Rochette J, Boissel J P, Labie D, Wajcman H, Poyart C, Bohn B, Varet B
Nouv Rev Fr Hematol (1978). 1984;26(2):75-7.
All the high oxygen affinity variants have substitutions in regions that are crucial to hemoglobin function: mainly the alpha 1 beta 2 interface, the C-terminal end of the beta chain and the aminoacid residues involved in the 2,3 disphophoglycerate (2,3 DPG) binding site. In this report we describe a new variant with familial erythrocytosis: hemoglobin Saint-Jacques beta 140 (H18) Ala----Thr, whose main abnormality is a defect in organic phosphate binding in the central cavity between to two beta chains. This variant could not be separated from hemoglobin A by standard electrophoretic methods or by isoelectric focusing. The abnormal peptide was isolated by reverse-phase high performance liquid chromatography and the structural modification determined by manual sequencing micro-method. Functional studies on red blood cells as well as on stripped lysate showed increased oxygen affinity, normal Bohr effect, decreased heme-heme interaction and loss of the 2,3 DPG regulatory effect.
主要是α1β2界面、β链的C末端以及参与2,3-二磷酸甘油酸(2,3-DPG)结合位点的氨基酸残基。在本报告中,我们描述了一种伴有家族性红细胞增多症的新变体:血红蛋白圣雅克β140(H18)丙氨酸→苏氨酸,其主要异常是两条β链之间中心腔内有机磷酸盐结合缺陷。该变体不能通过标准电泳方法或等电聚焦与血红蛋白A分离。通过反相高效液相色谱分离出异常肽,并通过手动测序微量法确定结构修饰。对红细胞以及脱辅基裂解物的功能研究表明,氧亲和力增加、玻尔效应正常、血红素-血红素相互作用降低以及2,3-DPG调节效应丧失。