Reduced immunogenicity of β-lactoglobulin by conjugating with chitosan

被引:58
作者
Aoki, Tomomi [1 ]
Iskandar, Silvia [1 ]
Yoshida, Tadashi [1 ]
Takahashi, Koji [1 ]
Hattori, Makoto [1 ]
机构
[1] Tokyo Univ Agr & Technol, Div Agrisci & Biosci, Inst Symbiot Sci & Technol, Tokyo 1838509, Japan
关键词
beta-lactoglobulin; chitosan; protein conjugation; functional improvement; reduced immunogenicity;
D O I
10.1271/bbb.50398
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Bovine beta-lactoglobulin (beta-LG) was conjugated with chitosan (CHS) by means of a water-soluble carbodiimide to reduce the inummogenicity of beta-LG. Each beta-LG-CHS conjugate was purified by ion-exchange chromatography and hydrophobic chromatography. The conjugation between beta-LG and CHS was confirmed by SDS-PAGE, the isoelectric point of the conjugate being higher than that of beta-LG. Two types of the beta-LG-CHS conjugate were obtained with molar ratios of beta-LG to CHS of 1:1 (F1) and 1:2 (F2). Structural analyses by fluorescence measurement, ELISA with monoclonal antibodies and retinol-binding activity indicated that the conjugates had almost maintained the native structure of beta-LG. The antigenicity of the beta-LG-CHS conjugates was similar to that of beta-LG in C3H/He mice. Reduction of the immunogemicity of beta-LG was achieved by conjugation with CHS. In particular, F2 showed very low immunogenicity. B cell epitopes of beta-LG and the conjugates recognized in C3H/He mice were determined with 15-mer multi-pin peptide; the linear epitope profiles of the conjugates were found to be similar to those of beta-LG, while the antibody response to each epitope was dramatically reduced. Conjugation of beta-LG with chitosan was effective for reducing the immunogenicity of beta-LG.
引用
收藏
页码:2349 / 2356
页数:8
相关论文
共 34 条
[1]
ON FRACTIONATION OF BETA-LACTOGLOBULIN AND ALPHA-LACTALBUMIN [J].
ARMSTRONG, JM ;
MCKENZIE, HA ;
SAWYER, WH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1967, 147 (01) :60-+
[2]
A MAJOR CONTINUOUS ALLERGENIC EPITOPE OF BOVINE BETA-LACTOGLOBULIN RECOGNIZED BY HUMAN IGE BINDING [J].
BALL, G ;
SHELTON, MJ ;
WALSH, BJ ;
HILL, DJ ;
HOSKING, CS ;
HOWDEN, MEH .
CLINICAL AND EXPERIMENTAL ALLERGY, 1994, 24 (08) :758-764
[3]
BINDING AFFINITIES OF RETINOL AND RELATED COMPOUNDS TO RETINOL BINDING-PROTEINS [J].
COGAN, U ;
KOPELMAN, M ;
MOKADY, S ;
SHINITZKY, M .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1976, 65 (01) :71-78
[5]
DISCHE Z, 1950, J BIOL CHEM, V184, P517
[6]
FUTTERMAN S, 1972, J BIOL CHEM, V247, P5168
[7]
T-CELL DETERMINANT STRUCTURE - CORES AND DETERMINANT ENVELOPES IN 3 MOUSE MAJOR HISTOCOMPATIBILITY COMPLEX HAPLOTYPES [J].
GAMMON, G ;
GEYSEN, HM ;
APPLE, RJ ;
PICKETT, E ;
PALMER, M ;
AMETANI, A ;
SERCARZ, EE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (03) :609-617
[8]
Hattori M, 2000, J AGR FOOD CHEM, V48, P3789, DOI 10.1021/jf000204z
[9]
Reduced immunogenicity of β-lactoglobulin by conjugation with carboxymethyl dextran [J].
Hattori, M ;
Nagasawa, K ;
Ohgata, K ;
Sone, N ;
Fukuda, A ;
Matsuda, H ;
Takahashi, K .
BIOCONJUGATE CHEMISTRY, 2000, 11 (01) :84-93
[10]
HATTORI M, 1993, J BIOL CHEM, V268, P22414