Bjellqvist B, Linderholm M, Ostergren K, Strahler J
Pharmacia-LKB Biotechnology AB, Bromma, Sweden.
Electrophoresis. 1988 Sep;9(9):453-63. doi: 10.1002/elps.1150090903.
The relations describing the concentration changes at moving boundaries in a medium containing bound, buffering group are derived for a system which, except for hydrogen and hydroxyl ions, contains one anionic and one cationic mobile constituent. The relations found have been used to calculate concentrations and conductivities in zones developing in immobilized pH gradients. Assumptions used in the calculations as well as conductivity ratios between zones have been experimentally controlled and were found to reasonably agree with expectations. It is also shown how difference in transference numbers between sample droplet and gel will cause concentration and pH changes at the gel-sample droplet interfaces and it is explained how these changes are related to ionic concentrations in the gel. The high concentration zone generated at one of the interfaces will be transported into the gel. This transport has been numerically simulated and experimentally verified. The low concentration generated at the opposite interface will cause titration impeding sample entrance in the gel through this interface even when the gel contains ions other than H+ or OH- transported towards the interface. The described phenomena explain the dependence of lateral spreading, precipitation at the application site as well as streaking and smearing along sample lanes, on the type and concentration of low molecular weight ions originally present in the gel.
对于一个除了氢离子和氢氧根离子外还包含一种阴离子和一种阳离子移动成分的体系,推导了描述含有结合缓冲基团的介质中移动边界处浓度变化的关系式。所得到的关系式已用于计算固定pH梯度中形成区域的浓度和电导率。计算中使用的假设以及区域之间的电导率比已通过实验控制,并且发现与预期合理相符。还展示了样品液滴和凝胶之间迁移数的差异如何导致凝胶 - 样品液滴界面处的浓度和pH变化,并解释了这些变化与凝胶中离子浓度的关系。在其中一个界面处产生的高浓度区域将被传输到凝胶中。这种传输已通过数值模拟和实验验证。在相对界面处产生的低浓度将导致滴定阻碍样品通过该界面进入凝胶,即使凝胶中含有除了向该界面传输的H⁺或OH⁻之外的离子。所描述的现象解释了横向扩散、施加部位的沉淀以及沿样品泳道的条纹和拖尾现象对凝胶中最初存在的低分子量离子类型和浓度的依赖性。