Structure-Function Studies of Tight Junction Membrane Protein

紧密连接膜蛋白的结构-功能研究

• 批准号: 8516058
• 负责人: ROB Duncan COALSON
• 金额: $ 10.11万
• 依托单位: UNIVERSITY OF KANSAS MEDICAL CENTER
• 依托单位国家: 美国
• 资助国家: 美国
• 起止时间: 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/8516058
• 关键词: Apical; Berlin; Biological; Biological Assay; Biology; Boston; Cell Line; Cell Polarity; Cells; Characteristics; Charge; Collaborations; Crystallization; Disease; Electron Microscopy; Endothelium; Epithelial; Epithelial Cells; Epithelium; Extracellular Domain; Family member; Freeze Fracturing; Functional disorder; Genes; Goals; Hybrids; Integral Membrane Protein; Intestines; Ions; Kidney; Laboratories; Los Angeles; Membrane; Membrane Proteins; Methods; Modeling; Molecular; Molecular Conformation; Multigene Family; Mutagenesis; Pathway interactions; Play; Property; Protein Structure Initiative; Proteins; Research Personnel; Resolution; Role; Seminal; Skin; Structural Models; Structure; Testing; Tight Junctions; Transmembrane Domain; Work; X-Ray Crystallography; aqueous; base; interest; member; monolayer; multidisciplinary; mutant; occludin; protein expression; protein structure; protein structure function; simulation; small molecule; stoichiometry

Tight junctions have three critically important functions in both epithelia and endothelia. Tight junctions form the paracellular barrier that separates body compartments, they act as a fence that maintains apical-basolateral polarity ofthe cell, and they have paracellular pores that allow selective permeation of ions and small molecules across the cell monolayer. Three integral membrane proteins are thought to play a central role in these functions ofthe tight junction and hence are of high biological interest: claudin (a multigene family with 24 members), occludin, and tricellulin. The long-term goal of this proposal is to solve the structure of each of these proteins at atomic resolution and to use structure-guided mutagenesis to elucidate the structural mechanisms underlying their unique functions. The PI has already assembled a multidisciplinary team of investigators from Los Angeles, Pittsburgh, Boston, and Berlin to tackle the challenging problem of unraveling the function of claudins. This team has unique expertise in assaying paracellular pore function by electrophysiological methods, visualizing tight junction structure by freeze fracture electron microscopy, and hybrid molecular/Brownian dynamics modeling of pore function. The PI previously established a collaboration with the laboratory of Dr. Robert Stroud to express claudin proteins with the goal of crystallization, and has made significant progress. Thus, the applicants constitute a team that is uniquely poised to partner with a PShBiology Network Center for Membrane Protein Structure Determination to tackle the structure determination and functional characterization of tight junction membrane proteins. Aim 1. Solve the structure of claudin by X-ray crystallography Aim 2. Determine the molecular basis of the pore functions of claudin Aim 3. Determine the structural basis of the barrier and fence functions of claudin Aim 4. Structure-function comparisons of tight junction membrane proteins

紧密连接在上皮细胞和内皮细胞中都有三个至关重要的功能。紧密连接形式 分隔身体隔间的细胞旁屏障，它们起到围栏的作用 细胞的顶端-基底侧极性，它们有细胞旁的孔，允许选择性地渗透 离子和小分子穿过细胞单层。三种完整的膜蛋白被认为在 在紧密连接的这些功能中发挥中心作用，因此具有很高的生物学价值：claudin(a 有24个成员的多基因家族)、封闭蛋白和三纤维素。这项提议的长期目标是解决 在原子分辨率下分析每种蛋白质的结构，并使用结构引导突变来 阐明其独特功能背后的结构机制。 私家侦探已经组建了一个由洛杉矶、匹兹堡、 波士顿和柏林，以解决分解笨拙的功能这一具有挑战性的问题。这支球队有 在用电生理学方法分析细胞旁毛孔功能方面具有独特的专业知识，可视化紧密 用冷冻断口电子显微镜和分子/布朗混合动力学研究结结构 孔道函数的建模。PI之前与Robert博士的实验室建立了合作关系 Stroud以表达Claudin蛋白为目标，并已取得重大进展。因此， 申请者组成了一个独特的团队，准备与PShBiology Network Center合作 膜蛋白结构测定要解决的结构确定和功能 紧密连接膜蛋白的特性。 目的1.用X-射线单晶衍射法确定克拉丁的结构 目的2.确定克拉丁类药物孔功能的分子基础 目的3.确定克拉丁屏障和栅栏功能的结构基础 目的4.紧密连接膜蛋白的结构与功能比较