课题基金 / 基金详情

项目摘要

项目成果

THOMAS WALZ的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
The EM core of this Program Project has two related purposes - to support instrumentation essential for the research proposed in the four projects of this grant and to facilitate application of the methods being developed in these projects to collaborative and independent efforts. The principal components of the core are the electron microscopy facilities at Harvard Medical School (HMS) and at Brandeis University. The HMS facility will house four FBI microscopes: a Tecnai F20, a Tecnai T12, a CM10, and a Polara F30. The F30, the F20, and the T12 microscopes are equipped with cryo-stages; the F30 and the F20 have field-emission guns. The Brandeis facility also houses four FBI instruments: a Morgagni M268, and EM20, a CM12, and a Tecnai F30. The last three have cryo-stages; the F30 has a field-emission gun and an energy filter. The core supports the operation of these microscopes and the salary of a facilities manager at each location, as well as necessary ancillary equipment. The core also has a computational component. It maintainsand upgrades all standard EM software, including program suites such as FREALIGN, IMAGIC, and SPIDER, through a structural biology computational grid (SBGrid) established by the Center for Molecular and Cellular Dynamics at HMS. Finally, by providing EM and computational facilities, the core allows the P.I.'s of these projects to collaborate with other groups at various institutionsand to train postdoctoral fellows and students in the relevant methods. Relevance: Electron microscopy is the key experimental tool that bridges between low- and high-resolution structural methods. Large assemblies will be targets of future interventions in human disease, and electron microscopy will be central for relating structure and function of these complexes
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Elucidating the gating mechanisms of bacterial mechanosensitive channels
  • 批准号:
    10583324
  • 项目类别:
  • 资助金额:
    $49.01万
  • 财政年份:
    2023
  • 负责人:
    THOMAS WALZ
  • 依托单位:
Elucidating the gating mechanisms of bacterial mechanosensitive channels
  • 批准号:
    10796256
  • 项目类别:
  • 资助金额:
    $10.74万
  • 财政年份:
    2023
  • 负责人:
    THOMAS WALZ
  • 依托单位:
Project 2: Walz
  • 批准号:
    8462409
  • 项目类别:
  • 资助金额:
    $24.76万
  • 财政年份:
    2012
  • 负责人:
    THOMAS WALZ
  • 依托单位:
Structural and functional studies of urea channels
  • 批准号:
    8019537
  • 项目类别:
  • 资助金额:
    $21.55万
  • 财政年份:
    2008
  • 负责人:
    THOMAS WALZ
  • 依托单位:
国内基金
海外基金
通过Clathrin/AP2途径介导内皮细胞Occludin自噬性降解以靶向开放胶质瘤血肿瘤屏障的机制研究
  • 批准号:
    --
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    30万元
  • 批准年份:
    2022
  • 负责人:
    艾潇琳
  • 依托单位:
GRB2/Clathrin/ESCRT介导的内吞、运输及溶酶体降解在CD7 CAR-T细胞诱导T细胞CD7阴性表达的机制研究
  • 批准号:
    82270234
  • 项目类别:
    面上项目
  • 资助金额:
    52万元
  • 批准年份:
    2022
  • 负责人:
    胡永仙
  • 依托单位:
TMEM30A通过Clathrin介导的囊泡转运参与足细胞损伤的机制研究
  • 批准号:
    --
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    30万元
  • 批准年份:
    2022
  • 负责人:
    彭雷
  • 依托单位:
活细胞高分辨率成像解析clathrin介导的内吞囊泡形成早期内体的分子机制