NMR and DFT Investigation of Porphyrin Conformation in Cytochromes c

描述(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。这一工具将对NIH路线图的结构生物学倡议做出重要贡献，可用于未来确定血红素蛋白质的核磁共振(核磁共振)溶液结构的研究。血红素蛋白具有多种生物学功能，包括：电子传递、气体传递、小分子传感和催化作用。每种血红素蛋白都优化了血红素辅因子的反应能力，以实现其特定的功能，而血红素构象可以说是目前研究最少的策略。了解血红素电子结构和反应性的决定因素对于全面理解涉及血红素蛋白的生化过程以及与其功能障碍相关的疾病是至关重要的。细胞色素c蛋白质家族将被用作开发这一工具的模型系统，因为该家族利用了一种非平面的血红素辅助因子，而蛋白质基质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规模的蛋白质构象变化。顺磁~1H和~(13)C核磁共振谱将被用作光谱探针，因为这项技术可以同时检测血红素在卟啉大环上的几个位置的电子结构。多维核磁共振实验和选择性同位素浓缩的血红素辅因子将被用来进行血红素顺磁性的1H和13C共振归属。密度泛函理论(DFT)计算，最初由X射线结晶学和共振拉曼光谱辅助，将被用来解释顺磁核磁共振数据，根据血红素辅因子的平面外扭曲。最终，这一策略将在顺磁核磁共振数据和血红素构象之间产生基于密度泛函的关联。这一新工具可以应用于在生物系统中具有重要功能的广泛的血红素蛋白。基于密度泛函理论的相关性也将确定血红素构象、电子结构和反应性之间的关系。与公共卫生相关：包括人类在内的生物有机体使用血红素进行一系列不同的基本过程。为了最大限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，对血红素蛋白质最未被研究的操作是改变形状，这一提议将开发第一种测量溶液中血红素形状的方法。

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.