Effective elution of antibodies by arginine and arginine derivatives in affinity column chromatography

被引:120
作者
Ejima, D [1 ]
Yumioka, R
Tsumoto, K
Arakawa, T
机构
[1] Ajinomoto Co Inc, Amino Sci Labs, Kawasaki, Kanagawa 2108681, Japan
[2] Univ Tokyo, Grad Sch Frontier Sci, Dept Med Genome Sci, Kashiwa, Chiba 2778562, Japan
[3] Alliance Prot Labs, Thousand Oaks, CA 91360 USA
关键词
arginine; protein A; affinity chromatography; eluate;
D O I
10.1016/j.ab.2005.07.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
It has been shown that the recovery of monomeric antibodies from protein A affinity chromatography is enhanced significantly by using arginine as an eluent. To extend the applications of arginine to antibody purification and obtain an insight into the mechanism of arginine elution, we compared arginine with citrate, guanidine hydrochloride (GdnHCl), arginine derivatives, and other amino acids in protein A chromatography. We also applied arginine to elution of polyclonal antibodies (pAbs) in antigen affinity chromatography. As described previously, arginine was effective in eluting monoclonal antibodies IgG1 and IgG4. Two arginine derivatives, acetyl-arginine and agmatine, resulted in efficient elution at pH 4.0 or higher, and this was comparable to arginine. On the other hand, other amino acids, such as glycine, proline, lysine, and histidine, are much less effective than arginine under identical pH conditions. Whereas elution increased with arginine concentration, elution with citrate was insignificant in excess of I M at pH 4.3. Arginine was also effective in fractionation of pAbs using antigen-conjugated affinity columns. Although GdnHCl was also effective under similar conditions, the eluted material showed more aggregation than did the protein eluted by arginine. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:250 / 257
页数:8
相关论文
共 24 条
[1]   Elution of antibodies from a Protein-A column by aqueous arginine solutions [J].
Arakawa, T ;
Philo, JS ;
Tsumoto, K ;
Yumioka, R ;
Ejima, D .
PROTEIN EXPRESSION AND PURIFICATION, 2004, 36 (02) :244-248
[2]   MECHANISM OF PROTEIN SALTING IN AND SALTING OUT BY DIVALENT-CATION SALTS - BALANCE BETWEEN HYDRATION AND SALT BINDING [J].
ARAKAWA, T ;
TIMASHEFF, SN .
BIOCHEMISTRY, 1984, 23 (25) :5912-5923
[3]   ALTERNATIVELY FOLDED STATES OF AN IMMUNOGLOBULIN [J].
BUCHNER, J ;
RENNER, M ;
LILIE, H ;
HINZ, HJ ;
JAENICKE, R ;
KIEFHABER, T ;
RUDOLPH, R .
BIOCHEMISTRY, 1991, 30 (28) :6922-6929
[4]   TEMPERATURE AND PH-DEPENDENCE OF IMMUNOGLOBULIN-G CONFORMATION [J].
CALMETTES, P ;
CSER, L ;
RAJNAVOLGYI, E .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1991, 291 (02) :277-283
[5]   PURIFICATION OF BACTERIALLY EXPRESSED SINGLE-CHAIN FV ANTIBODIES FOR CLINICAL-APPLICATIONS USING METAL CHELATE CHROMATOGRAPHY [J].
CASEY, JL ;
KEEP, PA ;
CHESTER, KA ;
ROBSON, L ;
HAWKINS, RE ;
BEGENT, RHJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 1995, 179 (01) :105-116
[6]   Fractionation of polyclonal antibodies to fragments of a neuroreceptor using three increasingly chaotropic solvents [J].
Caughey, DJ ;
Narhi, LO ;
Kita, Y ;
Meng, SY ;
Wen, DZ ;
Chen, W ;
Ratzkin, BJ ;
Fujimoto, J ;
Iwahara, T ;
Yamamoto, T ;
Arakawa, T .
JOURNAL OF CHROMATOGRAPHY B, 1999, 728 (01) :49-57
[7]   INSULIN-SEPHAROSE - IMMUNOREACTIVITY AND USE IN PURIFICATION OF ANTIBODY [J].
CUATRECASAS, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1969, 35 (04) :531-+
[8]  
Cuatrecasas P., 1971, METHOD ENZYMOL, V22, P345
[9]   IMMUNOAFFINITY CHROMATOGRAPHIC PURIFICATION OF RUSSELL VIPER VENOM FACTOR-X ACTIVATOR USING ELUTION IN HIGH-CONCENTRATIONS OF MAGNESIUM-CHLORIDE [J].
DURKEE, KH ;
ROH, BH ;
DOELLGAST, GJ .
PROTEIN EXPRESSION AND PURIFICATION, 1993, 4 (05) :405-411
[10]  
Ejima D, 1999, BIOTECHNOL BIOENG, V62, P301, DOI 10.1002/(SICI)1097-0290(19990205)62:3<301::AID-BIT6>3.3.CO