Developing a synthetic signalling system capable of the precise spatial and temporal control of protein function in living cells
Developing a synthetic signalling system capable of the precise spatial and temporal control of protein function in living cells
批准号:
MR/T021144/1
负责人:
Byron Carpenter
金额:
$133.29万
依托单位:
依托单位国家:
英国
项目类别:
Fellowship
财政年份:
2020
资助国家:
英国
项目状态:
已结题
起止时间:
2020 至 --
中文摘要
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英文摘要
The aim of synthetic biology is to modify cells or biological systems in ways that produce societal and economic benefits in the areas of healthcare, energy production, food security and the environment. Eukaryotic cells hold huge potential in synthetic biology, however, due to their complexity, modifying them using conventional synthetic biology approaches, which involve constructing gene networks, is challenging. In contrast, directly regulating the function of proteins inside these cells may offer a simpler method to control their behaviour. A number of options, including antibodies, are currently available to do this, but the drawback of these approaches is that they cannot be easily switched off, so they affect the cell's behaviour continuously. In order to control cell behaviour more precisely, we need to develop a new system that can be turned on or off rapidly. The Ideal system would comprise a switch-like 'effector' protein inside the cell that can be engineered to bind and regulate other proteins, and a 'receptor' protein on the cell surface that can switch the effector protein on when a specific chemical is added to its environment. G protein-coupled receptor (GPCR) signalling pathways are natural systems that cells use to communicate; they are therefore ideal templates for the development of a new tool to control cell behaviour. GPCRs are cell-surface receptors that detect chemicals outside the cell, and activate effector proteins, called 'G proteins', inside the cell. The G proteins act as switches, which, when activated by GPCRs, bind and regulate their target protein, before switching themselves off in a time-dependent manner. Until now, it has not been possible to modify G proteins to bind and regulate different cellular proteins because of the high degree of complexity that has evolved within these pathways. However, I recently developed a simplified G protein that may, for the first time, make this possible.This proposal aims to modify the GPCR signalling pathway to create a novel cell-based tool that will allow us to control the activity of different proteins inside live eukaryotic cells. This will enable us to either study the protein's function in real time or directly control cellular processes and behaviours. The key component of this system will be the simplified G protein, which will be modified so that it can bind and regulate different cellular proteins. This G protein can be activated by either native GPCRs, in which case the tool could be controlled using naturally occurring chemicals (such as a hormone), or a modified GPCR, in which case it could be controlled by a specially designed chemical. This tool will have applications in several different areas. First, it will underpin basic research to understand the function of native cellular proteins that are central to the health and disease of animals and humans. Second, it will have applications in the development of a range of cell-based biosensors capable of detecting hundreds of physiologically-relevant chemicals in real time. Third, it will facilitate research in the field of regenerative medicine, by facilitating the precise control of human cell behaviour, for example, cell division. The first four years of the Fellowship will be used to develop and optimise the tool, and to foster partnerships with companies that are capable of translating it into viable healthcare products. The final three years will focus on both developing the biosensor applications, with the aim of producing miniaturised medical diagnostic devices, and exploring applications to control human cell division, with the aim of developing improved treatments for degenerative conditions such as osteoarthritis. The long-term implication of this research will be a novel cell-based tool that will benefit both academic and industrial researchers, by simplifying the implementation of synthetic biology in eukaryotic cells and expediting its promised societal and economic benefits.
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国内基金
海外基金
近空间飞行器载MIMO SAR高分辨率、宽测绘带遥感成像机理与方法
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批准号:41101317
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项目类别:青年科学基金项目
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资助金额:25.0万元
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批准年份:2011
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负责人:王文钦
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依托单位:
基于大机动运动平台的特定目标多极化成像与匹配技术研究
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批准号:11176022
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项目类别:联合基金项目
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资助金额:46.0万元
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批准年份:2011
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负责人:周峰
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依托单位: