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A novel function for translation initiation factor eIF5

A novel function for translation initiation factor eIF5
翻译起始因子 eIF5 的新功能
批准号:
BB/E002005/1
负责人:
Graham Pavitt
金额:
$36.71万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2007
资助国家:
英国
项目状态:
已结题
起止时间:
2007 至 --

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中文摘要
翻译
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英文摘要
Interactions between proteins modulate essential functions of cells ensuring that they can grow and perform their tasks at the correct time and place. Each protein within a cell is like a piece within a complex machine. In a machine each part must be in the correct place and act at the correct time in concert with the other parts for the machine to function properly. The same is true for proteins within cells, but unlike most machines and their parts, proteins are continually renewed, move and can be modified by interaction with many other cell components to alter their function and/or location. Many proteins act together within complexes composed of proteins or with other cell components (lipids, DNA or small molecules for example) to coordinate a common function. One group of proteins relevant to this proposal is required make (or synthesize) all new proteins in each cell. These are called 'protein synthesis factors'. Understanding how protein synthesis factors function and interact with each other is therefore fundamental to understanding how proteins are made in all cells in all organisms. By improving our understanding how processes such as protein synthesis work in normal cells it can help scientists understand diseases in which this process is altered, or how infectious agents such as viruses are able to hijack plant, animal or human cells and cause infectious diseases. In work leading up to this proposal we have identified a novel complex between two protein synthesis factors known as eIF2 and eIF5. This has lead to a hypothesis for the function of this complex which we intend to assess here using a combination of biochemical experiments with purified proteins 'in the test-tube' and genetic experiments using yeast cells as a model simple cell system to understand the biological significance of this interaction for the mechanism and regulation of protein synthesis.
期刊论文(7)
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DOI: 10.1093/nar/gkr339
发表时间: 2011-10
期刊: Nucleic acids research
影响因子: 14.9
作者: [Singh CR, Watanabe R, Zhou D, Jennings MD, Fukao A, Lee B, Ikeda Y, Chiorini JA, Campbell SG, Ashe MP, Fujiwara T, Wek RC, Pavitt GD, Asano K]
通讯作者: Asano K
DOI: 10.1186/gb-2008-9-10-323
发表时间: 2008-10-21
期刊: Genome biology
影响因子: 12.3
作者: [Pavitt GD, Ashe MP]
通讯作者: Ashe MP
Erratum: eIF5 has GDI activity necessary for translational control by eIF2 phosphorylation
勘误:eIF5 具有 eIF2 磷酸化翻译控制所需的 GDI 活性
DOI: 10.1038/nature09550
发表时间: 2010
期刊: Nature
影响因子: 64.8
作者: [Jennings M]
通讯作者: Jennings M
DOI: 10.4161/sgtp.1.2.13783
发表时间: 2010-09-01
期刊: Small GTPases
影响因子: --
作者: [Jennings, Martin D, Pavitt, Graham D]
通讯作者: Pavitt, Graham D
Quantitative dissection of protein synthesis initiation at 'omic and single mRNA scales
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    2023
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  • 依托单位:
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    2019
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    2016
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    2015
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