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Collaborative Research: Isothermal Phase Transition in Lipid Vesicles and Swell-Burst Cycles

Collaborative Research: Isothermal Phase Transition in Lipid Vesicles and Swell-Burst Cycles
合作研究:脂质囊泡中的等温相变和膨胀-爆裂循环
批准号:
1505017
负责人:
Padmini Rangamani
金额:
$30.0万
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-05-01 至 2020-04-30

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中文摘要
翻译
在这个项目中,PI,使用理论,模拟和实验相结合,将调查脂质膜的复杂性。该项目结合了聚合物物理学、膜力学和生物工程、表面和界面科学以及软凝聚态等领域的概念,以研究生物膜的组织。建模工作将开发新的和新颖的数学和新的数值方案,以解决由此产生的微分方程。目前对多组分巨单层囊泡(GUV)如何响应渗透压差的理解是不完整的,实验观察表明,需要将膜动力学与3D流体流动耦合的非线性模型来充分解释系统的非线性。发展这一理论框架,并提供深入了解底层物理是至关重要的膜如何进行形态转变的理解。这些模型将解释现有的实验,并预测膜响应不同的渗透负荷和膜组合物。了解这一过程对于更好地设计体外重构系统(如囊泡和细胞系统)的实验非常重要。这项工作本质上是跨学科的,在生物系统中使用数学和物理学。这两个领域都将受益于这种研究生物现象的方法;该理论将以实验为基础,并对未来的实验进行预测。这项研究将被整合到PI的教学工作中,在工程和生物学的接口开发新的课程。PI将继续努力提高UC系统的多样性,同时进行研究计划。生物膜本质上是脂质和蛋白质的异质混合物。这种不均匀性的一个关键特征是液体有序相和液体无序相的共存。这种共存被认为是形成脂筏的关键组织原则。鉴于细胞的复杂性质,研究细胞系统中不同阶段的形成和组织在实验上具有挑战性。具有可控成分的巨型单层囊泡,使我们能够研究双层膜中的脂质行为,并深入了解相行为,这对于理解细胞膜非常重要。虽然GUV被广泛使用的实验,我们的脂质相分离的理论理解仍然是初步的,因为现有的模型集中在预先存在的域之间的线张力,而不是域的生长和溶胀-爆裂周期,这是实验观察到的功能。本计画的目标是建立多组份GUV中等温相分离与膨胀-爆裂循环的定量模型,并以实验验证模型的预测。研究1-溶质的结晶学。我们将使用理论,模拟和实验来了解控制孔隙半径,囊泡半径和孔隙寿命的因素。研究渗透压应力下囊泡的两相分离。使用粘弹性模型的多组分脂膜,我们将调查的作用,在域的增长与真正的相变的管理能量。我们将通过调整渗透压差、脂质成分和样品温度来实验测试模型预测。研究3-磁畴形成和膨胀-破裂循环之间的耦合。在这项研究中,我们将开发的数学框架来模拟的振荡相分离的完整动力学与溶胀-爆裂周期中观察到的初步实验。该模型将联合收割机结合研究1中概述的孔形成动力学,与研究2中包括膜粘度的域生长模型。所提出的活动的重要性在于其不仅有望阐明脂质混合物的基本性质,减少尺寸,双层构型,而且还提供了设计合成原细胞区室的设计原理,用于跨越蛋白质的体外生产,限制化学和生物医学相关货物(例如,酶、药物和显像剂)。使用理论,模拟和实验的结合,这项工作将能够提供深入了解脂质膜的复杂性。拟议活动的长期影响来自以下事实:该项目结合了聚合物物理学、膜力学和生物工程、表面和界面科学以及软凝聚物质等领域的概念。这里概述的建模工作将导致新的和新颖的数学和新的数值方案来解决由此产生的微分方程。
英文摘要
In this project the PI, using a combination of theory, simulations and experiments, will investigate the complexities of lipid membranes. The project combines concepts from the fields of polymer physics, membrane mechanics and bioengineering, surface and interface science, and soft condensed matter to study the organization of biological membranes. The modeling efforts will develop new and novel mathematics and new numerical schemes to solve the resulting differential equations. The current understanding of how multi-component giant unilamellar vesicles (GUVs) respond to osmotic pressure differentials is incomplete, and experimental observations indicate that a non-linear model coupling membrane dynamics with 3D fluid flow is needed to fully explain the non-linearities of the system. Developing this theoretical framework and providing insight into the underlying physics is crucial for the understanding of how membranes undergo morphological transitions. These models will explain existing experiments and also predict membrane response to different osmotic loads and membrane compositions. Understanding this process is important for better experimental design of in vitro reconstituted systems such as vesicles and also cellular systems. The work is inherently interdisciplinary, using mathematics and physics in biological systems. Both fields will benefit from this approach to studying biological phenomena; the theory will be grounded in experiments and also make predictions to design future experiments. This research will be integrated into the teaching efforts of the PIs in developing new courses at the interface of engineering and biology. The PIs will continue their efforts in enhancing diversity in the UC system while pursuing the research program. Biological membranes are inherently heterogeneous mixtures of lipids and proteins. A key characteristic of this heterogeneity is the coexistence of liquid-ordered and liquid-disordered phases. This coexistence is thought to be the key organizing principle for the formation of lipid rafts. Studying the formation and organization of the different phases in cellular system is experimentally challenging, given the complex nature of the cells. Giant unilamellar vesicles with controlled compositions, allow us to study lipid behavior in bilayer membranes and gain insight into phase behavior which is important for understanding cellular membranes. Although GUVs are used widely experimentally, our theoretical understanding of lipid phase separation remains rudimentary, since existing models focus on the line tension between preexisting domains and not on domain growth and swell-burst cycles, which are the features observed experimentally. The objectives of this project are to formulate quantitative models of isothermal phase separation and swell-burst cycle in multi-component GUVs and test model predictions experimentally. STUDY 1-DYNAMICS OF SOLUTE EFFLUX. We will use theory, simulations, and experiments to understand the factors that control pore radius, vesicle radius, and the lifetime of the pore. STUDY 2-PHASE SEPARATION IN OSMOTICALLY STRESSED VESICLES. Using a viscoelastic model of multi-component lipid membranes, we will investigate the role of governing energetics in domain growth versus true phase transitions. We will experimentally test the model predictions by tuning the osmotic pressure difference, lipid composition, and sample temperature. STUDY 3-COUPLING BETWEEN DOMAIN FORMATION AND SWELL-BURST CYCLES. In this study, we will develop the mathematical framework to model the complete dynamics of the oscillatory phase separation coupled with the swell-burst cycle observed in the preliminary experiments. This model will combine the dynamics of pore formation outlined in Study 1, with the domain growth model including membrane viscosity in Study 2. The significance of the proposed activities lies in its promise to not only elucidate the fundamental properties of mixtures of lipids reduced dimensional, bilayer configuration but also furnish design principles for designing synthetic protocellular compartments for applications spanning in vitro production of proteins, chemistry in confinement, and delivery of biomedically relevant cargo (e.g., enzymes, drugs, and imaging agents). Using a combination of theory, simulations and experiments, this work will be able to provide insight into the complexities of lipid membranes. The long-term impact of the proposed activities stems from the fact that the project combines concepts from the fields of polymer physics, membrane mechanics and bioengineering, surface and interface science, and soft condensed matter. The modeling efforts outlined here will result in new and novel mathematics and new numerical schemes to solve the resulting differential equations.
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Collaborative Research: MODULUS: Protein droplets drive membrane bending and cytoskeletal organization
  • 批准号:
    2327243
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $90.0万
  • 财政年份:
    2023
  • 负责人:
    Padmini Rangamani
  • 依托单位:
Collaborative Research: MODULUS: Modeling and Experimental Investigation of Protein Crowding on Lipid Bilayers
  • 批准号:
    1934411
  • 项目类别:
    Standard Grant
  • 资助金额:
    $58.87万
  • 财政年份:
    2019
  • 负责人:
    Padmini Rangamani
  • 依托单位:
Mechbio Symposium: Finding the Pieces, Building the Puzzle; University of California-San Diego; La Jolla, California; August 4-5, 2016
  • 批准号:
    1642312
  • 项目类别:
    Standard Grant
  • 资助金额:
    $1.23万
  • 财政年份:
    2016
  • 负责人:
    Padmini Rangamani
  • 依托单位:
国内基金
海外基金
Research on Quantum Field Theory without a Lagrangian Description
  • 批准号:
    24ZR1403900
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    SATOSHI NAWATA
  • 依托单位:
Cell Research
Cell Research
Cell Research (细胞研究)