Righetti P G, Brown R P, Stone A L
Biochim Biophys Acta. 1978 Aug 17;542(2):232-44. doi: 10.1016/0304-4165(78)90019-3.
The mechanism of complexation of pI range 3.5--5 Ampholine to heparin in isoelectric focusing has been explored by the dye-binding technique at different pH values in solution. There is no significant interaction between heparin and Ampholine at pH 6.7. Weak, or selective, binding occurs at pH 5.1, and very strong interaction at pH 3.5. In the latter system, the Ampholine components appear to behave as polycations due to their ordered sequence of positive charges, each two methylene groups apart, which favors a strong binding to polyanions. In addition, there appear to be variable stoichiometries for the strong binding between heparin and Ampholine, depending on their relative amounts. It is proposed that at a low ratio of heparin to Ampholine (Ampholine excess), aggregation is perpendicular to the heparin chain, with the end ammonium charge of each Ampholine molecule neutralizing one negative charge along the heparin molecule; at higher ratios (heparin excess), the bound Ampholine segment is aligned parallel to the heparin molecule, so that on the average one Ampholine component neutralizes approx. three negative charges. The banding of heparin in isoelectric focusing in the pH range 3.0--4.5 can be explained by aggregation of the various components on heparin in amounts dependent upon the net charge on the Ampholine species at the given pH, and upon the changing stoichiometries as a function of the variation in ratio of heparin to Ampholine along the pH gradient. Binding of Ampholine to polygalacturonate was also demonstrated in excess Ampholine in a pH range dependent on the degree of protonation of the carboxyl groups of this acidic polysaccharide as well as on the net positive charge of the Ampholine. The aggregation seen at pH 4.2--4.5 led to the prediction and subsequent demonstration that polygalacturonate would also exhibit binding upon isoelectric focusing. This supports the hypothesis that aggregation of Ampholine on polyanions having sufficient charge density is a general phenomenon which can lead to spurious banding of certain polymers at appropriate pH ranges in isoelectric focusing. On the basis of their behavior in isoelectric focusing at pH 3.0--4.5, strength of aggregation of the polyanions studied appears to be heparin A = heparin B greather than polyglutamate greater than carboxyl-reduced heparin B greater than polygalacturonic acid.
通过染料结合技术,在溶液中不同pH值条件下,研究了等电聚焦中pI范围为3.5 - 5的两性电解质与肝素的络合机制。在pH 6.7时,肝素与两性电解质之间无显著相互作用。在pH 5.1时发生弱的或选择性的结合,而在pH 3.5时存在非常强的相互作用。在后者体系中,两性电解质组分由于其带正电荷的有序序列(每隔两个亚甲基带一个正电荷)而表现为聚阳离子,这有利于与聚阴离子形成强结合。此外,肝素与两性电解质之间强结合的化学计量比似乎可变,这取决于它们的相对量。有人提出,在肝素与两性电解质比例较低时(两性电解质过量),聚集垂直于肝素链,每个两性电解质分子的末端铵电荷中和肝素分子上的一个负电荷;在较高比例时(肝素过量),结合的两性电解质片段与肝素分子平行排列,因此平均一个两性电解质组分中和约三个负电荷。在pH 3.0 - 4.5的等电聚焦中肝素的条带现象可以解释为,各种组分在肝素上的聚集量取决于给定pH下两性电解质种类的净电荷,以及随着肝素与两性电解质比例沿pH梯度变化而改变的化学计量比。在过量两性电解质存在下,在取决于这种酸性多糖羧基质子化程度以及两性电解质净正电荷的pH范围内,也证明了两性电解质与聚半乳糖醛酸的结合。在pH 4.2 - 4.5时观察到的聚集导致了这样的预测及随后的证明,即聚半乳糖醛酸在等电聚焦时也会表现出结合。这支持了这样的假设,即两性电解质在具有足够电荷密度的聚阴离子上的聚集是一种普遍现象,它可导致某些聚合物在等电聚焦的适当pH范围内出现假条带现象。根据它们在pH 3.0 - 4.5等电聚焦中的行为,所研究的聚阴离子的聚集强度似乎为:肝素A = 肝素B>聚谷氨酸>羧基还原的肝素B>聚半乳糖醛酸。