Guasch R M, Guerri C, O'Connor J E
Departamento de Bioquímica (Centro de Referencia Izasa-Coulter), Facultad de Medicina, Universidad de Valencia, Spain.
Exp Cell Res. 1993 Jul;207(1):136-41. doi: 10.1006/excr.1993.1172.
Flow cytometry (FCM) has been used repeatedly to study lectin binding to whole cells. However, there are very few attempts to analyze glycoconjugates in isolated subcellular organelles. We have applied FCM to quantitate the specific binding of fluorescein-conjugated concanavalin A (FITC-Con A) to isolated cis and trans fractions of rat liver Golgi complex, the cell compartment involved in glycoprotein maturation and sorting. Our results show similar intensities of Con A-specific binding in the two fractions. Using this method we show a decreased FITC-Con A binding to both Golgi fractions in ethanol-treated rats, which is consistent to previous work on alcoholic effects on galactosyltransferase. The possible applications of this technique are discussed.
流式细胞术(FCM)已被反复用于研究凝集素与全细胞的结合。然而,很少有人尝试分析分离的亚细胞器中的糖缀合物。我们应用FCM来定量荧光素偶联的伴刀豆球蛋白A(FITC-Con A)与大鼠肝脏高尔基体复合体分离的顺式和反式部分的特异性结合,高尔基体复合体是参与糖蛋白成熟和分选的细胞区室。我们的结果显示,两个部分中Con A特异性结合的强度相似。使用这种方法,我们发现乙醇处理的大鼠中,FITC-Con A与两个高尔基体部分的结合均减少,这与先前关于酒精对半乳糖基转移酶影响的研究结果一致。本文讨论了该技术的可能应用。