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Effects on capacitance by overexpression of membrane proteins
Authors:Zimmermann D  Zhou A  Kiesel M  Feldbauer K  Terpitz U  Haase W  Schneider-Hohendorf T  Bamberg E  Sukhorukov V L
Affiliation:a Department of Biophysical Chemistry, Max-Planck-Institute of Biophysics, Max-von-Laue-Strasse 3, 60438 Frankfurt am Main, Germany
b Department of Biophysical Chemistry, Chemistry and Pharmacy, Johann-Wolfgang-Goethe University, Max-von-Laue-Strasse 4, 60438 Frankfurt am Main, Germany
c Department of Cell Physiology, Max-Planck-Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany
d Department of Biotechnology, University of Würzburg, Am Hubland, 97074 Würzburg, Germany
e Department of Structural Biology, Max-Planck-Institute of Biophysics, Max-von-Laue-Strasse 3, 60438 Frankfurt am Main, Germany
Abstract:Functional Channelrhodopsin-2 (ChR2) overexpression of about 104 channels/μm2 in the plasma membrane of HEK293 cells was studied by patch-clamp and freeze-fracture electron microscopy. Simultaneous electrorotation measurements revealed that ChR2 expression was accompanied by a marked increase of the area-specific membrane capacitance (Cm). The Cm increase apparently resulted partly from an enlargement of the size and/or number of microvilli. This is suggested by a relatively large Cm of 1.15 ± 0.08 μF/cm2 in ChR2-expressing cells measured under isotonic conditions. This value was much higher than that of the control HEK293 cells (0.79 ± 0.02 μF/cm2). However, even after complete loss of microvilli under strong hypoosmolar conditions (100 mOsm), the ChR2-expressing cells still exhibited a significantly larger Cm (0.85 ± 0.07 μF/cm2) as compared to non-expressing control cells (0.70 ± 0.03 μF/cm2). Therefore, a second mechanism of capacitance increase may involve changes in the membrane permittivity and/or thickness due to the embedded ChR2 proteins.
Keywords:Patch-clamp   Electrorotation   Freeze-fracture electron microscopy   HEK293   Overexpression   Membrane capacitance   Channelrhodopsin-2
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