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通过高效液相色谱法分离正常和异常的α、β、γ及δ血红蛋白链的胰蛋白酶肽段。

Separation of tryptic peptides of normal and abnormal alpha, beta, gamma, and delta hemoglobin chains by high-performance liquid chromatography.

作者信息

Wilson J B, Lam H, Pravatmuang P, Huisman T H

出版信息

J Chromatogr. 1979 Nov 21;179(2):271-90. doi: 10.1016/s0021-9673(00)83830-3.

Abstract

High-performance liquid chromatography (HPLC) was used to separate tryptic peptides of the normal alpha, beta, gamma, and delta chains of human hemoglobins A, F, and A2 and of the abnormal chains of 25 hemoglobin variants. In addition, the separation of chymotryptic peptides of the oxidized core of the normal alpha chain by HPLC was evaluated. HPLC has several advantages over conventional methods used for the separation of proteolytic fragments of hemoglobin chains. The method is fast, and reproducible, and requires only small quantities of material. Several peptides are eluted as single zones, thus eliminating the need of rechromatography for further purification. Characteristic changes in the elution pattern of the peptides often indicate specific modifications.

摘要

高效液相色谱法(HPLC)用于分离人血红蛋白A、F和A2的正常α、β、γ和δ链以及25种血红蛋白变体的异常链的胰蛋白酶肽段。此外,还评估了通过HPLC分离正常α链氧化核心的糜蛋白酶肽段。与用于分离血红蛋白链蛋白水解片段的传统方法相比,HPLC有几个优点。该方法快速、可重复,只需要少量材料。几种肽以单个区带洗脱,因此无需再进行色谱分离以进一步纯化。肽段洗脱模式的特征性变化通常表明存在特定修饰。

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