Theoretical Studies of Biological Charge Transfer

生物电荷转移的理论研究

• 批准号: 6473653
• 负责人: ALEXEI A STUCHEBRUKHOV
• 金额: $ 23.92万
• 依托单位: UNIVERSITY OF CALIFORNIA AT DAVIS
• 依托单位国家: 美国
• 财政年份: 1996
• 资助国家: 美国
• 起止时间: 1996-05-01 至 2006-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6473653
• 关键词: bioenergetics; charge transfer complex; chemical kinetics; computer data analysis; computer simulation; cytochrome oxidase; electron transport; enzyme complex; enzyme model; enzyme substrate; gene mutation; intermolecular interaction; intracellular transport; mathematics; membrane channels; mitochondrial membrane; model design /development; molecular dynamics; protein structure function; protonation; thermodynamics

Cytochrome oxidase (COX) is the terminal component of electron transport chain of the respiratory system in mitochondria, and one of the key enzymes responsible for energy generation in cells. COX is a proton pump. The general goal of the proposed studies is to advanced understanding of the principles and molecular mechanisms of energy transformations in this enzyme and proton pumping. In the proposed work the electron and redox coupled proton transfer reactions occurring in COX will be investigated; the computational and theoretical methods for electron and proton transfer developed in the previous grant period will be applied and further advanced. The following specific projects will be undertaken: 1)Calculation of electron transfer rates and pathways along the chain of four redox sites of the enzyme; Application, test and further advancement of the Tunneling Current Method developed in the previous grant period. Analysis of phonemenological models of ET in proteins (when and whey they are applicable to proteins). Simulation of dynamics of COX and evaluation of the dynamic effects on electron transfer. 2) Calculation of the protonation state of the enzyme as a function of its redox state for various steps along the catalytic cycle; development of in homogenous protein computational models for such calculations. Identification and studies of the effects of mutations of key protonable amino acids. 3) Studies of the redox coupled proton transfer in D- and K-channels. Simulation of water in the enzyme. Studies of the free energy rates of electron coupled proton transfer reactions. Investigation of the factors that control rates of electron and proton transfer reactions, and the overall cycle of the enzyme. 4) Development of phenomenological kinetic models of proton pumps, investigation of their efficiency, kinetic requirements, and general thermodynamic principles. These studies will contribute to molecular understanding of biological energy transformations, and will result in new computational tools for investigation of redox proteins.

细胞色素氧化酶(COX)是线粒体呼吸系统电子传递链的末端组成部分，是细胞内负责能量产生的关键酶之一。考克斯是一个质子泵。拟议研究的总体目标是促进对这种酶和质子泵中能量转换的原理和分子机制的理解。在拟议的工作中，将研究COX中发生的电子和氧化还原耦合的质子转移反应，并将应用和进一步发展前一个授权期发展的电子和质子转移的计算和理论方法。将开展以下具体项目：1)计算该酶四个氧化还原位点链上的电子转移速率和路径；应用、测试和进一步发展在前一个赠款期间开发的隧道电流法。蛋白质中ET的音系学模型分析(当它们适用于蛋白质时和乳清中)。COX动力学模拟及对电子转移的动态效应评价。2)计算酶的质子化状态作为其在催化循环中不同步骤的氧化还原状态的函数；发展用于这种计算的均相蛋白质计算模型。关键可质子化氨基酸突变效应的鉴定与研究。3)D通道和K通道中氧化还原耦合质子转移的研究。模拟水在酶中的作用。电子耦合质子转移反应自由能速率的研究。研究控制电子和质子转移反应速率的因素，以及酶的整个循环。4)发展了质子泵的唯象动力学模型，研究了它们的效率、动力学要求和一般热力学原理。这些研究将有助于分子理解生物能量转换，并将导致新的计算工具，以研究氧化还原蛋白。