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

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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.
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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.
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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

Truncation mutants define and locate cytoplasmic barriers to lateral mobility of membrane glycoproteins.

TL;DR: FPR measurements of the mobility of molecules with 7-residue domains show that length of the cytoplasmic domain has an important influence on the lateral mobility, and model calculations suggest that the barriers to lateral mobility are 2-3 nm below the membrane bilayer.
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Nonequilibrium raftlike membrane domains under continuous recycling.

TL;DR: Evidence that suggests that the average raft size may be the same for all scale-free recycling schemes, and domains can have a broad power-law distribution with an average radius that scales with the 1/4 power of the domain lifetime when the line tension at the domain edges is large.
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Noise to order

TL;DR: Some of the underlying mechanisms believed to be at the heart of crystal growth, honeycomb manufacture and floret evolution generate regular and predictable patterns are discussed.
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Differently anchored influenza hemagglutinin mutants display distinct interaction dynamics with mutual rafts

TL;DR: FRAP was employed to measure in live cells the lateral diffusion of influenza hemagglutinin (HA) proteins that differ in raft association and determined the anchoring mode determines protein–raft interaction dynamics.
Journal ArticleDOI

Imaging nanometer domains of beta-adrenergic receptor complexes on the surface of cardiac myocytes.

TL;DR: For the first time, the ability of near-field scanning optical microscopy to visualize β-adrenergic receptors at the nanoscale in situ is demonstrated and a lower limit for the number of receptors in the signalosome is established.
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