Kraml J, Lojda Z
Acta Univ Carol Med Monogr. 1977(77 Pt 1):83-94.
Membrane-bound enzymes have certain specific differences compared with soluble enzymes. Membrane-binding often enables greater catalytic activity of associated enzymatic reactions, their regulation by low molecular weight substances (substrates and allosteric effectors, hormones) and compartmentation, etc. On the other hand, the binding of enzymes to membranes causes considerable difficulties as regards their isolation and the determination of their homogeneity and substrate specificity. Membrane enzymes provide a unique opportunity for studying the biogenesis of membranes and their physiological properties, however. These problems are discussed in relation to two types of membranes--the inner mitochondrial membrane and the membrane of the brush border of the small intestine. An example of the utilization of immunochemical methods is given in the results of a study of biosynthesis of the cytochrome oxidase complex in yeast cells. In the case of the brush border of the mammalian small intestine, the fact that certain enzymes, which are also of clinical significance from the aspect of congenital genetic defects, can be isolated only as complexes, constitutes a very real problem. This applies particularly to the sucrase-isomaltase complex and the lactase-beta-glucosidase complex. Solving questions of substrate specificity is of significance for the choice of a suitable analytical or histochemical method. The common regulation of these complexes gives an insight into the problems of membrane biogenesis, however. Immunochemical methods can be employed as sensitive criteria to support biochemical and morphological studies. Collaboration between the biochemist and histochemist proved especially valuable when determining the substrate specificity of enzymes (glycosidases) in relation to histochemical substrates, when applying histochemical methods for detecting enzymatic activity in immunoprecipitates and acrylamide gels and in immunohistochemical studies of the localization and developmental differentiation of the enzymes of the brush border of the small intestine.
与可溶性酶相比,膜结合酶具有某些特定的差异。膜结合通常能使相关酶促反应具有更高的催化活性,使其受到低分子量物质(底物、变构效应物、激素)的调节以及实现区室化等。另一方面,酶与膜的结合在其分离以及均一性和底物特异性的测定方面造成了相当大的困难。然而,膜酶为研究膜的生物发生及其生理特性提供了独特的机会。这些问题将结合两种类型的膜——线粒体内膜和小肠刷状缘膜进行讨论。在酵母细胞细胞色素氧化酶复合物生物合成的研究结果中给出了免疫化学方法应用的一个例子。就哺乳动物小肠刷状缘而言,某些从先天性遗传缺陷角度来看也具有临床意义的酶只能作为复合物分离出来,这一事实构成了一个非常现实的问题。这尤其适用于蔗糖酶 - 异麦芽糖酶复合物和乳糖酶 - β - 葡萄糖苷酶复合物。解决底物特异性问题对于选择合适的分析或组织化学方法具有重要意义。然而,这些复合物的共同调节有助于深入了解膜生物发生的问题。免疫化学方法可作为敏感标准来支持生化和形态学研究。当确定酶(糖苷酶)相对于组织化学底物的底物特异性、将组织化学方法应用于检测免疫沉淀物和丙烯酰胺凝胶中的酶活性以及在小肠刷状缘酶的定位和发育分化的免疫组织化学研究中时,生物化学家和组织化学家之间的合作被证明特别有价值。