Gilbert A T, Fleming P J, Sumner D R, Hughes W G, Ip F, Kwan Y L, Holland R A
Hematology Department, Westmead Hospital, N.S.W., Australia.
Hemoglobin. 1988;12(2):149-61. doi: 10.3109/03630268808998021.
A new beta-chain hemoglobin variant, Hb Randwick [beta 15(A12)Trp----Gly] was detected in a 43-year-old female of Northern Italian parentage. During investigation for possible diabetes, mild red cell changes were noted and hemoglobin electrophoresis studies were requested. Independently, her sister's assessment had resulted in similar investigations. The most prominent findings were numerous "Hb H"-like inclusions and a positive isopropanol stability test. The hemoglobin variant separated poorly towards the anode at pH 9.2 and the level was estimated to be between 48-50% of the total hemoglobin. The variant beta-chain was partially purified by column chromatography, and its tryptic peptides fractionated by high performance liquid chromatography. Amino acid analysis and sequence data indicated that the tryptophan at residue 15 (A12) had been substituted by a glycine residue. Further study has indicated that eight other family members are heterozygous for the variant; they are clinically normal with no evidence of splenomegaly or history of jaundice, although four of them showed a mild reticulocytosis.
在一位祖籍意大利北部的43岁女性中检测到一种新的β链血红蛋白变异体,即Hb Randwick [β15(A12)色氨酸→甘氨酸]。在对可能的糖尿病进行调查期间,发现了轻度红细胞变化,并要求进行血红蛋白电泳研究。此外,她姐姐的检查结果也导致了类似的研究。最显著的发现是大量类似“Hb H”的包涵体和异丙醇稳定性试验呈阳性。在pH 9.2时,该血红蛋白变异体向阳极的分离效果较差,其水平估计占总血红蛋白的48%至50%。通过柱色谱法对变异的β链进行了部分纯化,并通过高效液相色谱法对其胰蛋白酶肽进行了分级分离。氨基酸分析和序列数据表明,第15位(A12)的色氨酸被甘氨酸残基取代。进一步研究表明,其他八名家族成员为该变异体的杂合子;他们在临床上正常,没有脾肿大或黄疸病史的证据,尽管其中四人表现出轻度网织红细胞增多。