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Collaborative Research: Lanthanide Binding Tags: Biophysical Tools for Investigating Protein Structure and Function

Collaborative Research: Lanthanide Binding Tags: Biophysical Tools for Investigating Protein Structure and Function
合作研究:镧系元素结合标签:研究蛋白质结构和功能的生物物理工具
批准号:
0744483
负责人:
Barbara Imperiali
金额:
$46.96万
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-08-01 至 2012-07-31

项目摘要

项目成果

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中文摘要
翻译
知识优势:镧系结合标签(lbt)是一种小肽(15-20个残基),在它们附着的蛋白质上赋予镧系离子特异性和紧密结合。lbt允许使用依赖于结合的镧系元素的光物理性质的应用。这些序列已被整合到许多靶蛋白中,并在核磁共振、x射线晶体学和发光方面进行了应用测试。在下一阶段的研究中,LBT技术将被用于解决具有生物学意义的挑战性问题,从试管转移到细胞。新的研究将利用lbt和结合镧系元素的独特性质。也就是说,镧系元素的发光特性可以消除使用当前技术定位蛋白质和测量蛋白质运动的生物系统中复杂的高背景测量。LBT的性能将通过化学修饰来扩展,以赋予更多潜在应用的性能。该项目分为四个部分:1)lbt将用于研究蛋白质结构的动态变化,利用重要的细胞信号calcineurin A/calcineurin B复合物的发光共振能量转移特性。这些新的lbt将用于增加对细胞-细胞信号传导和细胞运输的理解。3) LBT将作为一种新型钆造影剂用于磁共振成像。4) lbt在确定蛋白质晶体结构中的应用将扩展到膜内蛋白质的溶液结构这一具有挑战性的问题。lbt将为解决这些困难的结构提供多种功能。从这些研究中获得的信息的传播将使研究界能够广泛应用lbt。在标签的开发过程中,高中生、研究生和博士后将在一个跨多学科的综合协作研究环境中接受培训。这些研究将为研究人员提供必要的基础,以解决生物,化学和物理界面上的广泛问题。研究的更广泛影响。在项目期间,lbt的使用将扩展到具有生物学重要性的应用中,为科学界提供新的lbt和定义的标签应用协议,包括蛋白质动力学研究,蛋白质信号传导和运输,细胞环境报告和整体膜蛋白结构。在标签的开发过程中,学生和博士后同事将在多个机构的分子生物学、荧光学、蛋白质化学、MRI和x射线晶体学等领域的综合协作研究环境中接受培训。这些研究将为研究人员提供必要的基础,以解决生物,化学和物理界面上的广泛问题。本科生将有机会在麻省理工学院和波士顿大学医学院的本科研究机会项目的支持下接受培训,高中生也可以通过波士顿大学城市实验室项目接受培训。麻省理工学院和波士顿大学都有积极的政策和程序,在本科和研究生阶段招募和保留代表性不足的少数民族。
英文摘要
Intellectual Merit: Lanthanide binding tags (LBTs) are small peptides (15-20 residues) that impart on the protein to which they are attached specific and tight binding of lanthanide ions. LBTs permit the use of applications that rely upon the photophysical properties of the bound lanthanides. These sequences have been integrated into many target proteins and tested for applications in nuclear magnetic resonance, X-ray crystallography, and luminescence. In the next phase of research, the LBT technology will be enlisted for addressing challenging problems of biological significance, moving from the test tube to the cell. The new studies will exploit the unique properties of the LBTs and the bound lanthanides. Namely, lanthanides luminescence properties can eliminate the high background often complicating measurements in biological systems using current technologies for locating proteins and measuring protein motion. The LBT capabilities will be extended by modification of the chemistry to impart properties with greater number of potential application. There are four parts to the project: 1) The LBTs will be used to study dynamic changes in protein structure using the property of luminescence resonance energy transfer in the important cell signaling calcineurin A/calcineurin B complex. 2) These new LBTs will be used to increase understanding of cell-cell signaling and cellular trafficking. 3) The LBT will be developed as a novel gadolinium contrast agent for use in magnetic resonance imaging. 4) The use of LBTs in determining protein crystal structures will be extended to the challenging problem of solution structure of proteins embedded in cell membranes. The LBTs will provide multiple features for the solution of these difficult structures. The dissemination of the information gained from these studies will allow the broad application of LBTs by the research communities. During the development of the tags, high school students, graduate students and postdoctoral associates will been trained in an integrated and collaborative research environment spanning multiple disciplines. These studies will provide the researchers with the foundation needed to address a broad range of problems at the interface of Biology, Chemistry and Physics. Broader Impact of the Research. During the project period, use of the LBTs will be extended in applications of biological importance, providing the scientific community with new LBTs and defined protocols for the application of the tags to a wide variety of problems including the study of protein dynamics, protein signaling and trafficking, cellular environment reporting, and the structure of integral membrane proteins. During the development of the tags, students and postdoctoral associates will be trained in an integrated and collaborative research environment spanning skill sets in molecular biology, fluorescence, protein chemistry, MRI, and X-ray crystallography at multiple institutions. These studies will provide the researchers with the foundation needed to address a broad range of problems at the interface of Biology, Chemistry and Physics. Undergraduate students will have the opportunity to be trained under the auspices of the UROP (undergraduate research opportunities) programs at MIT and Boston University School of Medicine as well as High School students through the BU CityLab program. Both MIT and Boston University have aggressive policies and procedures in action for the recruitment and retention of under-represented minorities at the undergraduate and graduate levels.
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会议论文
Collaborative Research: Development of a platform enabling analysis of membrane protein interactions
Mini-protein scaffolds for protein design
  • 批准号:
    0414243
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $64.8万
  • 财政年份:
    2004
  • 负责人:
    Barbara Imperiali
  • 依托单位:
Lanthanide Binding Tags: New Chemical Tools for Proteomics
  • 批准号:
    0304832
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $0.0万
  • 财政年份:
    2003
  • 负责人:
    Barbara Imperiali
  • 依托单位:
Design and Oligomerization of Uniquely Folded Supersecondary Structural Motifs
  • 批准号:
    0100735
  • 项目类别:
    Continuing grant
  • 资助金额:
    $0.0万
  • 财政年份:
    2001
  • 负责人:
    Barbara Imperiali
  • 依托单位:
国内基金
海外基金
Research on Quantum Field Theory without a Lagrangian Description
  • 批准号:
    24ZR1403900
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    SATOSHI NAWATA
  • 依托单位:
Cell Research
Cell Research
Cell Research (细胞研究)