NMR and DFT Investigation of Porphyrin Conformation in Cytochromes c
细胞色素 c 中卟啉构象的 NMR 和 DFT 研究
基本信息
- 批准号:8080235
- 负责人:
- 金额:$ 1.12万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-06-01 至 2011-07-31
- 项目状态:已结题
- 来源:
- 关键词:Biochemical ProcessBiologicalBiological ModelsBiological ProcessBiologyCatalysisCell NucleusChemicalsCircular DichroismComputing MethodologiesCrystallizationDNA Sequence RearrangementDataData ReportingDevelopmentDiseaseElectron Spin Resonance SpectroscopyElectron TransportElectronicsFamilyFutureGasesGoalsHealthHemeHemeproteinsHumanHydrogen BondingInvestigationLabelLinkMeasuresMethodsMolecular ConformationMutationNMR SpectroscopyNuclear Magnetic ResonanceOrganismOxygenPorphyrinsPositioning AttributeProcessPropionatesProtein FamilyProteinsPyrrolesRaman Spectrum AnalysisResearch ProposalsSamplingShapesSideSolutionsStructureSystemTechniquesUnited States National Institutes of HealthVariantX-Ray Crystallographyabsorptionbasebiological systemscofactorcovalent bondcytochrome cdensityelectronic structureoxygen transportpolypeptideresearch studysmall moleculestructural biologytheoriestool
项目摘要
DESCRIPTION (provided by applicant): The long-term objective of this project is to develop the first experimental tool capable of quantitatively measuring the conformation of heme in solution. This tool will be an important contribution to the structural biology initiative of the NIH roadmap, which could be used in future studies that determine the nuclear magnetic resonance (NMR) solution structure of heme proteins. Heme proteins have a diverse set of biological functions, including: electron transport, gas transport, small molecule sensing, and catalysis. Each heme protein optimizes the reactivity of the heme cofactor to achieve its specific function and heme conformation is arguably the most under-investigated strategy available. It is essential to understand this determinant of heme electronic structure and reactivity to fully comprehend the biochemical processes involving heme proteins, and diseases associated with their malfunction. The cytochrome c family of proteins will be used as a model system to develop this tool because this family utilizes a nonplanar heme cofactor and the protein matrix provides a strategy to alter the heme conformation in a systematic way that is unlikely to introduce large-scale protein conformational changes. Paramagnetic 1H and 13C NMR spectroscopy will be used as a spectroscopic probe because this technique can simultaneously examine the electronic structure of heme at several positions on the porphyrin macrocycle. Multi-dimensional NMR experiments and selective isotopic enrichment of the heme cofactor will be used to make heme paramagnetic 1H and 13C resonance assignments. Density functional theory (DFT) calculations, initially assisted by X-ray crystallography and resonance Raman spectroscopy, will be used to interpret the paramagnetic NMR data in terms of out-of-plane distortions of the heme cofactor. Ultimately, this strategy will produce a DFT-based correlation between paramagnetic NMR data and heme conformation. This new tool can be applied to a wide range of heme proteins that have important functions within biological systems. The DFT-based correlation will also identify the relationship between heme conformation, electronic structure, and reactivity. PUBLIC HEALTH RELEVANCE: Biological organisms, including humans, use heme to carry out a diverse set of fundamental processes. To maximize the efficiency of a specific process, biological systems manipulate heme and its surroundings. Arguably, the most under-investigated manipulation available to heme proteins is changing the shape, and this proposal will develop the first method to measure the shape of heme in solution.
描述(由申请人提供):该项目的长期目标是开发第一个能够定量测量溶液中血红素构象的实验工具。该工具将是对NIH路线图的结构生物学计划的重要贡献,该计划可用于确定血红素蛋白的核磁共振(NMR)溶液结构的未来研究。血红素蛋白具有多种生物学功能,包括:电子传输,气体传输,小分子传感和催化。每种血红素蛋白都优化了血红素辅因子以达到其特定功能的反应性,而血红素构象可以说是可用的最不受欢迎的策略。必须了解血红素电子结构和反应性的决定因素,以完全理解涉及血红素蛋白的生化过程以及与其故障相关的疾病。细胞色素C家族将用作开发该工具的模型系统,因为该家族使用非平面血红素辅因子,而蛋白质基质则提供了一种以系统的方式改变血红素构象的策略,这种策略不太可能引入大型蛋白质构象变化。顺磁1H和13C NMR光谱将用作光谱探针,因为该技术可以同时检查卟啉大环上多个位置的血红素的电子结构。多维NMR实验和血红素辅因子的选择性同位素富集将用于使血红素顺磁1H和13C共振分配。最初由X射线晶体学和共振拉曼光谱辅助的密度功能理论(DFT)计算将以血红素辅助因子的平面畸变来解释顺磁性NMR数据。最终,该策略将在顺磁NMR数据和血红素构象之间产生基于DFT的相关性。该新工具可以应用于在生物系统中具有重要功能的多种血红素蛋白。基于DFT的相关性还将确定血红素构象,电子结构和反应性之间的关系。公共卫生相关性:包括人类在内的生物生物使用血红素进行多种基本过程。为了最大程度地提高特定过程的效率,生物系统操纵血红素及其周围环境。可以说,血红素蛋白可用的最不足的操纵正在改变形状,该建议将开发出第一种测量溶液中血红素形状的方法。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Matthew D Liptak其他文献
Matthew D Liptak的其他文献
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{{ truncateString('Matthew D Liptak', 18)}}的其他基金
Heme Oxygenases: chemically complex enzymes found in diverse biological pathways
血红素加氧酶:在多种生物途径中发现的化学复合酶
- 批准号:
10356808 - 财政年份:2021
- 资助金额:
$ 1.12万 - 项目类别:
Heme Oxygenases: chemically complex enzymes found in diverse biological pathways
血红素加氧酶:在多种生物途径中发现的化学复合酶
- 批准号:
10578804 - 财政年份:2021
- 资助金额:
$ 1.12万 - 项目类别:
Second-Sphere Influences on Oxygen Activation by Non-Canonical Heme Oxygenases
第二领域对非典型血红素加氧酶的氧活化的影响
- 批准号:
9750001 - 财政年份:2016
- 资助金额:
$ 1.12万 - 项目类别:
Second-Sphere Influences on Oxygen Activation by Non-Canonical Heme Oxygenases
第二领域对非典型血红素加氧酶的氧活化的影响
- 批准号:
9979903 - 财政年份:2016
- 资助金额:
$ 1.12万 - 项目类别:
Second-Sphere Influences on Oxygen Activation by Non-Canonical Heme Oxygenases
第二领域对非典型血红素加氧酶的氧活化的影响
- 批准号:
9981995 - 财政年份:2016
- 资助金额:
$ 1.12万 - 项目类别:
NMR and DFT Investigation of Porphyrin Conformation in Cytochromes c
细胞色素 c 中卟啉构象的 NMR 和 DFT 研究
- 批准号:
7871457 - 财政年份:2009
- 资助金额:
$ 1.12万 - 项目类别:
NMR and DFT Investigation of Porphyrin Conformation in Cytochromes c
细胞色素 c 中卟啉构象的 NMR 和 DFT 研究
- 批准号:
7750822 - 财政年份:2009
- 资助金额:
$ 1.12万 - 项目类别:
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