Scaling up genetic circuit design for cellular computing: advances and prospects

被引:47
|
作者
Xiang, Yiyu [1 ,2 ]
Dalchau, Neil [3 ]
Wang, Baojun [1 ,2 ]
机构
[1] Univ Edinburgh, Sch Biol Sci, Edinburgh EH9 3FF, Midlothian, Scotland
[2] Univ Edinburgh, Ctr Synthet & Syst Biol, Edinburgh EH9 3JR, Midlothian, Scotland
[3] Microsoft Res, Cambridge CB1 2FB, England
基金
英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会;
关键词
Cellular computing; Synthetic biology; Genetic circuit; Genetic logic gates; Analog computation; Biodesign automation; BIOLOGY MARKUP LANGUAGE; RNA-BINDING PROTEINS; SYNTHETIC BIOLOGY; METABOLIC BURDEN; LOGIC GATES; TRANSCRIPTION FACTORS; COMPUTATION; EXPRESSION; NETWORK; CONSTRUCTION;
D O I
10.1007/s11047-018-9715-9
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Synthetic biology aims to engineer and redesign biological systems for useful real-world applications in biomanufacturing, biosensing and biotherapy following a typical design-build-test cycle. Inspired from computer science and electronics, synthetic gene circuits have been designed to exhibit control over the flow of information in biological systems. Two types are Boolean logic inspired TRUE or FALSE digital logic and graded analog computation. Key principles for gene circuit engineering include modularity, orthogonality, predictabilityand reliability. Initial circuits in the field were small and hampered by a lack of modular and orthogonal components, however in recent years the library of available parts has increased vastly. New tools for high throughput DNA assembly and characterization have been developed enabling rapid prototyping, systematic in situ characterization, as well as automated design and assembly of circuits. Recently implemented computing paradigms in circuit memory and distributed computing using cell consortia will also be discussed. Finally, we will examine existing challenges in building predictable large-scale circuits including modularity, context dependency and metabolic burden as well as tools and methods used to resolve them. These new trends and techniques have the potential to accelerate design of larger gene circuits and result in an increase in our basic understanding of circuit and host behaviour.
引用
收藏
页码:833 / 853
页数:21
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