C-RUI Collaborative Project: Intracellular and Structural Analysis of Roles of a Cytokine Precursor in Aminoacyl-tRNA Synthetase Complexes
C-RUI Collaborative Project: Intracellular and Structural Analysis of Roles of a Cytokine Precursor in Aminoacyl-tRNA Synthetase Complexes
批准号:
0215940
负责人:
Michael Hebert
金额:
$0.0万
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-09-01 至 2007-08-31
中文摘要
氨基酰基- trna合成酶复合物在蛋白质生物合成中起着关键作用。了解这些复合物及其变体的结构和分布是理解这一基本生物过程的机制和调控的基础,这一基本生物过程对细胞生长、维持和死亡具有重要影响。核心多合成酶复合物包含9个氨基酰基trna合成酶活性和3个辅助蛋白,p43、p38和p18。作为tRNA结合蛋白,p43可增强复合物内特定合成酶的氨基酰化活性。代谢应激诱导p43在caspase样位点的裂解以及该蛋白c端一半(EMAPII)的释放和分泌,其功能是炎症细胞因子。由于p43位于核心多酶氨基酰基- trna合成酶复合体的中心位置,p43的一个可能功能是维持该颗粒的结构完整性。该项目将确定代谢应激对p43切割和复合物稳定性的影响。具体来说,哺乳动物和非哺乳动物细胞将在各种不利条件下生长。将从这些培养物中纯化多合成酶复合物,并对其组成和结构进行表征。标记p43及其加工组分的复合物的细胞定位和分布将通过亚细胞组分的免疫印迹分析来定量。这项合作研究项目将主要由接受分子和结构生物学培训的本科生进行。
英文摘要
Aminoacyl-tRNA synthetase complexes play a key role in protein biosynthesis. An understanding of the structure and distribution of these complexes and their variants is fundamental to understanding the mechanisms and regulation of this basic biological process, which critically impacts cell growth, maintenance and death. The core multisynthetase complex contains nine aminoacyl-tRNA synthetase activities and three auxiliary proteins, p43, p38, and p18. A tRNA binding protein, p43 enhances aminoacylation activity of specific synthetases within the complex. Metabolic stress induces cleavage of p43 at a caspase-like site as well as release and secretion of the C-terminal half of the protein (EMAPII), which functions as an inflammatory cytokine. Due to its central location in the core multienzyme aminoacyl-tRNA synthetase complex, a likely function of p43 is to maintain structural integrity of this particle. This project will determine the effect of metabolic stress on p43 cleavage and stability of the complex. Specifically, mammalian and non-mammalian cells will be grown under various adverse conditions. Multisynthetase complexes will be purified from these cultures and their compositions and structures characterized. The cellular localization and distribution of complexes, of tagged p43 and of its processed components will be quantitated by immunoblot analysis of subcellular fractions. This collaborative research project will be performed primarily by undergraduate students who will receive training in molecular and structural biology.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Structural Analysis of the Multisynthetase Complex
-
批准号:0090539
-
项目类别:Standard Grant
-
资助金额:$0.0万
-
财政年份:2001
-
负责人:Michael Hebert
-
依托单位:
海外基金