American Journal of Hematology · 1978 · 42 citations · 25 references
Life SciencesBiochemistryAnalytical ChemistryBioseparationsProtein BiochemistryHemoglobin PhysiologyProtein ElectrophoresisProtein PurificationProtein SeparationHemoglobin LevelsHemoglobin StructureIsoelectric FocusingIsoelectric PointPh DependencePh Effects On SeparationProtein FocusingProtein Separation Techniques
A modified type of isolectric focusing has been applied successfully to the separation of hemoglobin A1C (HbA1C) from HbA in normal and diabetic cell lysates. It consists of transforming a linear pH gradient into a nonlinear one, by the addition of an amphoteric substance ("separator" or "pH gradient modifier") with an isoelectric point (pI) close to the pI's of the two hemoglobins. Among the "modifiers" tested, histidine, proline, threonine, beta-alanine, 6-amino caproic acid, and 5-amino valeric acid are not useful in the hemoglobin pI range (pH 6.9--7.0). The dipeptide histidyl-glycine (pI = 6.8; pI-pK1 = 1) is very efficient in flattening the pH gradient, in the hemoglobin region. even when added in low concentrations (10--100 mM), thus affording full resolution of the two hemoglobin species.
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David L. Drabkin · Journal of Biological Chemistry · 1946 · 921 citations · Full text
In vitro synthesis of hemoglobin A<sub>Ic</sub>
Rudolf Flückiger, Kaspar H. Winterhalter · FEBS Letters · 1976 · 460 citations · Full text