Literature DB >> 29673522

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

Zoe Gerstle1, Rohan Desai1, Sarah L Veatch2.   

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.
© 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Lipid raft; Liquid-disordered; Liquid-ordered; Miscibility; Phase transition; Plasma membrane; Vesicle

Mesh:

Substances:

Year:  2018        PMID: 29673522      PMCID: PMC6070695          DOI: 10.1016/bs.mie.2018.02.007

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  62 in total

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3.  Liquid general anesthetics lower critical temperatures in plasma membrane vesicles.

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4.  Conditions that Stabilize Membrane Domains Also Antagonize n-Alcohol Anesthesia.

Authors:  Benjamin B Machta; Ellyn Gray; Mariam Nouri; Nicola L C McCarthy; Erin M Gray; Ann L Miller; Nicholas J Brooks; Sarah L Veatch
Journal:  Biophys J       Date:  2016-08-09       Impact factor: 4.033

5.  Line tensions, correlation lengths, and critical exponents in lipid membranes near critical points.

Authors:  Aurelia R Honerkamp-Smith; Pietro Cicuta; Marcus D Collins; Sarah L Veatch; Marcel den Nijs; M Schick; Sarah L Keller
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6.  The effect of anaesthetics on the dynamic heterogeneity of lipid membranes.

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Journal:  Chem Phys Lipids       Date:  1993-10       Impact factor: 3.329

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Authors:  Sarah L Veatch; Sarah L Keller
Journal:  Biophys J       Date:  2003-11       Impact factor: 4.033

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Review 9.  Mechanisms of general anesthesia.

Authors:  N P Franks; W R Lieb
Journal:  Environ Health Perspect       Date:  1990-07       Impact factor: 9.031

10.  n-Alcohol Length Governs Shift in Lo-Ld Mixing Temperatures in Synthetic and Cell-Derived Membranes.

Authors:  Caitlin E Cornell; Nicola L C McCarthy; Kandice R Levental; Ilya Levental; Nicholas J Brooks; Sarah L Keller
Journal:  Biophys J       Date:  2017-08-09       Impact factor: 4.033

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  8 in total

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4.  Compartmentalization of phosphatidylinositol 4,5-bisphosphate metabolism into plasma membrane liquid-ordered/raft domains.

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6.  Lateral heterogeneity and domain formation in cellular membranes.

Authors:  Jacob J Kinnun; Dima Bolmatov; Maxim O Lavrentovich; John Katsaras
Journal:  Chem Phys Lipids       Date:  2020-09-15       Impact factor: 3.329

7.  Fluorescence Microscopy-Based Quantitation of GLUT4 Translocation: High Throughput or High Content?

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8.  Degranulation enhances presynaptic membrane packing, which protects NK cells from perforin-mediated autolysis.

Authors:  Yu Li; Jordan S Orange
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  8 in total

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