化学
膜
分子
膜蛋白
色谱法
生物物理学
蛋白质A
高分辨率
分辨率(逻辑)
分子质量
分子识别
抗体
分子动力学
小分子
分子探针
靶蛋白
生物化学
过程(计算)
分子模型
作者
Tingting Wan,Huiying Wang,Xueting You,Kesheng Ben,Yifeng Li
出处
期刊:Membranes
[Multidisciplinary Digital Publishing Institute]
日期:2026-11-09
卷期号:16 (11): 381-381
标识
DOI:10.3390/membranes16110381
摘要
We previously demonstrated that Sartobind Rapid A Protein A membrane provides better resolution than traditional resin-based Protein A column. It seems that, in comparison to the Protein A column, Sartobind Rapid A membrane can better differentiate species with different molecular weights. In the current work, we further studied Sartobind Rapid A’s molecular weight-based separation potential by using it to process eight Fc-containing molecules with distinct molecular weights. The data suggested that, except for one molecule, there is a strong correlation between a molecule’s retention time and its molecular weight. In general, larger molecules tend to have longer retention. In relevance to its application in antibody purification, Sartobind Rapid A membrane’s molecular weight-based separation potential can be translated into strong byproduct-removing capabilities. As demonstrated in the present work, under optimized conditions, Sartobind Rapid A membrane effectively removed aggregates and half-antibody, two common byproducts that are remarkably different from the product in molecular weight. Thus, Sartobind Rapid A membrane’s unique separation capability makes it a more attractive tool than resin-based Protein A columns in antibody/Fc-fusion purification, especially for molecules with complex byproduct profiles.
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