Freise J, Magerstedt P, Schmidt E
J Clin Chem Clin Biochem. 1976 Dec;14(12):589-94.
Using the sera from 20 patients with elevated gamma-glutamyl transferase activity (EC 2.3.2.2) due to intra- or posthepatic cholestasis, the enzyme was separated into four bands by cellulose acetate foil electrophoresis. The gamma-glutamyl transferase pattern permitted no differentiation between intra- or posthepatic cholestasis. Protein and lipid electrophoresis was performed simultaneously for each serum. It was found that a gamma-glutamyl transferase band, which appeared at the origin in 11 sera, was only observed in lipaemic sera containing chylomicrons. This band of gamma-glutamyl transferase does not, however, represent a true isoenzyme, because it results from a complex between chylomicrons and gamma-glutamyl transferase, which is separated with the chylomicrons, or is produced by the mixing of sera.
使用20例因肝内或肝后胆汁淤积导致γ-谷氨酰转移酶活性(EC 2.3.2.2)升高的患者的血清,通过醋酸纤维素薄膜电泳将该酶分离成四条带。γ-谷氨酰转移酶图谱无法区分肝内胆汁淤积和肝后胆汁淤积。同时对每份血清进行蛋白质和脂质电泳。结果发现,在11份血清中出现在原点处的一条γ-谷氨酰转移酶带,仅在含有乳糜微粒的脂血血清中观察到。然而,这条γ-谷氨酰转移酶带并不代表真正的同工酶,因为它是由乳糜微粒与γ-谷氨酰转移酶之间的复合物产生的,该复合物与乳糜微粒一起分离,或者是由血清混合产生的。