Chemical/biochemical tools for studying novel protein acyl lysine modifications
Chemical/biochemical tools for studying novel protein acyl lysine modifications
批准号:
8546409
负责人:
Hening Lin
金额:
$52.63万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-17 至 2016-08-31
关键词:
Acetyl Coenzyme AAcetylationAcetyltransferaseAcylationAddressAffinityAntibodiesApoptosisBiochemicalBiologicalBiological ProcessBiologyCellsChemicalsChemistryDeacetylaseDevelopmentDrug TargetingEnzymesEpigenetic ProcessGene ExpressionGoalsHistonesIndividualKnock-outLaboratoriesLysineMalignant NeoplasmsMammalian CellMammalsMetabolicMetabolismMethodsModificationPathway interactionsPeptidesPlayPost-Translational Protein ProcessingProcessProtein AcetylationProteinsReagentRegulationRelative (related person)ResearchRoleSirtuinsSiteTestingTranscriptional RegulationTransferaseVorinostatWarburg EffectWestern Blottingacyl groupanalogbiological systemsfatty acylationhuman diseaseinhibitor/antagonistinsightinterestnovelnovel therapeuticsprotein functionprotein metabolismtherapeutic targettool
中文摘要
描述(由申请人提供):蛋白质翻译后修饰对于调节蛋白质功能非常重要,并且涉及许多生物过程。蛋白质乙酰化由乙酰转移酶和去乙酰化酶控制,在转录和代谢调节中起重要作用。乙酰基供体乙酰辅酶a是细胞中的代谢中间体。最近,我们的实验室发现了几种新的酰基赖氨酸修饰,它们在结构上与乙酰基非常不同。我们已经证明,这些新的酰基赖氨酸修饰发生在哺乳动物细胞中,并且有专门的酶(sirtuins)可以有效地去除它们。与乙酰化一样,这些新的酰基赖氨酸修饰也来自于常见的代谢中间体,这表明这些修饰可能是一种感知代谢调节蛋白质功能的机制。研究这些新的修饰将使我们更好地了解生物系统的化学性质。这项研究有可能为蛋白质乙酰化领域的一些难题提供答案,比如大约一半的蛋白质去乙酰化酶缺乏酶活性。因为这些酰基赖氨酸修饰以前没有被研究过,所以没有工具可以用来研究它们。多种酰基赖氨酸修饰的存在也为这些修饰的研究增加了一层技术复杂性。本提案的目标是开发新的和更好的方法来检测和量化这些修饰,然后使用这些方法来研究这些修饰的发生,调节和功能。
英文摘要
DESCRIPTION (provided by applicant): Protein posttranslational modifications are important for regulating protein function and are involved in numerous biological processes. Protein acetylation, controlled by acetyltransferases and deacetylases, are known to play important roles in regulation of transcription and metabolism. The acetyl donor, acetyl-CoA, is a metabolic intermediate in cells. Recently, our laboratory discovered several novel acyl lysine modifications that are structurally very different from acetyl. We have shown that these new acyl lysine modifications occur in mammalian cells and there are dedicated enzymes (sirtuins) that can remove them efficiently. These new acyl lysine modifications, like acetylation, also come from common metabolic intermediates, suggesting that these modifications may be a mechanism of sensing metabolism to regulate protein function. Studying these new modifications will allow us to better understand the chemistry of biological systems. The study has the potential to provide answers to a number of puzzles in the protein acetylation field, such as the lack of enzymatic activity for about half of the protein deacetylases. Because these acyl lysine modifications have not been studied before, no tools are available to investigate them. The existence of multiple acyl lysine modifications also adds a layer of technical complexity to the study of these modifications. The goal of this proposal is to develop new and better methods to detect and quantify these modifications and then use these methods to investigate the occurrence, regulation, and function of these modifications.
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