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Open AccessJournal ArticleDOI

Dynamics in the plasma membrane: how to combine fluidity and order

TLDR
The basic concepts of Brownian diffusion and lipid domain formation in model membranes are summarized and the development of ideas and tools in this field are tracked, outlining key results obtained on the dynamic processes at work in membrane structure and assembly.
Abstract
Cell membranes are fascinating supramolecular aggregates that not only form a barrier between compartments but also harbor many chemical reactions essential to the existence and functioning of a cell. Here, it is proposed to review the molecular dynamics and mosaic organization of the plasma membrane, which are thought to have important functional implications. We will first summarize the basic concepts of Brownian diffusion and lipid domain formation in model membranes and then track the development of ideas and tools in this field, outlining key results obtained on the dynamic processes at work in membrane structure and assembly. We will focus in particular on findings made using fluorescent labeling and imaging procedures to record these dynamic processes. We will also discuss a few examples showing the impact of lateral diffusion on cell signal transduction, and outline some future methodological challenges which must be met before we can answer some of the questions arising in this field of research.

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Journal ArticleDOI

Lipid rafts: at a crossroad between cell biology and physics.

TL;DR: The concept of lipid rafts as it has emerged from the study of synthetic membranes with the reality of lateral heterogeneity in biological membranes is compared.
Journal ArticleDOI

Coordination of Rho GTPase activities during cell protrusion

TL;DR: GTPase coordination in mouse embryonic fibroblasts is examined both through simultaneous visualization of two GTPase biosensors and using a ‘computational multiplexing’ approach capable of defining the relationships between multiple protein activities visualized in separate experiments, finding that RhoA is activated at the cell edge synchronous with edge advancement, whereas Cdc42 and Rac1 are activated 2 μm behind the edge with a delay of 40 s.
Journal ArticleDOI

Dynamic multiple-target tracing to probe spatiotemporal cartography of cell membranes.

TL;DR: An analytical single-particle tracking method and tool, multiple-target tracing (MTT), that takes advantage of the high spatial resolution provided by single-fluorophore sensitivity to generate dynamic maps at high densities of tracked particles, thereby providing global representation of molecular dynamics in cell membranes.
Journal ArticleDOI

Organization and Ca2+ Regulation of Adenylyl Cyclases in cAMP Microdomains

TL;DR: The regulation of many of the ACs by the ubiquitous second messenger Ca(2+) provides an overarching mechanism for integrating the activities of these two major signaling systems, and cAMP will exhibit distinct kinetics in discrete cellular domains.
References
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Journal ArticleDOI

Membranes are more mosaic than fluid

TL;DR: The wealth of new data on membrane protein structures and functions is changing the general view of membrane architecture, and some of the key themes that are emerging are that membranes are patchy, with segregated regions of structure and function, that lipid regions vary in thickness and composition.
Journal ArticleDOI

Characterization of lipid bilayer phases by confocal microscopy and fluorescence correlation spectroscopy

TL;DR: Three-dimensional image reconstructions of confocal z-scans through giant unilamellar vesicles reveal the anisotropic morphology of coexisting phase domains on the surface of these vesicle with full two-dimensional resolution, answering a long-standing open question.
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Breaking the diffraction barrier in fluorescence microscopy at low light intensities by using reversibly photoswitchable proteins

TL;DR: The surpassing of the diffraction barrier in fluorescence microscopy with illumination intensities that are eight orders of magnitude smaller is demonstrated, underscoring the potential to finally achieve molecular resolution in fluorescent microscopy by technical optimization.
Journal ArticleDOI

The rapid intermixing of cell surface antigens after formation of mouse-human heterokaryons.

TL;DR: It appears that the cell surface of heterokaryons is not a rigid structure, but is ‘fluid’ enough to allow free ‘diffusion’ of surface antigens resulting in their intermingling within minutes after the initiation of fusion.
Journal ArticleDOI

Single-molecule microscopy reveals plasma membrane microdomains created by protein-protein networks that exclude or trap signaling molecules in T cells.

TL;DR: It is shown that the coreceptor CD2, the adaptor protein LAT, and tyrosine kinase Lck cocluster in discrete microdomains in the plasma membrane of signaling T cells, which require protein-protein interactions mediated through phosphorylation of LAT and are not maintained by interactions with actin or lipid rafts.
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