Two Elution Mechanisms of MEP Chromatography

被引:2
作者
Arakawa, Tsutomu [1 ]
Tokunaga, Masao [2 ]
Maruyama, Takuya [3 ]
Shiraki, Kentaro [3 ]
机构
[1] Alliance Prot Labs, 6042 Cornerstone Court West, San Diego, CA 92121 USA
[2] Kagoshima Univ, Fac Agr, Appl & Mol Microbiol, 1-21-24 Korimoto, Kagoshima 8900065, Japan
[3] Univ Tsukuba, Fac Pure & Appl Sci, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058573, Japan
关键词
MEP HyperCel; chromatography; antibody; arginine; elution; acidic pH; CHARGE INDUCTION CHROMATOGRAPHY; HYDROPHOBIC INTERACTION CHROMATOGRAPHY; PROTEIN-A; MOLECULAR-MECHANISM; AMINO-ACIDS; ARGININE; ANTIBODY; PURIFICATION; AFFINITY; COLUMN;
D O I
10.2174/1389203718666171117105132
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MEP (mercapto-ethyl-pyridine) HyperCel is one of the hydrophobic charge induction chromatography (HCIC) resins. Under normal operation, proteins are bound to the MEP resin at neutral pH, at which MEP is not charged, mostly via hydrophobic interaction. MEP has a pyridine group, whose pK is 4.8, and hence is positively charged at acidic pH range. Based on the binding mechanism (i.e., hydrophobic interaction) and the induced positive charge at acidic pH, there may be two ways to elute the bound proteins. One way is to bring the pH down to protonate both MEP resin and the bound protein, leading to charge repulsion and thereby elution. Another way is to use hydrophobic interaction modifiers, which are often used in hydrophobic interaction chromatography, to reduce hydrophobic interaction. Here, we summarize such two possible elution approaches.
引用
收藏
页码:28 / 33
页数:6
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