Chang J, Guo L
Department of Chemistry, Northwest University, Xi'an, 710069.
Se Pu. 1997 Mar;15(2):141-3.
An abrupt change of the eluting curve of proteins in the RPC and HIC was reported in the previous paper. Here, we present a new multi-injection method of proteins in which the sample may be injected for many times in the same chromatographic run. When the composition of mobile phase is far away from the position of the abrupt change, the multi-injection of proteins before and/or after starting a gradient elution for one chromatographic separation in the RPC and HIC can be performed. Thus we may obtain the same chromatogram and retention of proteins as the ordinary one. This method can be used to overcome the difficulty that the loop is too small for injection big volume of sample solution. A larger sample size can be injected by many times in one chromatographic run to save time and to decrease the consumption of the experimental material. If there exist some impure proteins of weak retention, the impure proteins may go through the column with the solution A when the selected concentration of mobile phase is suitable. Therefore, a fixed column size can adsorb more related proteins, that is the effective column capacity is relatively raised. This injection method has an important value in the preparative chromatography of proteins.
上一篇论文报道了反相色谱(RPC)和疏水作用色谱(HIC)中蛋白质洗脱曲线的突然变化。在此,我们提出一种新的蛋白质多次进样方法,即在同一色谱运行中样品可多次进样。当流动相组成远离突然变化的位置时,在RPC和HIC的一次色谱分离中,在梯度洗脱开始之前和/或之后均可进行蛋白质的多次进样。因此,我们可以获得与常规色谱图相同的色谱图和蛋白质保留情况。该方法可用于克服定量环过小而无法进样大量样品溶液的困难。在一次色谱运行中通过多次进样可以注入更大体积的样品,从而节省时间并减少实验材料的消耗。如果存在一些保留较弱的不纯蛋白质,当所选流动相浓度适当时,这些不纯蛋白质可能会随溶液A一起通过色谱柱。因此,固定尺寸的色谱柱可以吸附更多相关蛋白质,即有效柱容量相对提高。这种进样方法在蛋白质制备色谱中具有重要价值。