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生物分子浓度追踪器的设计与实现。

Design and implementation of a biomolecular concentration tracker.

作者信息

Hsiao Victoria, de los Santos Emmanuel L C, Whitaker Weston R, Dueber John E, Murray Richard M

机构信息

Division of Biology and Biological Engineering, California Institute of Technology , Pasadena, California United States.

出版信息

ACS Synth Biol. 2015 Feb 20;4(2):150-61. doi: 10.1021/sb500024b. Epub 2014 May 15.

Abstract

As a field, synthetic biology strives to engineer increasingly complex artificial systems in living cells. Active feedback in closed loop systems offers a dynamic and adaptive way to ensure constant relative activity independent of intrinsic and extrinsic noise. In this work, we use synthetic protein scaffolds as a modular and tunable mechanism for concentration tracking through negative feedback. Input to the circuit initiates scaffold production, leading to colocalization of a two-component system and resulting in the production of an inhibitory antiscaffold protein. Using a combination of modeling and experimental work, we show that the biomolecular concentration tracker circuit achieves dynamic protein concentration tracking in Escherichia coli and that steady state outputs can be tuned.

摘要

作为一个领域,合成生物学致力于在活细胞中构建日益复杂的人工系统。闭环系统中的主动反馈提供了一种动态且自适应的方式,以确保恒定的相对活性,而不受内在和外在噪声的影响。在这项工作中,我们使用合成蛋白质支架作为一种模块化且可调节的机制,通过负反馈进行浓度跟踪。电路的输入启动支架的产生,导致双组分系统的共定位,并产生一种抑制性抗支架蛋白。通过结合建模和实验工作,我们表明生物分子浓度跟踪电路在大肠杆菌中实现了动态蛋白质浓度跟踪,并且稳态输出可以进行调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d434/4384833/d6d2f457d53a/sb-2014-00024b_0002.jpg

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