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Heterologously Expressed GLT-1 Associates in ~200-nm Protein-Lipid Islands

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Raunser,  Stefan
Department of Structural Biology, Max Planck Institute of Biophysics, Max Planck Society;

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Haase,  Winfried
Department of Structural Biology, Max Planck Institute of Biophysics, Max Planck Society;

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Kühlbrandt,  Werner       
Department of Structural Biology, Max Planck Institute of Biophysics, Max Planck Society;

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Citation

Raunser, S., Haase, W., Franke, C., Eckert, G., Müller, W. E., & Kühlbrandt, W. (2006). Heterologously Expressed GLT-1 Associates in ~200-nm Protein-Lipid Islands. Biophysical Journal (Annual Meeting Abstracts), 91, 3718-3726. doi:10.1529/biophysj.106.086900.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0024-D95C-9
Abstract
The glutamate transporter GLT-1 from Rattus norvegicus was expressed at high level in baby hamster kidney (BHK-21) cells by the Semliki Forest Virus expression system. We examined the expressed GLT-1 in the plasma membrane and found that the transporter accumulates in detergent-insoluble lipid-protein assemblies. Freeze-fracture, immunogold labeling, and electron microscopy revealed that GLT-1 forms approximately 200-nm protein-rich islands in the plasma membrane. Cholesterol depletion in living cells resulted in a dispersion of the GLT-1 islands, indicating that they are the result of lipid-protein rather than protein-protein interactions. Disruption of GLT-1 islands and dispersion of GLT-1 goes along with a reduction of the glutamate transport activity. Our direct visualization of lipid-protein islands in the plasma membrane of tissue culture cells suggests that the reported clustering of glutamate transporters and their cholesterol-dependent transport activity in cells is likewise connected to their association with cholesterol-rich microdomains in the plasma membrane.