课题基金 / 基金详情

Mechanisms of Interleaflet Coupling in Asymmetric Lipid Membranes

Mechanisms of Interleaflet Coupling in Asymmetric Lipid Membranes
不对称脂质膜中的叶间偶联机制
批准号:
1817929
负责人:
Frederick Heberle
金额:
$74.96万
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-07-01 至 2023-06-30

项目摘要

项目成果

Frederick Heberle的其他基金

相关文献

中文摘要
翻译
活细胞通过一层薄薄的双层脂质和相关蛋白质(称为质膜)与外界交流。这种膜的一个显著特征是它的两半在化学上是不同的:面向细胞内部内容物的脂质与面向外部环境的脂质非常不同。目前尚不清楚这种成分不对称性在健康细胞的生命中起着什么作用,但很明显,没有它,细胞就无法正常工作,事实上,它们消耗了宝贵的能量来积极维持它。本项目旨在通过回答细胞膜的两半如何相互沟通和影响的基本问题,揭示细胞膜不对称性的奥秘。这将通过系统研究在不对称膜的每一侧发现的不同类型的脂质如何影响另一半的性质以及整个膜的性质来实现。由于膜的大部分功能来自其宿主的蛋白质,研究人员还将研究膜驻留蛋白质如何影响,进而受到脂质不对称性的影响。在这个项目的过程中,主要研究人员将培训研究生和博士后研究人员的实验和计算方法,这将为他们在STEM领域的职业生涯做好准备。研究人员将通过会议报告和同行评议的出版物将他们的发现传达给科学界,还将通过外展计划吸引公众参与,以提高对生物物理研究的认识和赞赏。两个双层小叶的成分不对称是大多数细胞膜的基本属性,包括包围细胞的质膜。虽然这种不对称性对细胞活力至关重要,但其在正常细胞功能中的作用知之甚少。该项目将阐明管理不对称模型膜的两个半之间的通信的规则,从而改善基于膜的不对称脂质组成的功能表型的预测。该项目的主要目标是使用中子散射技术来揭示每个小叶的结构和动力学特性如何响应脂质组成的变化,并将实验结果与原子模拟相结合,以了解导致这些变化的潜在分子机制。第二个目标是更深入地了解不对称膜如何适应跨膜蛋白的存在,以及蛋白质如何反过来响应不对称脂质环境。虽然脂质提供了生物膜的基本结构,蛋白质提供了大部分的功能;这个项目将提供急需的信息,蛋白质-脂质相互作用的生物相关的背景下,不对称膜。第三个目标是继续开发用于制备和表征复杂非对称囊泡的稳健技术,以用作先进的质膜模型systems.This奖项反映了NSF的法定使命,并已被视为值得通过使用基金会的智力价值和更广泛的影响审查标准进行评估的支持。
英文摘要
Living cells communicate with the outside world through a thin double layer of lipids and associated proteins called the plasma membrane. A remarkable feature of this membrane is that its two halves are chemically distinct: the lipids that face the internal contents of the cell are very different from the lipids that face the external environment. It is not clear what role this compositional asymmetry plays in the life of a healthy cell, yet it is clear that cells do not function properly without it, and indeed they expend valuable energy to actively maintain it. This project aims to shed light on the mystery of cell membrane asymmetry by answering the basic question of how the two halves of a membrane communicate with and influence each other. This will be accomplished through the systematic study of how the different types of lipids that are found on each side of an asymmetric membrane influence the properties of the other half, as well as the properties of the membrane as a whole. Because much of a membrane's functionality is derived from the proteins it hosts, the researchers will also investigate how a membrane-resident protein affects, and is in turn affected by lipid asymmetry. In the course of this project, the principle investigator will train graduate students and postdoctoral researchers in experimental and computational methods that will prepare them for careers in STEM fields. The researchers will communicate their findings to the scientific community through conference presentations and peer-reviewed publications and will also engage the public through an outreach program to enhance awareness of and appreciation for biophysical research.Compositional asymmetry of the two bilayer leaflets is a fundamental property of most cellular membranes, including the plasma membrane that surrounds the cell. Although this asymmetry is essential for cell viability, its role in normal cellular function is poorly understood. This project will elucidate the rules that govern communication between the two halves of asymmetric model membranes, leading to improved predictions of functional phenotypes based on the asymmetric lipid composition of a membrane. A primary goal of the project is the use of neutron scattering techniques to reveal how the structural and dynamical properties of each leaflet respond to changes in lipid composition, and to integrate the experimental results with atomistic simulations to inform on the underlying molecular mechanisms responsible for these changes. A second objective is to develop a deeper understanding of how asymmetric membranes adapt to the presence of a transmembrane protein, and how the protein responds in turn to an asymmetric lipid environment. While lipids provide the basic structure of biomembranes, proteins provide most of the functionality; this project will provide much needed information about protein-lipid interactions in the biologically relevant context of an asymmetric membrane. A third objective is the continued development of robust techniques for preparing and characterizing complex asymmetric vesicles for use as advanced plasma membrane model systems.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.
期刊论文(25)
专著(0)
科研奖励(0)
会议论文
Visualizing lipid membrane structure with cryo-EM: past, present, and future
使用冷冻电镜可视化脂质膜结构:过去、现在和未来
DOI: 10.1042/etls20220090
发表时间: 2023
期刊: Emerging Topics in Life Sciences
影响因子: 3.8
作者: [Sharma, Karan D., Heberle, Frederick A., Waxham, M. Neal]
通讯作者: Waxham, M. Neal
DOI: 10.1021/acs.langmuir.9b01625
发表时间: 2019-09-10
期刊: LANGMUIR
影响因子: 3.9
作者: [Nguyen, Michael H. L., DiPasquale, Mitchell, Marquardt, Drew]
通讯作者: Marquardt, Drew
DOI: 10.1016/j.chemphyslip.2022.105205
发表时间: 2022-07
期刊: CHEMISTRY AND PHYSICS OF LIPIDS
影响因子: 3.4
作者: [DiPasquale, Mitchell, Deering, Tye G., Desai, Dhimant, Sharma, Arun K., Amin, Shantu, Fox, Todd E., Kester, Mark, Katsaras, John, Marquardt, Drew, Heberle, Frederick A.]
通讯作者: Heberle, Frederick A.
DOI: 10.3390/membranes13070629
发表时间: 2023-06-29
期刊: Membranes
影响因子: 4.2
作者: []
通讯作者:
共 15 条
    Development of cryogenic electron microscopy for probing phase separation in lipid membranes
    • 批准号:
      2204126
    • 项目类别:
      Standard Grant
    • 资助金额:
      $68.42万
    • 财政年份:
      2022
    • 负责人:
      Frederick Heberle
    • 依托单位: