Fulton S, Meys M, Protentis J, Afeyan N B, Carlton J, Haycock J
PerSeptive Biosystems, Cambridge, MA 02139.
Biotechniques. 1992 May;12(5):742-7.
Cation exchange was compared to reversed-phase chromatography for the preparative purification of a 28-residue peptide (vasoactive intestinal polypeptide) on the 100-mg scale. Optimized high-speed, high-resolution methods were developed for both chromatographic modes on POROS Perfusion Chromatography flow-through particle chromatography columns. While both methods appeared to provide similar purity, the cation exchange column had approximately ten times the loading capacity per unit column volume as the reversed-phase column. Five-minute methods for desalting the cation exchange-purified peptide and analysis of fractions were developed using small reversed-phase columns. The cation-exchange method was scaled up to process 95 mg of crude peptide in a 12-min run.
在100毫克规模上,将阳离子交换与反相色谱法用于一种28个残基的肽(血管活性肠肽)的制备性纯化进行比较。在POROS灌注色谱流通颗粒色谱柱上,针对两种色谱模式开发了优化的高速、高分辨率方法。虽然两种方法似乎都能提供相似的纯度,但阳离子交换柱每单位柱体积的负载量约为反相柱的十倍。使用小型反相柱开发了用于阳离子交换纯化肽脱盐和馏分分析的5分钟方法。阳离子交换法放大后,在12分钟的运行中可处理95毫克粗肽。