The intracellular antibody capture technology (IACT): Towards a consensus sequence for intracellular antibodies

被引:107
作者
Visintin, M
Settanni, G
Maritan, A
Graziosi, S
Marks, JD
Cattaneo, A [1 ]
机构
[1] Scuola Int Super Studi Avanzati, SISSA, I-34013 Trieste, Italy
[2] INFM Unit, I-34013 Trieste, Italy
[3] Lay Line Genom SPA, I-34100 Trieste, Italy
[4] Univ Calif San Francisco, Dept Anesthesia & Pharmaceut Chem, San Francisco, CA 94110 USA
关键词
intrabodies; single-chain Fv; functional genomics; TAU; Alzheimer's disease;
D O I
10.1006/jmbi.2002.5392
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
We describe the application of an intracellular antibody capture technology (IACT) as a generic in vivo selection procedure for isolating intracellular antibodies or ICAbs. IACT was applied to the de novo selection of functional ICAbs against the microtubule-associated protein TAU, found in neurofibrillary lesions of Alzheimer's disease brains. A panel of 17 different ICAbs was created which bind TAU inside cells and the epitopes recognized by the selected ICAbs have been determined by an in vivo epitope mapping procedure. Finally, sequence analysis showed that the IACT-derived ICAbs are characterized by a common signature of conserved amino acid residues, suggesting that the IACT naturally selects a sort of "captured consensus sequence" for intracellular antibodies. The development of IACT, together with the possibility of scaling up in a high throughput and automated format, makes IACT a new enabling tool for target validation in functional genomics and global proteomics. (C) 2002 Elsevier Science Ltd.
引用
收藏
页码:73 / 83
页数:11
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