable at higher temperature, and has an increased oxygen affinity with a somewhat lower heme-heme interaction.
报道了一种新发现的γ链变体的鉴定情况。这种异常胎儿血红蛋白的特征是其γ链第101位(G3)的谷氨酸被赖氨酸取代,在一名白种女婴中被观察到。由于γ101位的谷氨酸残基参与α1-γ2链接触,被赖氨酸残基取代会导致理化和功能特性发生变化。该变体在室温下容易形成杂交血红蛋白,在较高温度下轻度不稳定,并且具有增加的氧亲和力以及稍低的血红素-血红素相互作用。