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日在意大利的Il Ciocco举行的第二届蛋白质跨细胞膜转运戈登研究会议(GRC)。这个新的会议将集中在最新的发现,提高我们对蛋白质在真核细胞,细菌和细胞器中跨膜运输或整合到膜中的机制的理解(例如,线粒体和过氧化物酶体)。由于所有细胞中超过25%的蛋白质必须穿过至少一个膜才能正确定位,因此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)用于易位的蛋白质的选择及其靶向易位位点,2)易位复合物和插入酶的结构、功能和组装,3)反向或逆转位易位,4)对易位底物折叠状态的限制,5)渗透性屏障的维持,6)膜蛋白向脂质双层的横向转移,7)脂质在蛋白质易位和膜蛋白整合中的作用,8)能量在蛋白质转运中的作用,9)蛋白质易位的调节和10)新的蛋白质易位机制。本次会议的主要目标之一是促进科学家之间的互动,他们使用不同的生物化学,遗传学,基因组学和结构方法来了解蛋白质跨膜转运的基本机制。此外,本次会议将使初级科学家接触到广泛的实验系统和问题,其中理解蛋白质易位和组装至关重要。这次会议的成立主要是为了弥补谁的工作在不同的,但概念或机制相关的蛋白质易位方面的科学家,以满足和交流思想的正式机会惊人的缺乏。在蛋白质跨细胞膜运输戈登会议的参与者将包括该领域的领导者,来自学术界,政府和工业界,以及更多的初级科学家,包括许多研究生和博士后研究员谁代表了这一领域的未来。本申请所寻求的支助的一个主要用途是协助这些年轻科学家参加会议。戈登会议的组织是为了最大限度地增加讨论和介绍该领域最新研究结果的机会,每天下午举行海报会议,每次正式会议后有讨论时间。 这次会议汇集了科学家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。本次会议将讨论与遗传性疾病有关的主题,以及细菌和病毒可能导致人类感染的方式。因此,这次会议导致对疾病原因和潜在治疗方法的了解增加。

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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