2007 Protein Transport Across Membranes Gordon Conference

2007 年蛋白质跨膜转运戈登会议

基本信息

  • 批准号:
    7273965
  • 负责人:
  • 金额:
    $ 0.8万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2007
  • 资助国家:
    美国
  • 起止时间:
    2007-04-01 至 2008-03-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): This proposal requests support for the 2nd Protein Transport Across Cell Membranes Gordon Research Conference (GRC), to be held June 10-15, 2007 at GRC site Il Ciocco in Italy. This new meeting will focus on the latest discoveries that enhance our understanding of the mechanisms by which proteins are transported across or integrated into membranes in eukaryotic cells, bacteria and organelles (e.g., mitochondria and peroxisomes). Since >25% of all proteins in all cells must cross at least one membrane to be correctly localized, protein translocation is one of the most fundamental problems in biology. The conference will address a wide range of topics including 1) the selection of proteins for translocation and their targeting to translocation sites, 2) the structure, function and assembly of translocation complexes and insertases, 3) reverse or retro-translocation, 4) constraints on the folded state of translocation substrates, 5) the maintenance of permeability barriers, 6) lateral transfer of membrane proteins into lipid bilayers, 7) the role of lipids in protein translocation and membrane protein integration, 8) the role of energy in protein transport, 9) the regulation of protein translocation and 10) novel protein translocation mechanisms. One of the main goals of this conference is to promote interactions among scientists who use diverse biochemical, genetic, genomic and structural approaches to understand fundamental mechanisms of protein transport across membranes. In addition, this conference will expose junior scientists to a broad range of experimental systems and problems in which understanding protein translocation and assembly is critical. This conference was established primarily to compensate for a striking dearth of formal opportunities for scientists who work on different but conceptually or mechanistically related aspects of protein translocation to meet and exchange ideas. The participants at the Protein Transport Across Cell Membranes Gordon Conference will include the leaders in the field, drawn from academia, government and industry, as well as more junior scientists, including many graduate students and postdoctoral fellows who represent the future in this area. A major use of the support sought in this application is to assist such junior scientists to participate in the meeting. The Gordon Conferences are organized to maximize opportunities for discussion and for the presentation of the latest findings in the field, with poster sessions occurring every afternoon and discussion periods after each formal session. This conference brings together scientists to discuss basic mechanisms of how a cell assembles and how proteins reach their correct location. This conference will discuss topics related to inherited diseases as well as ways in with bacteria and viruses may cause infection in humans. As a result, this conference leads to an increased understanding in the cause of disease and potential therapeutic approaches.
描述(由申请人提供):本提案请求支持将于2007年6月10日至15日在意大利Il Ciocco GRC网站举行的第二届蛋白质跨膜戈登研究会议(GRC)。这次新的会议将集中于最新的发现,这些发现增强了我们对真核细胞、细菌和细胞器(例如线粒体和过氧化物体)中蛋白质跨膜运输或整合到膜上的机制的理解。由于所有细胞中25%的蛋白质必须通过至少一个膜才能正确定位,蛋白质易位是生物学中最基本的问题之一。会议将讨论广泛的主题,包括1)转位蛋白质的选择及其靶向转位位点,2)转位复合体和插入酶的结构、功能和组装,3)反向或反向转位,4)对转位底物折叠状态的限制,5)通透性屏障的维持,6)膜蛋白向脂质双层的侧向转移,7)脂类在蛋白质转位和膜蛋白整合中的作用,8)能量在蛋白质转位中的作用,9)蛋白质转位的调节和10)新的蛋白质转位机制。这次会议的主要目标之一是促进科学家之间的互动,他们使用不同的生化、遗传、基因组和结构方法来了解蛋白质跨膜运输的基本机制。此外,这次会议将使初级科学家接触到广泛的实验系统和问题,在这些系统和问题中,了解蛋白质的移位和组装是至关重要的。这次会议的设立主要是为了弥补科学家在不同但概念上或机械上相关的蛋白质转移方面工作的正式机会的惊人缺乏,以会面和交流想法。蛋白质跨细胞膜传输戈登会议的与会者将包括该领域的领导者,他们来自学术界、政府和工业界,以及更多初级科学家,包括许多代表该领域未来的研究生和博士后研究员。在这项申请中寻求的支持的一个主要用途是帮助这些初级科学家参加会议。组织戈登会议的目的是最大限度地提供讨论和介绍实地最新调查结果的机会,每天下午举行招贴会议,每次正式会议后举行讨论。 这次会议让科学家们齐聚一堂,讨论细胞如何组装以及蛋白质如何到达正确位置的基本机制。这次会议将讨论与遗传性疾病有关的话题,以及感染细菌和病毒可能导致人类感染的方法。因此,这次会议使人们对疾病的病因和潜在的治疗方法有了更多的了解。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Carla M Koehler其他文献

Carla M Koehler的其他文献

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{{ truncateString('Carla M Koehler', 18)}}的其他基金

Control of calcium flux and mitochondrial fission by the Charcot Marie Tooth disease protein Mfn2.
腓骨肌萎缩症蛋白 Mfn2 对钙通量和线粒体裂变的控制。
  • 批准号:
    10322143
  • 财政年份:
    2021
  • 资助金额:
    $ 0.8万
  • 项目类别:
Control of calcium flux and mitochondrial fission by the Charcot Marie Tooth disease protein Mfn2.
腓骨肌萎缩症蛋白 Mfn2 对钙通量和线粒体裂变的控制。
  • 批准号:
    10154169
  • 财政年份:
    2021
  • 资助金额:
    $ 0.8万
  • 项目类别:
Control of calcium flux and mitochondrial fission by the Charcot Marie Tooth disease protein Mfn2.
腓骨肌萎缩症蛋白 Mfn2 对钙通量和线粒体裂变的控制。
  • 批准号:
    10540812
  • 财政年份:
    2021
  • 资助金额:
    $ 0.8万
  • 项目类别:
Mitochondrial calcium overload and necrosis in tauopathies caused by inhibition of Mfn2 and NCLX
抑制 Mfn2 和 NCLX 引起的 tau蛋白病中线粒体钙超载和坏死
  • 批准号:
    10714837
  • 财政年份:
    2021
  • 资助金额:
    $ 0.8万
  • 项目类别:
Small Molecule Probes to Correct AGT Mistargeting in Primary Hyperoxaluria 1
用于纠正原发性高草酸尿症中 AGT 误定位的小分子探针 1
  • 批准号:
    9304851
  • 财政年份:
    2015
  • 资助金额:
    $ 0.8万
  • 项目类别:
Small Molecule Probes to Correct AGT Mistargeting in Primary Hyperoxaluria 1
用于纠正原发性高草酸尿症中 AGT 误定位的小分子探针 1
  • 批准号:
    9130819
  • 财政年份:
    2015
  • 资助金额:
    $ 0.8万
  • 项目类别:
Small Molecule Probes to Correct AGT Mistargeting in Primary Hyperoxaluria 1
用于纠正原发性高草酸尿症中 AGT 误定位的小分子探针 1
  • 批准号:
    8913596
  • 财政年份:
    2015
  • 资助金额:
    $ 0.8万
  • 项目类别:
Small molecule modulators for mitochondrial protein import
用于线粒体蛋白质输入的小分子调节剂
  • 批准号:
    7694186
  • 财政年份:
    2009
  • 资助金额:
    $ 0.8万
  • 项目类别:
Multi-user fermentation facility upgrade
多用户发酵设施升级
  • 批准号:
    7389783
  • 财政年份:
    2008
  • 资助金额:
    $ 0.8万
  • 项目类别:
RNA trafficking in mitochondria
线粒体中的RNA运输
  • 批准号:
    10461154
  • 财政年份:
    2006
  • 资助金额:
    $ 0.8万
  • 项目类别:

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