Marsh G, Marino G, Pucci P, Ferranti P, Malorni A, Kaeda J, Marsh J, Luzzatto L
Department of Haematology, North Middlesex Hospital, London, UK.
Hemoglobin. 1991;15(1-2):43-51. doi: 10.3109/03630269109072483.
Hb. Heathrow [beta 103(G5)Phe- greater than Leu] was identified in an Englishman with a life-long history of polycythemia, his father had been similarly affected. A hemoglobin variant was suspected from the high oxygen affinity of the patient's blood. The Hb Heathrow abnormal beta chain was resolved from the normal beta chain by high performance liquid chromatography, and the abnormal peptide and the amino acid replacement were identified by mass spectrometry. The corresponding base change (C- greater than G at codon 103) was demonstrated by sequence analysis of the polymerase chain reaction amplified exon 2 of the genomic beta-globin gene. This is only the third known instance of Hb Heathrow.
希思罗血红蛋白[β103(G5)苯丙氨酸→亮氨酸]在一名有长期红细胞增多症病史的英国男性中被发现,他的父亲也有类似症状。由于患者血液的高氧亲和力,怀疑存在血红蛋白变体。通过高效液相色谱法将希思罗血红蛋白异常的β链与正常β链分离,并通过质谱法鉴定异常肽段和氨基酸替代情况。通过对聚合酶链反应扩增的基因组β珠蛋白基因外显子2进行序列分析,证实了相应的碱基变化(密码子103处C→G)。这是希思罗血红蛋白已知的第三个病例。