Membrane protein sequestering by ionic protein–lipid interactions

被引:0
|
作者
Geert van den Bogaart
Karsten Meyenberg
H. Jelger Risselada
Hayder Amin
Katrin I. Willig
Barbara E. Hubrich
Markus Dier
Stefan W. Hell
Helmut Grubmüller
Ulf Diederichsen
Reinhard Jahn
机构
[1] Max Planck Institute for Biophysical Chemistry,Department of Neurobiology
[2] Am Faßberg 11,Department of Theoretical and Computational Biophysics
[3] Institute for Organic and Biomolecular Chemistry,Department of Nanobiophotonics
[4] Georg-August-University Göttingen,undefined
[5] Tammannstraße 2,undefined
[6] Max Planck Institute for Biophysical Chemistry,undefined
[7] Am Faßberg 11,undefined
[8] Max Planck Institute for Biophysical Chemistry,undefined
[9] Am Faßberg 11,undefined
来源
Nature | 2011年 / 479卷
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摘要
Exocytosis in neuronal cells requires the SNARE protein syntaxin-1A, which is clustered at sites where synaptic vesicles are poised to undergo exocytosis. Reinhard Jahn and colleagues use super-resolution stimulated-emission depletion (STED) microscopy to show that syntaxin clusters in the membrane through electrostatic interactions with the strongly anionic lipid phosphatidylinositol-4,5-bisphosphate (PIP2) into 70-nanometre microdomains. The results demonstrate that electrostatic protein–lipid interactions can result in the formation of microdomains independent of cholesterol or lipid phases and have important implications for the organization of the plasma membrane.
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页码:552 / 555
页数:3
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