Protein engineering for self-assembling antibody molecules in an oriented manner

被引:4
|
作者
Aizawa, M [1 ]
Yun, K [1 ]
Haruyama, T [1 ]
Yanagida, Y [1 ]
Kobatake, E [1 ]
机构
[1] Tokyo Inst Technol, Fac Biosci & Biotechnol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
来源
SUPRAMOLECULAR SCIENCE | 1998年 / 5卷 / 5-6期
关键词
protein engineering; self-assembling; antibody; protein A; lipid-tagged antibody;
D O I
10.1016/S0968-5677(98)00120-5
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two types of protein engineering have been developed for self-assembling antibody (IgG) molecules in an oriented manner. The first is to tag a cysteine group to Protein A which has a specific affinity to the Fe part of IgG. The cysteine-tagged Protein A was self-assembled on the gold surface, which was followed by self-assembling: of IgG to Face the antigen recognition sites to the solution phase. The second is concerned with tailing a single chain antibody by lipid at the one terminal and the hexahistidinyl group at the other. The lipid and histidine-tailed single chain antibody was embedded in a liposome to make the antigen recognition site appear on the outsphere, which was immobilized on the Ni-treated mica surface through chelating of the histidine tail. The individual liposome was clearly imaged by a tapping mode of AFM. (C) 1998 Elsevier Science Limited. All rights reserved.
引用
收藏
页码:761 / 764
页数:4
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