Zeng Y T, Ren Z R, Chen M J, Zhao J Q, Qiu X K, Huang S Z
Laboratory of Medical Genetics, Shanghai Children's Hospital, China.
Br J Haematol. 1987 Oct;67(2):221-3. doi: 10.1111/j.1365-2141.1987.tb02330.x.
A 34-year-old woman patient was found to have a chronic hereditary haemolytic anaemia. No abnormal haemoglobin band was detected by conventional electrophoresis, but a slow beta chain could be separated on urea-carboxymethyl cellulose chromatography. Investigations of the patient's haemoglobin revealed an unstable component. Analyses of chemical structure, including isolation and TPCK trypsin digestion of the abnormal globin chain. HPL chromatography, amino acid composition as well as sequence determination of the abnormal peptide, indicated that a glutamine was replaced by a proline at position beta 131 (H9). Biosynthesis studies demonstrated a normal rate of synthesis but relatively fast degradation of the mutant beta chain. The new variant is named as Hb Shanghai according to the place where it was discovered.
一名34岁女性患者被诊断患有慢性遗传性溶血性贫血。常规电泳未检测到异常血红蛋白条带,但在尿素-羧甲基纤维素色谱上可分离出一条缓慢的β链。对患者血红蛋白的研究发现了一种不稳定成分。对化学结构进行分析,包括异常珠蛋白链的分离和TPCK胰蛋白酶消化、高效液相色谱、氨基酸组成以及异常肽的序列测定,结果表明在β131(H9)位的谷氨酰胺被脯氨酸取代。生物合成研究表明,突变型β链的合成速率正常,但降解相对较快。根据发现地,这个新变体被命名为血红蛋白上海(Hb Shanghai)。