In vivo protein-based biosensors: seeing metabolism in real time

被引:9
|
作者
Alexandrov, Kirill [1 ,2 ]
Vickers, Claudia E. [1 ,2 ,3 ,4 ]
机构
[1] Queensland Univ Technol, ARC Ctr Excellence Synthet Biol, Ctr Agr & Bioecon,Sch Biol & Environm Sci, Ctr Genom & Personalised Hlth,CSIRO QUT Synthet Bi, Brisbane, Qld 4001, Australia
[2] Commonwealth Sci & Ind Res Org CSIRO, CSIRO Future Sci Platform Synthet Biol, Dutton Pk, Brisbane, Qld 4012, Australia
[3] Eden Brew, Brisbane, Qld 4001, Australia
[4] Griffith Univ, Griffith Inst Drug Discovery, Brisbane, Qld 4111, Australia
基金
澳大利亚研究理事会;
关键词
FLUORESCENT; DESIGN; ENZYMES; EVOLUTION;
D O I
10.1016/j.tibtech.2022.07.002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Biological homeostasis is a dynamic and elastic equilibrium of countless interlinked biochemical reactions. A key goal of life sciences is to understand these dynamics; bioengineers seek to reconfigure such networks. Both goals require the ability to monitor the concentration of individual intracellular metabo-lites with sufficient spatiotemporal resolution. To achieve this, a range of protein or protein/DNA signalling circuits with optical readouts have been constructed. Protein biosensors can provide quantitative information at subsecond temporal and suborganelle spatial resolution. However, their construction is fraught with difficulties related to integrating the affinity-and selectivity-endowing com-ponents with the signal reporters. We argue that development of efficient approaches for construction of chemically induced dimerisation systems and reporter domains with large dynamic ranges will solve these problems.
引用
收藏
页码:19 / 26
页数:8
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