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Structure and Affinity: Computing FABP-Lipid Selectivity

结构和亲和力：计算 FABP-脂质选择性

基本信息

批准号：
7054052
负责人：
THOMAS B WOOLF
金额：
$ 26.49万
依托单位：
JOHNS HOPKINS UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2003
资助国家：
美国
起止时间：
2003-05-01 至 2007-04-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7054052
关键词：
alanine alcohols artificial intelligence chemical models fatty acid binding protein fatty acid transport fatty acids gene mutation intermolecular interaction lipid bilayer membrane molecular dynamics protein structure function site directed mutagenesis thermodynamics water

项目摘要

DESCRIPTION (provided by applicant): Physiological control of the concentration of free fatty acid levels is central to human physiology. Fatty acid binding proteins (FABPs), a large superfamily of proteins found abundantly in many cell types, have been shown to play a role in the organism's ability to control fatty acid levels by selectively binding fatty acids. The details of the ability of these proteins to select fatty acids, based on chain length, saturation state, and headgroup type, is not clear at a molecular level. This is despite the existence of two central ingredients required for such an explanation: highly detailed structures (Banaszak and Cistola) and excellent binding thermodynamics (Kleinfeld). We aim, through this grant proposal, to provide the third needed ingredient for a detailed molecular description of binding. That is, our overall goal is the ability to compute the selective binding of fatty acids within fatty acid binding proteins. We approach this goal through three specific aims. Our first aim is to understand the basis of fatty acid solvation in the homogenous solvents water and octanol. This will provide a reference point for the changes to a heterogeneous environment provided by the fatty acid binding protein and considered in the next two aims. In the second aim, we will directly compute the relative free energy differences underlying discrimination of fatty acids afforded by the intestinal fatty acid binding protein (I-FABP). In the third aim we will draw connections between our calculations and the site directed mutants that have been characterized in the Kleinfeld lab. Throughout these aims we will use alchemical mutagenesis calculations with a range of solvation models. In particular, we will be testing new models for solvation developed in the Roux lab. The work will further involve extending our own approaches to relative free energy calculations through dynamic importance sampling, analysis of non-equilibrium work events, extrapolations from histogram analysis and intelligent stepping algorithms along the alchemical reaction coordinate. If we succeed in our long term goal, we will have achieved the ability to rationally design new protein binding interactions enabling discrimination of particular fatty acids. The achievement of this goal would have implications for rational treatment of heart disease and other, e.g. digestive system related, human diseases that involve the control of free fatty acid levels.

描述（由申请人提供）：游离脂肪酸浓度水平的生理控制是人体生理学的核心。脂肪酸结合蛋白（FABPs）是在许多细胞类型中大量发现的蛋白质的大超家族，已经显示出在生物体通过选择性结合脂肪酸来控制脂肪酸水平的能力中发挥作用。这些蛋白质根据链长、饱和状态和头基类型选择脂肪酸的能力的细节在分子水平上尚不清楚。这是尽管存在的两个核心要素需要这样的解释：高度详细的结构（巴纳斯扎克和西斯托拉）和优秀的结合热力学（克莱菲尔德）。我们的目标是，通过这项拨款建议，提供第三个必要的成分，详细的分子结合的描述。也就是说，我们的总体目标是能够计算脂肪酸结合蛋白内脂肪酸的选择性结合。我们通过三个具体目标来实现这一目标。我们的第一个目标是了解脂肪酸在均相溶剂水和辛醇中溶剂化的基础。这将为脂肪酸结合蛋白提供的异质环境的变化提供参考点，并在接下来的两个目标中考虑。在第二个目标，我们将直接计算的相对自由能差异的歧视提供的脂肪酸的肠脂肪酸结合蛋白（I-FABP）。在第三个目标中，我们将在我们的计算和已经在克莱菲尔德实验室表征的定点突变体之间建立联系。在这些目标中，我们将使用炼金术诱变计算与一系列的溶剂化模型。特别是，我们将测试在Roux实验室开发的溶剂化新模型。这项工作将进一步涉及扩展我们自己的方法，通过动态重要性采样，非平衡工作事件的分析，从直方图分析和智能步进算法沿着炼金术反应坐标的外推相对自由能计算。如果我们在长期目标中取得成功，我们将实现合理设计新蛋白质结合相互作用的能力，从而能够区分特定脂肪酸。这一目标的实现将对合理治疗心脏病和其他涉及游离脂肪酸水平控制的人类疾病（例如消化系统相关疾病）具有意义。