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中文摘要
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描述(由申请人提供):膜转运蛋白是细胞膜上活性物质交换的主要参与者,是活细胞中最基本和高度调控的过程之一。因此,研究其功能的分子基础在生物学和生物医学研究的各个学科中至关重要。这些复杂的蛋白质提供了高度复杂、操作精细的分子机器,有效地将细胞中的各种能量来源与各种分子物种在膜上的矢量易位结合起来,以对抗其化学梯度。研究膜转运蛋白的分子机制是一项重大挑战,主要是由于它们的结构复杂性和由它们提供的能量依赖运输过程的高维性。在膜转运体中,底物结合和沿渗透途径的易位与许多不同程度的蛋白质构象变化密切相关,这些变化是由能量提供机制诱导和/或协调的,例如质子和其他离子的结合和共运输,或ATP的结合和水解。因此,对膜转运体中转运机制的详细描述依赖于能够在原子水平上描述这些过程的动力学的方法。分子动力学模拟仍然是一种高度相关的方法,具有足够的时间和空间分辨率来研究这些过程。将该方法应用于膜转运体是一个非常年轻的研究领域,因为这种模拟所需的足够的结构数据直到最近才可用。此外,为了描述膜转运蛋白功能中涉及的生物学相关事件和步骤,需要对这些大分子进行至少0.1-1 <s数量级的原子模拟,这一计算需求直到最近才得到满足。尽管仍然极具挑战性,但由于膜转运蛋白结构发现的及时收敛以及计算机硬件和软件的进步,我们现在处于前所未有的位置,可以将模拟研究的范围扩展到膜转运蛋白领域并研究其功能的分子基础。在这项申请中,我们提出了研究三种活性膜转运蛋白的项目:(1)麦芽糖转运蛋白,一种ABC转运蛋白,其中ATP结合和水解驱动底物运输过程;(2)谷氨酸转运体(Glutamate transporter, GluT),代表二级转运体,利用跨膜的离子梯度作为其功能的能量来源;(3)线粒体ADP/ATP载体(AAC),它依靠膜电位在细胞质和线粒体之间交换核苷酸。与公共卫生相关:膜转运蛋白是介导多种物质(如营养物质、激素和神经递质)跨细胞膜选择性转运的蛋白质。它们对人体生理学的几乎所有方面都是必不可少的,它们的功能障碍与许多人类疾病有关。本应用程序的研究将在分子水平上研究几种膜转运蛋白的功能机制。
英文摘要
DESCRIPTION (provided by applicant): Membrane transporters are principal players in active exchange of materials across the cellular membrane, one of the most fundamental and highly regulated processes in living cells. Investigating the molecular basis of their function, therefore, is of utmost importance in various disciplines of biological and biomedical research. These complex proteins provide highly sophisticated, operationally fine-tuned molecular machines to efficiently couple various sources of energy in the cell to vectorial translocation of various molecular species across the membrane against their chemical gradient. Investigation of the molecular details of the mechanism of membrane transporters poses a major challenge, primarily due to their structural complexity and the high dimensionality of the process of energy-dependent transport furnished by them. Substrate binding and translocation along the permeation pathway in membrane transporters is closely coupled to numerous stepwise protein conformational changes of various magnitudes that are induced and/or coordinated by the energy- providing mechanisms, e.g., binding and co-transport of protons and other ions, or binding and hydrolysis of ATP. A detailed description of the mechanism of transport in membrane transporters, therefore, relies on methods that can describe the dynamics of these processes at an atomic level. Molecular dynamics simulation remains a highly relevant approach with sufficient temporal and spatial resolutions to investigate such processes. Application of the method to membrane transporters is a very young area of research, since sufficient structural data required for such simulations has become available only recently. Furthermore, in order to describe biologically relevant events and steps involved in the function of membrane transporters, atomistic simulations of these large biomolecules on the orders of at least 0.1-1 <s are required, a computational demand which has also been met only recently. Though still extremely challenging, owing to the timely convergence of discoveries of membrane transporter structures and advances in computer hardware and software, we are now in an unprecedented position to expand the scope of simulation studies into the realm of membrane transporters and investigate the molecular basis of their function. In this application, we propose projects investigating three active membrane transporters: (1) Maltose transporter, an ABC transporter in which ATP binding and hydrolysis drive the process of substrate transport; (2) Glutamate transporter (GluT), representing secondary transporters that use the ionic gradient across the membrane as the source of energy for their function; and (3) the mitochondrial ADP/ATP carrier (AAC) which relies on the membrane potential for exchange of nucleotides betwee the cytoplasm and the mitochondria. PUBLIC HEALTH RELEVANCE: Membrane transporters are proteins that mediate selective transport of a wide range of materials, e.g., nutrients, hormones, and neurotransmitters, across the cellular membrane. They are essential to almost all aspects of human physiology, and their malfunction is associated with a large number of human diseases. The research proposed in this application will investigate the mechanism of function of several membrane transporters at a molecular level.
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DOI: 10.1529/biophysj.108.139444
发表时间: 2008-12
期刊: Biophysical journal
影响因子: 3.4
作者: [Po-Chao Wen;E. Tajkhorshid]
通讯作者: Po-Chao Wen;E. Tajkhorshid
Resource for Macromolecular Modeling and Visualization
Administrative Supplement: Resource for Macromolecular Modeling and Visualization
Resource for Macromolecular Modeling and Visualization
Hands-on Workshops on Computational Biophysics
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