Bosisio A B, Rochette J, Wajcman H, Gianazza E, Righetti P G
J Chromatogr. 1985 Aug 23;330(2):299-306. doi: 10.1016/s0021-9673(01)81986-5.
A method is described for separating haemoglobin (Hb) E (beta 26 Gly----Lys) from Hb A2 (a normal minor Hb component in adult blood). The technique allows the distinction between subjects carrying beta-thalassaemia trait and patients who are simultaneously alpha-thalassaemic and heterozygous for Hb E, the standard electrophoretic pattern often being similar in these two circumstances. Complete separation between Hb E and Hb A2 (2 mm empty space in between) is obtained by isoelectric focusing in immobilized pH gradients in an ultra-narrow pH 7.55-7.65 gradient. The apparent pI values of the two species (at 10 degrees C and at an average ionic strength of 5.6 mequiv. l-1) have been calculated to be 7.603 for Hb E and 7.607 for Hb A2. Thus, the system reported here affords a resolution of at least 0.004 pH unit.
本文描述了一种从成人血液中的正常次要血红蛋白成分血红蛋白A2(Hb A2)中分离血红蛋白E(Hb E,β26 Gly→Lys)的方法。该技术能够区分携带β地中海贫血特征的个体与同时患有α地中海贫血且为Hb E杂合子的患者,这两种情况下的标准电泳图谱通常相似。通过在固定化pH梯度中进行等电聚焦,在超窄的pH 7.55 - 7.65梯度下可实现Hb E和Hb A2的完全分离(两者之间有2毫米的空白间隔)。已计算出这两种血红蛋白在10℃、平均离子强度为5.6毫当量·升⁻¹时的表观等电点(pI)值,Hb E为7.603,Hb A2为7.607。因此,本文报道的系统分辨率至少为0.004个pH单位。