Generation of antibodies against membrane proteins

被引:16
作者
Hamakubo, Takao [1 ]
Kusano-Arai, Osamu [1 ,2 ]
Iwanari, Hiroko [1 ]
机构
[1] Univ Tokyo, Res Ctr Adv Sci & Technol, Dept Quantitat Biol & Med, Meguro Ku, Tokyo 1538904, Japan
[2] Inst Immunol Co Ltd, Bunkyo Ku, Tokyo 1120004, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2014年 / 1844卷 / 11期
基金
日本学术振兴会;
关键词
Monoclonal antibody; Baculovirus; Membrane protein; NUCLEAR POLYHEDROSIS-VIRUS; MONOCLONAL-ANTIBODIES; COUPLED RECEPTOR; BUDDED BACULOVIRUS; T-CELLS; FUNCTIONAL RECONSTITUTION; TUMOR MICROENVIRONMENT; BISPECIFIC ANTIBODIES; CANCER-IMMUNOTHERAPY; IMMUNE-RESPONSES;
D O I
10.1016/j.bbapap.2014.08.007
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
The monoclonal antibody has become an important therapeutic in the treatment of both hematological malignancies and solid tumors. The recent success of antibody-drug conjugates (ADCs) has broadened the extent of the potential target molecules in cancer immunotherapy. As a result, even molecules of low abundance have become targets for cytotoxic reagents. The multi-pass membrane proteins are an emerging target for the next generation antibody therapeutics. One outstanding challenge is the difficulty in preparing a sufficient amount of these membrane proteins so as to be able to generate the functional antibody. We have pursued the expression of various membrane proteins on the baculovirus particle and the utilization of displayed protein for immunization. The strong antigenicity of the virus acts either as a friend or foe in the making of an efficient antibody against an immunologically tolerant antigen. This article is part of a Special Issue entitled: Recent advances in molecular engineering of antibody. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:1920 / 1924
页数:5
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