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Giant Plasma Membrane Vesicles: An Experimental Tool for Probing the Effects of Drugs and Other Conditions on Membrane Domain Stability.巨型质膜囊泡:一种用于探究药物及其他条件对膜结构域稳定性影响的实验工具。
Methods Enzymol. 2018;603:129-150. doi: 10.1016/bs.mie.2018.02.007. Epub 2018 Mar 15.
2
Growth Conditions and Cell Cycle Phase Modulate Phase Transition Temperatures in RBL-2H3 Derived Plasma Membrane Vesicles.生长条件和细胞周期阶段调节源自RBL-2H3的质膜囊泡中的相变温度。
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Elucidating membrane structure and protein behavior using giant plasma membrane vesicles.使用巨大多孔脂质体阐明膜结构和蛋白质行为。
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Live cell plasma membranes do not exhibit a miscibility phase transition over a wide range of temperatures.活细胞的质膜在很宽的温度范围内不会出现混溶相变。
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本文引用的文献

1
The Effect of Solutes on the Temperature of Miscibility Transitions in Multicomponent Membranes.溶质对多组分膜中混溶转变温度的影响。
Biophys J. 2017 Oct 17;113(8):1814-1821. doi: 10.1016/j.bpj.2017.08.033.
2
n-Alcohol Length Governs Shift in L-L Mixing Temperatures in Synthetic and Cell-Derived Membranes.正醇链长度决定合成膜和细胞衍生膜中L-L混合温度的变化。
Biophys J. 2017 Sep 19;113(6):1200-1211. doi: 10.1016/j.bpj.2017.06.066. Epub 2017 Aug 9.
3
Miscibility Transition Temperature Scales with Growth Temperature in a Zebrafish Cell Line.斑马鱼细胞系中混溶转变温度随生长温度变化
Biophys J. 2017 Sep 19;113(6):1212-1222. doi: 10.1016/j.bpj.2017.04.052. Epub 2017 May 25.
4
Protein sorting by lipid phase-like domains supports emergent signaling function in B lymphocyte plasma membranes.通过类脂相结构域进行的蛋白质分选支持B淋巴细胞质膜中出现的信号功能。
Elife. 2017 Feb 1;6:e19891. doi: 10.7554/eLife.19891.
5
The Continuing Mystery of Lipid Rafts.脂筏的持续谜团。
J Mol Biol. 2016 Dec 4;428(24 Pt A):4749-4764. doi: 10.1016/j.jmb.2016.08.022. Epub 2016 Aug 26.
6
Conditions that Stabilize Membrane Domains Also Antagonize n-Alcohol Anesthesia.稳定膜结构域的条件也会拮抗正构醇麻醉。
Biophys J. 2016 Aug 9;111(3):537-545. doi: 10.1016/j.bpj.2016.06.039.
7
Polyunsaturated Lipids Regulate Membrane Domain Stability by Tuning Membrane Order.多不饱和脂质通过调节膜有序性来调控膜结构域稳定性。
Biophys J. 2016 Apr 26;110(8):1800-1810. doi: 10.1016/j.bpj.2016.03.012.
8
Membrane Protein Mobility and Orientation Preserved in Supported Bilayers Created Directly from Cell Plasma Membrane Blebs.膜蛋白流动性和取向在直接由细胞质膜泡形成的支撑双分子层中得以保留。
Langmuir. 2016 Mar 29;32(12):2963-74. doi: 10.1021/acs.langmuir.5b03415. Epub 2016 Feb 17.
9
Membrane Transition Temperature Determines Cisplatin Response.膜转变温度决定顺铂反应。
PLoS One. 2015 Oct 20;10(10):e0140925. doi: 10.1371/journal.pone.0140925. eCollection 2015.
10
Growth Conditions and Cell Cycle Phase Modulate Phase Transition Temperatures in RBL-2H3 Derived Plasma Membrane Vesicles.生长条件和细胞周期阶段调节源自RBL-2H3的质膜囊泡中的相变温度。
PLoS One. 2015 Sep 14;10(9):e0137741. doi: 10.1371/journal.pone.0137741. eCollection 2015.

巨型质膜囊泡:一种用于探究药物及其他条件对膜结构域稳定性影响的实验工具。

Giant Plasma Membrane Vesicles: An Experimental Tool for Probing the Effects of Drugs and Other Conditions on Membrane Domain Stability.

作者信息

Gerstle Zoe, Desai Rohan, Veatch Sarah L

机构信息

University of Michigan, Ann Arbor, MI, United States.

University of Michigan, Ann Arbor, MI, United States.

出版信息

Methods Enzymol. 2018;603:129-150. doi: 10.1016/bs.mie.2018.02.007. Epub 2018 Mar 15.

DOI:10.1016/bs.mie.2018.02.007
PMID:29673522
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6070695/
Abstract

Giant plasma membrane vesicles (GPMVs) are isolated directly from living cells and provide an alternative to vesicles constructed of synthetic or purified lipids as an experimental model system for use in a wide range of assays. GPMVs capture much of the compositional protein and lipid complexity of intact cell plasma membranes, are filled with cytoplasm, and are free from contamination with membranes from internal organelles. GPMVs often exhibit a miscibility transition below the growth temperature of their parent cells. GPMVs labeled with a fluorescent protein or lipid analog appear uniform on the micron-scale when imaged above the miscibility transition temperature, and separate into coexisting liquid domains with differing membrane compositions and physical properties below this temperature. The presence of this miscibility transition in isolated GPMVs suggests that a similar phase-like heterogeneity occurs in intact plasma membranes under growth conditions, albeit on smaller length scales. In this context, GPMVs provide a simple and controlled experimental system to explore how drugs and other environmental conditions alter the composition and stability of phase-like domains in intact cell membranes. This chapter describes methods to generate and isolate GPMVs from adherent mammalian cells and to interrogate their miscibility transition temperatures using fluorescence microscopy.

摘要

巨质膜囊泡(GPMVs)直接从活细胞中分离得到,为在各种检测中用作实验模型系统的由合成或纯化脂质构建的囊泡提供了一种替代方案。GPMVs保留了完整细胞质膜在组成上的蛋白质和脂质复杂性,内部充满细胞质,且不受来自内部细胞器膜的污染。GPMVs在其亲本细胞的生长温度以下常常表现出混溶转变。当在混溶转变温度以上成像时,用荧光蛋白或脂质类似物标记的GPMVs在微米尺度上看起来是均匀的,而在该温度以下会分离成具有不同膜组成和物理性质的共存液相区域。分离得到的GPMVs中这种混溶转变的存在表明,在生长条件下完整质膜中会发生类似的相状异质性,尽管其长度尺度更小。在这种情况下,GPMVs提供了一个简单且可控的实验系统,用于探究药物和其他环境条件如何改变完整细胞膜中相状区域的组成和稳定性。本章描述了从贴壁哺乳动物细胞中生成和分离GPMVs以及使用荧光显微镜测定其混溶转变温度的方法。