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Lateral Mobility of Membrane-Binding Proteins in Living Cells Measured by Total Internal Reflection Fluorescence Correlation Spectroscopy

Yu Ohsugi ^*, Kenta Saito , Mamoru Tamura ^* and Masataka Kinjo ^*

Laboratory of ^* Supramolecular Biophysics and Nanosystems Physiology, Research Institute for Electronic Science, Hokkaido University, Sapporo, Japan

Correspondence: Address reprint requests to Masataka Kinjo, Tel.: 81-11-706-2890; E-mail: kinjo{at}imd.es.hokudai.ac.jp.

Total internal reflection fluorescence correlation spectroscopy (TIR-FCS) allows us to measure diffusion constants and the number of fluorescent molecules in a small area of an evanescent field generated on the objective of a microscope. The application of TIR-FCS makes possible the characterization of reversible association and dissociation rates between fluorescent ligands and their receptors in supported phospholipid bilayers. Here, for the first time, we extend TIR-FCS to a cellular application for measuring the lateral diffusion of a membrane-binding fluorescent protein, farnesylated EGFP, on the plasma membranes of cultured HeLa and COS7 cells. We detected two kinds of diffusional motion—fast three-dimensional diffusion (D₁) and much slower two-dimensional diffusion (D₂), simultaneously. Conventional FCS and single-molecule tracking confirmed that D₁ was free diffusion of farnesylated EGFP close to the plasma membrane in cytosol and D₂ was lateral diffusion in the plasma membrane. These results suggest that TIR-FCS is a powerful technique to monitor movement of membrane-localized molecules and membrane dynamics in living cells.

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