CYTOCHROME P450 INTERACTION W/ CYTOCHROME B5: NMR

细胞色素 P450 与细胞色素 B5 的相互作用：NMR

• 批准号: 6220206
• 负责人: VLADIMIR J BASUS
• 金额: $ 0.16万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-07-01 至 2000-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6220206
• 关键词: aging; biological products; biomedical resource; genome; growth /development; lymphatic system; model design /development; nervous system; proteins

Our overall long-term goal of this project is to understand the molecular basis of the effect of cytochrome b5 (cyt b5) on the metabolism of certain substrates by cytochrome P450 (cyt P450), and to determine the physiological significance of this reaction. In particular, we are interested in elucidating the molecular basis of the marked stimulatory effect of cyt b5 on the metabolism of the volatile anesthetic, methoxyflurane, by cyt P450 LM2 (2B4). These studies may eventually lead to the delineation of the etiology and pathophysiology of the postoperative hepatotoxicity attributed to the volatile anesthetics and to the development of safer anesthetics. These studies should also provide important information about the mechanism by which cyt P450 oxidizes its numerous endogenous and xenobiotic substrates. This knowledge should prove valuable in facilitating the design of clinically useful inhibitors of cytochrome P450 for therapeutic applications in fungal diseases, hyperaldosteronism, prostate cancer, benign prostatic hypertrophy and breast cancer. The more immediate goal of our proposal is to use the 23,000 dalton cyt b5-cytochrome c (cyt c) complex as a model for the larger (72,000 dalton) hydrophobic cyt b5-cyt P450 complex and determine the structure of the model complex using high resolution NMR. The cytochrome b5-cytochrome c complex is a relevant model for the larger hydrophobic complex because cytochrome b5 uses approximately the same site to interact with both cytochrome c and cytochrome P450. Knowledge of the structure of the cyt b5-cyt c complex will provide insights into 1) the mechanism, 2) pathway of electron transfer, between cyt b5 and its redox partners and 3) macromolecular recognition and protein dynamics. The computing, graphics and programming facilities at the UCSF Computer Laboratory have been and will be used to construct three-dimensional molecular models based on results from our NMR studies, to display and examine these models, and to calculate the dynamics and interactions of the components in the models. These results should lead to a greater understanding of some the structural basis for the requirement for cyt b5 for the metabolism of some substrates by cyt P450.

我们这个项目的总体长期目标是了解 细胞色素b5(Cytb5)影响细胞周期的分子基础 细胞色素P450(Cyt P450)对某些底物的代谢 确定这一反应的生理意义。在……里面 特别是，我们感兴趣的是阐明 细胞色素b5对细胞的代谢有明显的促进作用 挥发性麻醉剂，甲氧氟烷，由细胞色素P450 LM2(2B4)。这些 研究可能最终导致描述病因学和 术后肝毒性的病理生理学研究 挥发性麻醉药和更安全麻醉药的开发。 这些研究还应提供有关 细胞色素P450氧化其众多内源性和 异源生物基质。这一知识应该被证明在 促进临床上有用的细胞色素抑制剂的设计 P450在真菌疾病治疗中的应用， 醛固酮增多症、前列腺癌、良性前列腺肥大和 乳腺癌。我们提议的更直接的目标是使用 23,000道尔顿细胞色素b5-细胞色素c(Cytc)复合体作为 更大的(72,000道尔顿)疏水性细胞色素b5-细胞色素P450复合体和 使用高分辨率确定模型复合体的结构 核磁共振。细胞色素b5-细胞色素c复合体是 更大的疏水复合体，因为细胞色素b5使用 与细胞色素c和细胞色素c相互作用的位置大致相同 细胞色素P450。对cyt b5-cyt c结构的了解 复合体将提供对1)机制，2)途径的洞察 Cyt b5与其氧化还原伙伴和3之间的电子转移 大分子识别和蛋白质动力学。计算， 加州大学旧金山分校计算机实验室的图形和编程设施 已经并将被用来构建三维分子 基于我们的核磁共振研究结果的模型，以显示和检查 这些模型，并计算动力学和相互作用 模型中的组件。这些结果应该会导致更大的 对CET要求的一些结构基础的理解 B5通过细胞色素P450代谢某些底物。