Sanguansermsri T, Matragoon S, Changloah L, Flatz G
Hemoglobin. 1979;3(2-3):161-74. doi: 10.3109/03630267908998911.
An abnormal hemoglobin variant was detected in a seven-year old Thai girl. The clinical and hematological pictures were indistinguishable from hemoglobin H disease. Upon cellulose acetate electrophoresis at pH 8.5 an abnormal hemoglobin variant was found together with hemoglobins A and H. The variant moved slightly behind HbF and amounted to approximately 9%. Globin chain synthesis studies of peripheral blood reticulocytes incubated with tritiated leucine revealed that the total radioactivity ratio alpha-chain + variant alpha-chain/beta-chain was 0.59, while the ratio variant alpha-chain/beta-chain was 0.12. The variant hemoglobin was somewhat unstable under heat denaturation and in the isopropanol test. Structural studies by component isolation, globin chain separation, peptide mapping and aminoacid analysis of abnormal peptides showed that the leucine residue 109 of the alpha-chain was replaced by arginine. This hemoglobin mutant has not been described before and is named Hemoglobin Suan-Dok.
在一名7岁泰国女孩中检测到一种异常血红蛋白变体。其临床和血液学表现与血红蛋白H病无法区分。在pH 8.5的醋酸纤维素电泳中,发现一种异常血红蛋白变体与血红蛋白A和H同时存在。该变体在HbF之后稍有迁移,含量约为9%。用氚标记的亮氨酸孵育外周血网织红细胞进行珠蛋白链合成研究,结果显示α链+变体α链/β链的总放射性比值为0.59,而变体α链/β链的比值为0.12。该变体血红蛋白在热变性和异丙醇试验中有些不稳定。通过组分分离、珠蛋白链分离、肽图谱分析和异常肽的氨基酸分析进行的结构研究表明,α链的第109位亮氨酸残基被精氨酸取代。这种血红蛋白突变体以前未曾有过描述,被命名为血红蛋白素攀多克。