PROJECT 4 - POLYPHENOLS AND DAMAGE IN THE EYE
PROJECT 4 - POLYPHENOLS AND DAMAGE IN THE EYE
批准号:
7558661
负责人:
STEPHEN BARNES
金额:
$19.82万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
AgingAging-Related ProcessAmino AcidsAnimal ModelAnimalsAntioxidantsAqueous HumorAromatic Amino AcidsAscorbic AcidBathingBiological AvailabilityBiological ModelsBiological PreservationBlindnessBotanicalsBudgetsCalmodulinCarotenoidsCataractCell NucleusCellsChemicalsChronicCrystallinsDietary PolyphenolDiseaseElectrophoresisEnvironmentEpithelial CellsEyeFellowshipFundingGlutathioneGrantHealthHeat shock proteinsHumanImpairmentIn VitroIntercellular FluidLeadLifeLightLightingMacular degenerationMass Spectrum AnalysisMeasuresMethodsMicrofluidic Analytical TechniquesMicrofluidicsModelingMolecular ChaperonesMutateMutationOrganOxygenPeptidesPhysiologicalPhytochemicalPlasmaPost-Translational Protein ProcessingPostdoctoral FellowPrecipitationPreparationPreventionProductionProteinsProteolysisQuality of lifeRattusReactionRecombinantsResearch PersonnelRestRoleSideSinglet OxygenSiteSunlightSurfaceTechniquesTimeVertebral columnVisionWorkage relatedaqueouscell watercrosslinkdietary supplementsin vitro Modelin vivointerestlenslens proteinmethionyltryptophanpolymerizationpolyphenolpreventprogramsresearch studysunlight-inducedtandem mass spectrometrytryptophyltyrosineultraviolet
中文摘要
眼睛中的蛋白质在维持人类生活质量方面发挥着至关重要的作用,特别是在衰老方面。其中有几种,比如晶状体蛋白,是一次性合成的,并在以后的生命中保存下来。由于它们暴露在bbb320 nm的光下,它们受到慢性阳光引起的损伤。这种损伤包括一些翻译后修饰和晶状体蛋白的交联,其程度尚不清楚。后者导致晶状体中蛋白质的沉淀,最终导致白内障的形成。单线态氧是一种重要的化学物质,它是由阳光的紫外线部分作用在眼睛中形成的。它与几个蛋白质氨基酸侧链(Cys, His, Met, Trp, Tyr)反应,引入氧原子。它还会在有限的位点引起肽主链的断裂。眼睛水中的局部化学环境,是一种浸泡在晶状体上的血浆超滤液,包括重要的抗氧化剂,如维生素C和谷胱甘肽。我们的假设是,来自植物膳食补充剂的多酚及其代谢物进入眼睛的水,从而协同增强其抗氧化环境。这是为了防止紫外光诱导的翻译后蛋白修饰和聚合,从而阻止与年龄相关的眼功能退化。在本建议中,我们将研究以下事项:(1)在大鼠模型中确定选定的植物多酚制剂对其在眼睛晶状体和房水中的组成的影响;(2)确定多酚对眼睛特定区域内源性抗氧化剂谷胱甘肽和外源性抗氧化剂维生素C和E以及类胡萝卜素水平的影响;(3)确定饮食多酚对晶状体晶体蛋白(一种具有伴侣活性的热休克蛋白)翻译后修饰和交联程度的影响;(4)利用体外模型蛋白和晶状体ab -晶体蛋白的特异性突变形式,研究单线态氧诱导的蛋白质切割和翻译后修饰的机制。这些实验将利用微流体分析和蛋白质质谱分析方面的技术和专业知识,这些技术和专业知识已在普渡大学- uab植物中心在之前的资助期间开发出来。他们将结合动物模型的体内实验和体外实验来研究单线态氧诱导蛋白质损伤的机制,以及特定多酚及其代谢物与生理抗氧化剂结合的作用。
英文摘要
The proteins in the eye perform a vital role in sustaining human quality of life, particularly with respect to aging. Several of them, such as the lens proteins, are synthesized one time and preserved for the rest of life. Since they are exposed to light > 320 nm, they are subject to chronic sunlight-induced damage. This damage includes several post-translational modifications and cross-linking of the lens proteins, the extent of which is poorly defined. The latter lead to precipitation of proteins in the lens and ultimately to cataract formation. An important chemical species that is formed in the eye by the action of the ultraviolet portion of sunlight is singlet oxygen. It reacts with several protein amino acid side chains (Cys, His, Met, Trp, Tyr) introducing oxygen atoms. It also causes cleavage of the peptide backbone at limited sites. The local chemical environment in the aqueous of the eye, an ultrafiltrate of plasma that bathes the lens, includes important antioxidant species such a vitamin C and glutathione. Our hypothesis is that polyphenols and their metabolites derived from botanical dietary supplements enter the aqueous of the eye and thereby synergistically enhance its anti-oxidant environment. This is proposed to prevent UV light-induced post-translational protein modification and polymerization and therefore deter age-related degeneration of eye function. In this proposal, we will examine the following: (1) to determine in a rat model the effect of selected botanical polyphenol preparations on their composition in the lens and aqueous humor of the eye, (2) to determine the effects of polyphenols on the levels of the endogenous antioxidant glutathione and the exogenous antioxidants vitamins C and E and carotenoids in specific regions of the eye, (3) to determine the effects of dietary polyphenols on the extent of post-translational modifications and cross-linking of the lens acrystallin (a heat shock protein with chaperone activity), and (4) use specifically mutated forms of a model protein in vitro and lens aB-crystallin to examine the mechanism of singlet oxygen-induced protein cleavage and posttranslational modifications. These experiments will utilize techniques and expertise in microfluidics analysis and protein mass spectrometry that have been developed in the Purdue-UAB Botanicals Center in the previous grant period. They will use a combination of in vivo experiments in animal models and in vitro experiments to examine the mechanisms of singlet oxygen-induced protein damage and the role of specific polyphenols and their metabolites in combination with physiological antioxidants.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
"UAB Metabolomics Workshop: from design to decision"
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批准号:8717686
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项目类别:
-
资助金额:$10.8万
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财政年份:2012
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负责人:STEPHEN BARNES
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依托单位:
"UAB Metabolomics Workshop: from design to decision"
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批准号:8416292
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项目类别:
-
资助金额:$5.4万
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财政年份:2012
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负责人:STEPHEN BARNES
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依托单位:
"UAB Metabolomics Workshop: from design to decision"
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批准号:8912500
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项目类别:
-
资助金额:$10.8万
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财政年份:2012
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负责人:STEPHEN BARNES
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依托单位:
Lens crystallins: spatial location and properties in the ICR/f rat cataract model
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批准号:7976943
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项目类别:
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资助金额:$23.03万
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财政年份:2010
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负责人:STEPHEN BARNES
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依托单位:
Lens crystallins: spatial location and properties in the ICR/f rat cataract model
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批准号:8134148
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项目类别:
-
资助金额:$0.81万
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财政年份:2010
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负责人:STEPHEN BARNES
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依托单位:
5500 Q-Trap Mass Spectrometer
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批准号:7794200
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项目类别:
-
资助金额:$46.92万
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财政年份:2010
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负责人:STEPHEN BARNES
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依托单位:
Lens crystallins: spatial location and properties in the ICR/f rat cataract model
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批准号:8117497
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项目类别:
-
资助金额:$17.91万
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财政年份:2010
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负责人:STEPHEN BARNES
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依托单位:
Skin Proteomics Core
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批准号:7677162
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项目类别:
-
资助金额:$12.17万
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财政年份:2009
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负责人:STEPHEN BARNES
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依托单位:
Urinary peptide excretion and onset of puberty
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批准号:7846995
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项目类别:
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资助金额:$13.34万
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财政年份:2009
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负责人:STEPHEN BARNES
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依托单位:
Bioanalytical CoreBioanalytical Core
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批准号:8899511
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项目类别:
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资助金额:$23.12万
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财政年份:2008
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负责人:STEPHEN BARNES
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依托单位:
Urinary peptide excretion and onset of puberty
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批准号:7624986
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项目类别:
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资助金额:$18.13万
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财政年份:2008
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负责人:STEPHEN BARNES
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依托单位:
Bioanalytical CoreBioanalytical Core
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批准号:8733667
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项目类别:
-
资助金额:$23.12万
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财政年份:2008
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负责人:STEPHEN BARNES
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依托单位:
Urinary peptide excretion and onset of puberty
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批准号:7486047
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项目类别:
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资助金额:$22.88万
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财政年份:2008
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负责人:STEPHEN BARNES
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依托单位:
Core C - Bioanalytical Resource Core
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批准号:10252039
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项目类别:
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资助金额:$23.02万
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财政年份:2008
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负责人:STEPHEN BARNES
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依托单位:
Core C - Bioanalytical Resource Core
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批准号:10456260
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项目类别:
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资助金额:$23.02万
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财政年份:2008
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负责人:STEPHEN BARNES
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依托单位:
Bioanalytical CoreBioanalytical Core
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批准号:8625448
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项目类别:
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资助金额:$23.12万
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财政年份:2008
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负责人:STEPHEN BARNES
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依托单位:
Bioanalytical CoreBioanalytical Core
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批准号:9334186
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项目类别:
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资助金额:$22.89万
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财政年份:2008
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负责人:STEPHEN BARNES
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依托单位:
IN VIVO BIOAVAILABILITY CORE
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批准号:6954988
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项目类别:
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资助金额:$18.46万
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财政年份:2005
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负责人:STEPHEN BARNES
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依托单位:
PROJECT 4 - POLYPHENOLS AND DAMAGE IN THE EYE
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批准号:6954994
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项目类别:
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资助金额:$15.78万
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财政年份:2005
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负责人:STEPHEN BARNES
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依托单位:
MASS SPECT: ASTHMA, LUNG INJURY & MYCOPLASM PULMONIS
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批准号:6973455
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项目类别:
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资助金额:$9.3万
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财政年份:2004
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负责人:STEPHEN BARNES
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依托单位: