Anti body-induced oligomerization and activation of an engineered reporter enzyme

被引:11
|
作者
Geddie, Melissa L. [1 ]
Matsumura, Ichiro [1 ]
机构
[1] Emory Univ, Sch Med, Rollins Res Ctr, Dept Biochem,Ctr Fundamental & Appl Mol Evolut, Atlanta, GA 30322 USA
关键词
biosensor; molecular switch; high-throughput screen; induced dimerization; reporter enzyme;
D O I
10.1016/j.jmb.2007.03.076
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
Our objective is to produce a protein biosensor (or molecular switch) that is specifically activated in solution by a monoclonal antibody. Many effector-dependent enzymes have evolved in nature, but the introduction of a novel regulatory mechanism into a normally unregulated enzyme poses a difficult design problem. We used site-saturation mutagenesis and screening to generate effector-activated variants of the reporter enzyme beta-glucuronidase (GUS). The specific activity of the purified epitope-tagged GUS variant was increased by up to similar to 500-fold by the addition of an equimolar concentration of a monoclonal antibody. This molecular switch is modular in design, so it can easily be re-engineered for the detection of other peptide-specific antibodies. Such antibody-activated reporters could someday enable point-of-care serological assays for the rapid detection of infectious diseases. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1052 / 1059
页数:8
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