Deleers M
Res Commun Chem Pathol Pharmacol. 1985 Aug;49(2):277-94.
Binding of cations to membranes may be the basis for explaining some of the effects of several neurotoxic cations. The binding of Al3+ and the displacement of Ca2+ by Al3+ is studied with the aid of a simple mathematical approach described here and giving the same results when compared to the mathematical formalism described by Nir and Bentz. The method allows the simulation of membranes with low surface charge densities that are relevant for biochemical and pathological implications. Fluorescence quenching of the phospholipid analogue 1-palmitoyl-2-nitrobenzoxadiazol amino caproyl- phosphatidyl choline (C6-NBD-Ptd Cho) embedded in phosphatidyl serine membranes is used to determine the competition between calcium and aluminum for binding. The effect of aluminum in the presence of chelating agents is also studied by quenching experiments. Finally, inhibition of 45Ca2+ binding to phosphatidyl serine has also been investigated in a two-phase system.
阳离子与膜的结合可能是解释几种神经毒性阳离子某些作用的基础。借助本文所述的一种简单数学方法研究了Al3+的结合以及Al3+对Ca2+的置换,与Nir和Bentz描述的数学形式主义相比,该方法给出了相同的结果。该方法允许模拟具有低表面电荷密度的膜,这与生化和病理学意义相关。嵌入磷脂酰丝氨酸膜中的磷脂类似物1-棕榈酰-2-硝基苯并恶二唑氨基己酰-磷脂酰胆碱(C6-NBD-Ptd Cho)的荧光猝灭用于确定钙和铝在结合上的竞争。还通过猝灭实验研究了螯合剂存在下铝的作用。最后,在两相系统中也研究了45Ca2+与磷脂酰丝氨酸结合的抑制作用。