Abstract
A new technique for the measurement of membrane surface potential is proposed and demonstrated. The method is based on the fact that a positively charged styryl dye molecule aggregates when present at high concentration in the Debye layer near a membrane bearing a negative surface potential. The dye in its aggregated form exhibits marked differences in its resonance Raman spectrum relative to the free dye molecules. This method was used to study the potential on the surfaces of the purple membrane that contains the pigment bacteriorhodopsin. A value of -29.5 mV was found for membranes with bacteriorhodopsin in its relaxed, light-adapted state, and the potential decreased to -34.5 mV when most of the bacteriorhodopsin was converted to the M412 intermediate. Because the dye probe does not diffuse through the lipid bilayer, it can be used to probe the potential on the external or internal surface of a vesicle. Thus, we found that the potential on the purple membrane was asymmetric and was localized mainly on the surface that faces the cytoplasm in the cell.
Original language | English |
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Pages (from-to) | 663-670 |
Number of pages | 8 |
Journal | Biophysical Journal |
Volume | 45 |
Issue number | 4 |
DOIs | |
State | Published - Apr 1984 |
Bibliographical note
Funding Information:This research was supported by a grant from the U.S.-Israel Binational Science Foundation, Jerusalem, Israel.
Funding
This research was supported by a grant from the U.S.-Israel Binational Science Foundation, Jerusalem, Israel.
Funders | Funder number |
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U.S.-Israel Binational Science Foundation |