Small-Molecule Regulators for Gene Switches to Program Mammalian Cell Behaviour

被引:4
作者
Mansouri, Maysam [1 ]
Fussenegger, Martin [1 ,2 ]
机构
[1] Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, Klingelbergstr 48, CH-4056 Basel, Switzerland
[2] Univ Basel, Fac Sci, Klingelbergstr 48, CH-4056 Basel, Switzerland
基金
欧洲研究理事会;
关键词
Small molecules; Synthetic biology; Mammalian cell engineering; Cell therapy; Gene therapy; SYNTHETIC BIOLOGY; PROTEIN SECRETION; EXPRESSION; STRATEGIES; SYSTEM; TRANSACTIVATORS; MODULATION; DEPLETION; CIRCUITS; DELIVERY;
D O I
10.1002/cbic.202300717
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
Synthetic or natural small molecules have been extensively employed as trigger signals or inducers to regulate engineered gene circuits introduced into living cells in order to obtain desired outputs in a controlled and predictable manner. Here, we provide an overview of small molecules used to drive synthetic-biology-based gene circuits in mammalian cells, together with examples of applications at different levels of control, including regulation of DNA manipulation, RNA synthesis and editing, and protein synthesis, maturation, and trafficking. We also discuss the therapeutic potential of these small-molecule-responsive gene circuits, focusing on the advantages and disadvantages of using small molecules as triggers, the mechanisms involved, and the requirements for selecting suitable molecules, including efficiency, specificity, orthogonality, and safety. Finally, we explore potential future directions for translation of these devices to clinical medicine. Small molecules have been widely utilized within the synthetic biology community as trigger input for regulating implemented genetic circuit in engineered mammalian cells. Here, we described the most commonly used small molecules and their associated genetic switches, employed to program cell behaviors, particularly within a cell and gene therapy context.image
引用
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页数:11
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