Van Noorden C J, Jonges G N
Academic Medical Centre, University of Amsterdam, Laboratory of Cell Biology and Histology, The Netherlands.
Histochem J. 1995 Feb;27(2):101-18. doi: 10.1007/BF00243905.
Estimations of metabolic rates in cells and tissues and their regulation on the basis of kinetic properties of enzymes in diluted solutions may not be applicable to intact living cells or tissues. Enzymes often behave differently in living cells because of the high cellular protein content that can lead to homologous and heterologous associations of protein molecules. These associations often change the kinetics of enzymes as part of post-translational regulation mechanisms. An overview is given of these interactions between enzyme molecules or between enzyme molecules and structural elements in the cell, such as the cytoskeleton. Biochemical and histochemical methods are discussed that have been developed for in vivo and in situ analyses of enzyme reactions, particularly for the study of effects of molecular interactions. Quantitative (histochemical) analysis of local enzyme reactions or fluxes of metabolites has become increasingly important. At present, it is possible to calculate local concentrations of substrates in cells or tissue compartments and to express local kinetic parameters in units that are directly comparable with those obtained by biochemical assays of enzymes in suspensions. In situ analysis of the activities of a number of enzymes have revealed variations in their kinetic properties (Km and Vmax) in different tissue compartments. This stresses the importance of in vivo or in situ analyses of cellular metabolism. Finally, histochemical determinations of enzyme activity in parallel with immunohistochemistry for the detection of the total number of enzyme molecules and in situ hybridization of its messenger RNA allow the analysis of regulation mechanisms at all levels between transcription of the gene and post-translational activity modulation.
基于稀释溶液中酶的动力学特性对细胞和组织代谢率及其调节的估计可能不适用于完整的活细胞或组织。由于细胞内蛋白质含量高,酶在活细胞中的行为往往不同,这可能导致蛋白质分子的同源和异源缔合。作为翻译后调节机制的一部分,这些缔合常常会改变酶的动力学。本文综述了酶分子之间或酶分子与细胞内结构元件(如细胞骨架)之间的这些相互作用。讨论了为酶反应的体内和原位分析而开发的生化和组织化学方法,特别是用于研究分子相互作用的影响。局部酶反应或代谢物通量的定量(组织化学)分析变得越来越重要。目前,可以计算细胞或组织区室中底物的局部浓度,并以与通过悬浮液中酶的生化测定获得的单位直接可比的单位来表示局部动力学参数。对多种酶活性的原位分析揭示了它们在不同组织区室中的动力学特性(Km和Vmax)存在差异。这强调了细胞代谢的体内或原位分析的重要性。最后,酶活性的组织化学测定与用于检测酶分子总数的免疫组织化学以及其信使RNA的原位杂交相结合,可以分析基因转录和翻译后活性调节之间所有水平的调节机制。