Antibody engineering toward high-sensitivity high-throughput immunosensing of small molecules

被引:53
作者
Kobayashi, Norihiro [1 ]
Oyama, Hiroyuki [1 ]
机构
[1] Kobe Pharmaceut Univ, Higashinada Ku, Kobe, Hyogo 6588558, Japan
关键词
SINGLE-CHAIN FV; SANDWICH ENZYME-IMMUNOASSAY; IMMUNE COMPLEX ASSAY; COLI MUTATOR CELLS; AFFINITY MATURATION; IN-VITRO; NONCOMPETITIVE IMMUNOASSAY; PHAGE DISPLAY; VARIABLE REGION; ANTIIDIOTYPE ANTIBODIES;
D O I
10.1039/c0an00603c
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Clinical and environmental analyses often require immunochemical detection and quantification of small molecules (haptens) that are available as biomarkers. However, the affinity ceilings of conventional anti-hapten antibodies, which are produced by immunizing animals, prevent subfemtomole-range determinations with competitive immunoassay formats. "Sandwich-type'' noncompetitive (immunometric) assays allow for sensitive determinations of macromolecules (subattomole-range) and the direct relationship between analyte amount and signal intensity provides higher accessibility to modern high-throughput sensing systems. Unfortunately, sandwich-type assays require that analytes have at least two epitopes, and thus are not applicable to haptens. Antibody engineering, i.e., genetic manipulation of antibody molecules, could provide artificially improved reagents that enable us to overcome these limitations. In this review, we summarize recent successful developments and applications of engineered antibodies for sensitive and high-throughput hapten sensing.
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页码:642 / 651
页数:10
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