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源自脂质薄膜的巨型囊泡组装动力学

Dynamics of giant vesicle assembly from thin lipid films.

作者信息

Pazzi Joseph, Subramaniam Anand Bala

机构信息

Department of Bioengineering, University of California, Merced, CA 95343, United States.

Department of Bioengineering, University of California, Merced, CA 95343, United States.

出版信息

J Colloid Interface Sci. 2024 May;661:1033-1045. doi: 10.1016/j.jcis.2024.02.022. Epub 2024 Feb 5.

Abstract

MOTIVATION

Giant unilamellar vesicles (GUVs), cell-like synthetic micrometer size structures, assemble when thin lipid films are hydrated in aqueous solutions. Quantitative measurements of static yields and distribution of sizes of GUVs obtained from thin film hydration methods were recently reported. Dynamic data such as the time evolution of yields and distribution of sizes, however, is not known. Dynamic data can provide insights into the assembly pathway of GUVs and guidelines for choosing conditions to obtain populations with desired size distributions.

APPROACH

We develop the 'stopped-time' technique to characterize the time evolution of the distribution of sizes and molar yields of populations of free-floating GUVs. We additionally capture high resolution time-lapse images of surface-attached GUV buds on the lipid films. We systematically study the dynamics of assembly of GUVs from three widely used thin film hydration methods, PAPYRUS (Paper-Abetted amPhiphile hYdRation in aqUeous Solutions), gentle hydration, and electroformation.

FINDINGS

We find that the molar yield versus time curves of GUVs demonstrate a characteristic sigmoidal shape, with an initial yield, a transient, and then a steady state plateau for all three methods. The population of GUVs showed a right-skewed distribution of diameters. The variance of the distributions increased with time. The systems reached steady state within 120 min. We rationalize the dynamics using the thermodynamically motivated budding and merging (BNM) model. These results further the understanding of lipid dynamics and provide for the first-time practical parameters to tailor the production of GUVs of specific sizes for applications.

摘要

动机

巨型单层囊泡(GUVs)是细胞状的合成微米级结构,当脂质薄膜在水溶液中被水合时会组装形成。最近报道了从薄膜水合法获得的GUVs静态产率和尺寸分布的定量测量结果。然而,诸如产率随时间的演变以及尺寸分布等动态数据尚不清楚。动态数据可以深入了解GUVs的组装途径,并为选择条件以获得具有所需尺寸分布的群体提供指导。

方法

我们开发了“停止时间”技术来表征自由漂浮GUVs群体的尺寸分布和摩尔产率随时间的演变。我们还捕获了脂质薄膜上表面附着的GUV芽的高分辨率延时图像。我们系统地研究了三种广泛使用的薄膜水合法(PAPYRUS,即水溶液中纸辅助两亲物水合)、温和水合和电形成法中GUVs的组装动力学。

发现

我们发现GUVs的摩尔产率随时间的曲线呈现出特征性的S形,对于所有三种方法,都有一个初始产率、一个瞬态,然后是一个稳态平台期。GUVs群体的直径分布呈现右偏态。分布的方差随时间增加。这些系统在120分钟内达到稳态。我们使用热力学驱动的出芽和融合(BNM)模型来解释动力学。这些结果进一步加深了对脂质动力学的理解,并首次提供了实用参数,以定制特定尺寸GUVs的生产用于各种应用。

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