Godin D V, Garnett M
J Membr Biol. 1976 Aug 26;28(2-3):143-68. doi: 10.1007/BF01869694.
The perturbational effects of monovalent and divalent cations on human erythrocyte membranes were analyzed by examining their influence on kinetic and structural characteristics of trinitrobenzenesulfonic acid (TNBS) incorporation into the amino groups of protein and phospholipid structural components. The stimulatory effects of monovalent cations on TNBS incorporation, which were size-independent and attributed to nonspecific membrane alterations resulting from ionic strength factors, contrasted with the more pronounced stimulatory properties of divalent cations which were markedly size-dependent. These stimulatory effects of cations on TNBS incorporation were associated with alterations not only in rate but also in activation energy in incorporation. Changes in activation energy produced by divalent cations paralleled their ability to perturb membrane protein components and probably reflected changes in probe permeation. The rate of TNBS incorporation exhibited a dependence on divalent cation ionic radius which paralleled ion-induced perturbations in the labelling of the membrane amino phospholipid phosphatidylethanolamine. Divalent cations differed both in the relative extent and in the characteristics of protein and phospholipid perturbation. Alkaline earth cations behaved as a rather homogeneous group while Ni++, Co++ and Mn++ constituted a second heterogeneous group. The influence of monovalent and divalent cations on the hemolytic behavior of intact erythrocytes paralleled their effects on TNBS incorporation into isolated membranes rather closely. It is suggested that TNBS incorporation may provide a valuable means of analyzing functionally relevant cation-induced alterations in biological membranes in general.
通过研究一价和二价阳离子对三硝基苯磺酸(TNBS)掺入蛋白质和磷脂结构成分氨基的动力学和结构特征的影响,分析了它们对人红细胞膜的扰动作用。一价阳离子对TNBS掺入的刺激作用与离子强度因素导致的非特异性膜改变有关,与离子大小无关,而二价阳离子的刺激特性更明显,且明显与离子大小有关。阳离子对TNBS掺入的这些刺激作用不仅与掺入速率的改变有关,还与掺入的活化能的改变有关。二价阳离子引起的活化能变化与其扰动膜蛋白成分的能力平行,可能反映了探针渗透的变化。TNBS掺入速率表现出对二价阳离子离子半径的依赖性,这与离子诱导的膜氨基磷脂磷脂酰乙醇胺标记扰动平行。二价阳离子在蛋白质和磷脂扰动的相对程度和特征方面都有所不同。碱土金属阳离子表现为一个相当均匀的组,而Ni++、Co++和Mn++构成了另一个异质组。一价和二价阳离子对完整红细胞溶血行为的影响与其对TNBS掺入分离膜的影响相当密切地平行。有人认为,一般来说,TNBS掺入可能为分析生物膜中功能相关的阳离子诱导变化提供一种有价值的手段。