Literature DB >> 19840867

A novel form of Total Internal Reflection Fluorescence Microscopy (LG-TIRFM) reveals different and independent lipid raft domains in living cells.

Alexander Asanov1, Angélica Zepeda, Luis Vaca.   

Abstract

In the present study we have applied a novel form of Total Internal Reflection Fluorescence Microscopy (LG-TIRFM) in combination with fluorescently labeled cholera toxin to the study of lipid rafts dynamics in living cells. We demonstrate the usefulness of such approach by showing the dynamic formation/disaggregation of islands of cholera toxin on the surface of cells. Using multicolor LG-TIRFM with co-localization studies we show for the first time that two receptors previously identified as constituents of lipid rafts are found on different and independent "raft domains" on the cell plasma membrane. Furthermore, LG-TIRFM studies revealed limited association and dissociation of both domains overtime on different areas of the plasma membrane. The implications of different "raft domains" on cell physiology are discussed. 2009 Elsevier B.V. All rights reserved.

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Year:  2009        PMID: 19840867     DOI: 10.1016/j.bbalip.2009.10.004

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  16 in total

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Review 4.  Recent progress on lipid lateral heterogeneity in plasma membranes: From rafts to submicrometric domains.

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Review 6.  Single-Molecular Förster Resonance Energy Transfer Measurement on Structures and Interactions of Biomolecules.

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7.  A platform for combined DNA and protein microarrays based on total internal reflection fluorescence.

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Journal:  Sci Rep       Date:  2013       Impact factor: 4.379

9.  Crystallization around solid-like nanosized docks can explain the specificity, diversity, and stability of membrane microdomains.

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Review 10.  Membrane Rafts in T Cell Activation: A Spotlight on CD28 Costimulation.

Authors:  Sara Zumerle; Barbara Molon; Antonella Viola
Journal:  Front Immunol       Date:  2017-11-03       Impact factor: 7.561

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