Establishment of methods for prediction of the function of functionally-unknown gene products by the analysis of the posttranslational protein modifications.
Establishment of methods for prediction of the function of functionally-unknown gene products by the analysis of the posttranslational protein modifications.
批准号:
15580080
负责人:
UTSUMI Toshihiko
金额:
$2.5万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2004
中文摘要
随着人类基因组计划的完成,现在已经有了大量的基因序列。然而,这些基因中的许多功能还没有确定。因此,鉴定这些基因的功能是蛋白质组学研究的重要目的之一。目前,众所周知,许多翻译后修饰,如蛋白质降解加工、磷酸化、糖基化、脂质修饰、ADP核糖化等,在蛋白质的结构和功能中起着关键作用,并调节许多细胞事件,如细胞内信号转导。然而,目前还没有建立系统的方法来分析蛋白质的翻译后修饰。在本研究中,我们已经证明,在体外翻译系统或在转基因细胞中,利用代谢标记可以成功地检测到不同蛋白质的靶向、加工和修饰。由于许多这些翻译后修饰在蛋白质的结构和功能中扮演着特定的角色,因此从这些实验观察中预测蛋白质的功能是可能的。
英文摘要
Upon the completion of the Human Genome Project, huge numbers of genetic sequences are now available. However, the function of many of these genes has not been identified. Therefore, the identification of the function of these genes is one of the most important purposes of the study of Proteomics.Now, it is well known that many of the posttranslational modifications such as proteolytic processing, phosphorylation, glycosylation, lipid modifications, ADP-ribosylation etc. play critical roles in the structure and function of protein and regulate many cellular events such as intracellular signal transduction. However, systematic method to analyze the posttranslational modification of protein has not been established.In the present study, we have shown that targeting, processing and modification of a distinct protein could be successfully detected by using metabolic labeling in an in vitro translation system or in transfected cells. Since many of these posttranslational modifications play specific roles in the structure and function of protein, it might be possible to predict the function of the protein from these experimental observations.
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Utsumi, T. et al.: "Vertical-scanning mutagenesis of amino acids in a model N-myristoylation motif reveals the major amino-terminal sequence requirements for protein N-myristoylation"Eur.J.Biochem.. 271. 863-874 (2004)
Utsumi, T. 等人:“模型 N-肉豆蔻酰化基序中氨基酸的垂直扫描诱变揭示了蛋白质 N-肉豆蔻酰化的主要氨基末端序列要求”Eur.J.Biochem.. 271. 863-874(
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通讯作者:
内海俊彦: "「膜局在性のタンパク質工学的改変による生理活性タンパク質の機能変換」タンパク質工学"医学書院. 165-204 (2003)
Toshihiko Utsumi:“通过膜定位蛋白质工程修饰实现生理活性蛋白质的功能转换”蛋白质工程,Igaku Shoin 165-204(2003)。
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N-ミリストイル化によるタンパク質の膜局在化と機能調節
N-肉豆蔻酰化对蛋白质的膜定位和功能调节
DOI:
--
发表时间:
2004
期刊:
実験医学 22
影响因子:
--
作者:
[Utsumi, T. et al., 内海俊彦]
通讯作者:
内海俊彦
Topogenesis of two transmembrane type K+ channels, Kir 2.1 and Kcs A
两种跨膜 K 型通道 Kir 2.1 和 Kcs A 的拓扑发生
DOI:
--
发表时间:
2003
期刊:
J.Biol.Chem. 278
影响因子:
--
作者:
[Umigai, N., et al.]
通讯作者:
et al.
In vitro及びin vivo代謝標識法を用いた蛋白質翻訳後修飾の解析
使用体外和体内代谢标记方法分析蛋白质翻译后修饰
DOI:
--
发表时间:
2003
期刊:
生化学 75
影响因子:
--
作者:
[Umigai, N. et al., 内海俊彦]
通讯作者:
内海俊彦
共 18 条
Analysis of novel regulatory mechanism of apoptosis mediated by the posttranslational N-myristoylation of protein
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批准号:20580099
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.08万
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财政年份:2008
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负责人:UTSUMI Toshihiko
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依托单位:
A novel mechanism for the regulation of cellular apoptosis mediated by posttranslational N-myristoylation of cytoskeletal proteins.
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批准号:17580080
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.37万
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财政年份:2005
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负责人:UTSUMI Toshihiko
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依托单位:
Molecular mechanism of cellular processing of transmembrane tumor necrosis factor
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批准号:12660080
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.3万
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财政年份:2000
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负责人:UTSUMI Toshihiko
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依托单位:
Molecular mechanism of cellular processing of tumor necrosis factor (TNF)
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批准号:10660092
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.37万
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财政年份:1998
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负责人:UTSUMI Toshihiko
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依托单位:
Preparation and characterization of an N-myristoylated fusion protein that binds to the membrane surface
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批准号:06660112
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项目类别:Grant-in-Aid for General Scientific Research (C)
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资助金额:$1.34万
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财政年份:1994
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负责人:UTSUMI Toshihiko
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依托单位:
海外基金