DE NOVO DESIGN AND CONSTRUCTION OF AN INDUCIBLE GENE EXPRESSION SYSTEM IN MAMMALIAN CELLS

被引:18
作者
Kartsson, Maria [1 ,2 ,3 ]
Weber, Wilfried [1 ,2 ,3 ]
Fussenegger, Martin [3 ,4 ]
机构
[1] Univ Freiburg, Fac Biol, Freiburg, Germany
[2] Univ Freiburg, Ctr Biol Signaling Studies BIOSS, Freiburg, Germany
[3] Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, Basel, Switzerland
[4] Univ Basel, Fac Sci, Basel, Switzerland
来源
METHODS IN ENZYMOLOGY, VOL 497: SYNTHETIC BIOLOGY, METHODS FOR PART/DEVICE CHARACTERIZATION AND CHASSIS ENGINEERING, PT A | 2011年 / 497卷
关键词
ADJUSTABLE TRANSGENE EXPRESSION; TRANSCRIPTION CONTROL; REGULATED EXPRESSION; ESCHERICHIA-COLI; MICE; TETRACYCLINE; CIRCUIT; SWITCH; EUKARYOTES; VECTORS;
D O I
10.1016/B978-0-12-385075-1.00011-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Inducible expression systems represent the founding technology for the emergence of synthetic biology in mammalian cells. The core molecules in these systems are bacterial regulator proteins that bind to or dissociate from a cognate DNA operator sequence in response to an exogenous stimulus like a small-molecule inducer. In this chapter, we describe a generic protocol of how bacterial regulator proteins can be applied to the design, construction, and optimization of an inducible expression system in mammalian cells. By choosing regulator proteins with an appropriate small-molecule inducer, this protocol provides a straightforward approach for establishing biosensors, cell-to-cell communication systems, or tools to control gene expression in vivo.
引用
收藏
页码:239 / 253
页数:15
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