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PubMed · 15295640

Laser-assisted fluorescence microscopy for measuring cell membrane dynamics.

Herbert Schneckenburger·Michael Wagner·Martina Kretzschmar·Wolfgang S L Strauss·Reinhard Sailer
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Abstract

Membranes of living cells are characterized by laser-assisted fluorescence microscopy, in particular a combination of microspectrofluorometry, total internal reflection fluorescence microscopy (TIRFM), fluorescence lifetime imaging (FLIM) and Forster resonance energy transfer (FRET) spectroscopy. The generalized polarization (GP, characterizing a spectral shift which depends on the phase of membrane lipids) as well as the effective fluorescence lifetime (tau(eff)) of the membrane marker laurdan were revealed to be appropriate parameters for membrane stiffness and fluidity. GP decreased with temperature, but increased during cell growth and was always higher for the plasma membrane than for intracellular membranes. Microdomains of different fluorescence lifetimes tau(eff) were observed at temperatures above 30 degree C and disappeared during cell aging. Non-radiative energy transfer was used to detect laurdan selectively in close proximity to a molecular acceptor (DiI) and may present a possibility for measuring membrane dynamics in specific microenvironments.

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AnimalsCHO CellsCell DivisionCell MembraneCricetinaeHalf-LifeLasersMembrane FluidityMembrane MicrodomainsMicroscopy, FluorescenceSpectrometry, FluorescenceTemperatureJournal ArticleResearch Support, Non-U.S. Gov't

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Herbert Schneckenburger, Michael Wagner, Martina Kretzschmar, Wolfgang S L Strauss, Reinhard Sailer. 2004-05-28. Laser-assisted fluorescence microscopy for measuring cell membrane dynamics.. https://doi.org/10.1039/b317047k

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