PROBING PHOSPHORYLATION EVENTS IN BIOLOGICAL MEMBRANES

探测生物膜中的磷酸化事件

基本信息

  • 批准号:
    2106031
  • 负责人:
  • 金额:
    $ 100.49万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
    Standard Grant
  • 财政年份:
    2021
  • 资助国家:
    美国
  • 起止时间:
    2021-07-01 至 2025-06-30
  • 项目状态:
    未结题

项目摘要

The plasma membrane, which surrounds every cell, must not only permit selective uptake of nutrients, but also allow for information to be communicated across it so that the cell can appropriately respond to external signals. A family of membrane-embedded proteins that transduces signals across the plasma membrane, known as receptor tyrosine kinases (RTK), stimulates diverse processes such as the growth of blood vessels or the response to insulin. Intriguingly, individual RTKs can respond to multiple signals, and the biological consequences of the response can differ. How a single RTK can trigger distinct downstream processes in response to different stimuli is unknown. The goal of the project is to establish a method that quantifies the very first step in the information transfer pathway to define the efficiency of signal transduction across the plasma membrane. Differences in the efficiencies with which the various stimuli signal through an RTK may explain the distinct processes triggered by the stimuli. The project will provide research opportunities for graduate students and will enhance the educational experience of undergraduate students who are conducting research. In addition, it will support broad outreach activities benefiting young scientists from diverse backgrounds and students in Baltimore.The first objective of the project is to establish osmotically-derived plasma membrane vesicles as a model system for RTK phosphorylation transducer function measurements in fluorescence microscopy experiments. The second objective is to measure the transducer function for epidermal growth factor (EGFR) phosphorylation in response to its activating ligands. The third objective is to measure the transducer function for fibroblast growth factor receptor 3 (FGFR3) phosphorylation in response to its ligands. The ultimate goal is to directly compare the transducer functions for different RTK-ligand pairs and thus gain insights into the differential functional effects mediated by the different ligands. The new methodology will strengthen the over-all experimental capabilities in the field of molecular membrane biophysics. In the long run, the methodology can also be used to advance knowledge about different types of receptors such as (i) cytokine receptors and associated Janus kinases, which modulate antiviral and anti-cancer activities and inflammatory responses, (ii) death receptors, which initiate cytotoxic signals upon ligand binding, and (iii) G-protein coupled receptors, which mediate the recognition of light, taste, odors, hormones, pain, and neurotransmitters.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
围绕着每个细胞的质膜不仅允许选择性地吸收营养物质,而且还允许信息通过它进行交流,以便细胞能够对外部信号做出适当的反应。 一个跨质膜转导信号的膜包埋蛋白家族,称为受体酪氨酸激酶(RTK),刺激不同的过程,如血管生长或对胰岛素的反应。 有趣的是,单个RTK可以响应多种信号,并且响应的生物后果可能不同。 单个RTK如何能够响应于不同的刺激而触发不同的下游过程是未知的。该项目的目标是建立一种方法,量化信息传递途径中的第一步,以确定跨质膜信号转导的效率。 各种刺激信号通过RTK的效率差异可以解释由刺激触发的不同过程。该项目将为研究生提供研究机会,并将加强正在进行研究的本科生的教育经验。此外,它将支持广泛的推广活动,受益于来自不同背景的年轻科学家和学生在巴尔的摩。该项目的第一个目标是建立一个模型系统的RTK磷酸化转换器功能测量荧光显微镜实验中的质膜囊泡。第二个目标是测量表皮生长因子(EGFR)磷酸化的换能器功能,以响应其活化配体。 第三个目的是测量成纤维细胞生长因子受体3(FGFR 3)磷酸化对其配体的应答的转换器功能。 最终目标是直接比较不同RTK-配体对的换能器功能,从而深入了解不同配体介导的差异功能效应。新的方法将加强在分子膜生物物理学领域的整体实验能力。从长远来看,该方法也可用于推进关于不同类型受体的知识,例如(i)细胞因子受体和相关的Janus激酶,其调节抗病毒和抗癌活性以及炎症反应,(ii)死亡受体,其在配体结合时引发细胞毒性信号,和(iii)G蛋白偶联受体,其介导光、味觉、气味、激素、疼痛、该奖项反映了NSF的法定使命,并通过使用基金会的知识价值和更广泛的影响审查标准进行评估,被认为值得支持。

项目成果

期刊论文数量(1)
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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Kalina Hristova其他文献

A Phosphorylation-Based Model for EGFR Activation as a Function of Ligand Concentration
  • DOI:
    10.1016/j.bpj.2008.12.1654
  • 发表时间:
    2009-02-01
  • 期刊:
  • 影响因子:
  • 作者:
    Edwin Li;Jesse K. Placone;Kalina Hristova
  • 通讯作者:
    Kalina Hristova
The L920F EphA4 Oncogenic Mutation Alters the SAM Domain Fold and Induces EphA4 Oligomerization
  • DOI:
    10.1016/j.bpj.2020.11.2075
  • 发表时间:
    2021-02-12
  • 期刊:
  • 影响因子:
  • 作者:
    Taylor P. Light;Zichen Wang;Kelly Karl;Elmer A. Zapata-Mercado;Taras V. Pogorelov;Jeffrey J. Gray;Kalina Hristova
  • 通讯作者:
    Kalina Hristova
Investigating the Association of Ephrin Type-B Receptor Tyrosine Kinases in Live Cells
  • DOI:
    10.1016/j.bpj.2017.11.2549
  • 发表时间:
    2018-02-02
  • 期刊:
  • 影响因子:
  • 作者:
    Taylor Patrick Light;Kalina Hristova
  • 通讯作者:
    Kalina Hristova
The Isolated S4 Voltage Sensor Helix Translocates Spontaneously Across Membranes
  • DOI:
    10.1016/j.bpj.2011.11.3354
  • 发表时间:
    2012-01-31
  • 期刊:
  • 影响因子:
  • 作者:
    William C. Wimley;Kalina Hristova
  • 通讯作者:
    Kalina Hristova
Effect of Melittin and Gain-of-Function Melittin Analogs, Discovered by High-Throughput Screening, on Bilayer Properties: An Electrical Impedance Spectroscopy Study
  • DOI:
    10.1016/j.bpj.2011.11.517
  • 发表时间:
    2012-01-31
  • 期刊:
  • 影响因子:
  • 作者:
    Gregory Wiedman;William Wimley;Peter Searson;Kalina Hristova
  • 通讯作者:
    Kalina Hristova

Kalina Hristova的其他文献

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{{ truncateString('Kalina Hristova', 18)}}的其他基金

Collaborative Research: Lipid Bilayers and Membrane Active Peptides
合作研究:脂质双层和膜活性肽
  • 批准号:
    1709892
  • 财政年份:
    2017
  • 资助金额:
    $ 100.49万
  • 项目类别:
    Standard Grant
Biophysics of protein interactions on membrane surfaces
膜表面蛋白质相互作用的生物物理学
  • 批准号:
    1712740
  • 财政年份:
    2017
  • 资助金额:
    $ 100.49万
  • 项目类别:
    Standard Grant
Lateral interactions between proteins in membranes
膜中蛋白质之间的横向相互作用
  • 批准号:
    1157687
  • 财政年份:
    2012
  • 资助金额:
    $ 100.49万
  • 项目类别:
    Continuing Grant
Collaborative Research: Lipid Bilayers and Interfacially Active Peptides
合作研究:脂质双层和界面活性肽
  • 批准号:
    1003441
  • 财政年份:
    2010
  • 资助金额:
    $ 100.49万
  • 项目类别:
    Continuing Grant
Probing the Dimerization of Transmembrane Helices in Eukaryotic and Lipid Bilayer Membranes
探讨真核生物和脂质双层膜中跨膜螺旋的二聚化
  • 批准号:
    0718841
  • 财政年份:
    2007
  • 资助金额:
    $ 100.49万
  • 项目类别:
    Continuing Grant
Probing the Dimerization of Transmembrane Helices in Lipid Bilayers
探讨脂质双层中跨膜螺旋的二聚化
  • 批准号:
    0315663
  • 财政年份:
    2003
  • 资助金额:
    $ 100.49万
  • 项目类别:
    Continuing Grant

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DNA 损伤修复中磷酸化介导的信号事件的时间解析
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