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Light-induced reorganization of phospholipids in rod disc membranes
- Source :
- The Journal of biological chemistry. 276(4)
- Publication Year :
- 2000
-
Abstract
- The transbilayer redistribution of spin-labeled phospholipid analogues (SL-PL) with choline, serine, and ethanolamine head groups (PC, PS, and PE, respectively) was studied on intact disc vesicles of bovine rod outer segment membranes in the dark and after illumination. Redistribution was measured by the extraction of spin-labeled lipid analogues from the outer leaflet of membrane using the bovine serum albumin back-exchange assay. In the dark, PS was distributed asymmetrically, favoring the outer leaflet, whereas PC and PE showed small if any asymmetry. Green illumination for 1 min caused lipid head group-specific reorganization of SL-PL. Extraction of SL-PS by bovine serum albumin showed a fast transient (10 min) enhancement, which was further augmented by a peptide stabilizing the active metarhodopsin II conformation. The data suggest a direct release of 1 molecule of bound PS per rhodopsin into the outer leaflet and subsequent redistribution between the two leaflets. SL-PE and SL-PC showed more complex kinetics, in both cases consistent with a prolonged period of reduced extraction (2 phospholipids per rhodopsin in each case). The different phases of SL-PL reorganization after illumination may be related to the formation and decay of the active rhodopsin species and to their subsequent regeneration process.
- Subjects :
- Rhodopsin
Light
Phospholipid
Phosphatidylserines
Biochemistry
Serine
chemistry.chemical_compound
Ethanolamine
Choline
Animals
Transducin
Bovine serum albumin
Molecular Biology
Phospholipids
Chromatography
biology
Vesicle
Phosphatidylethanolamines
Biological Transport
Cell Biology
Rod Cell Outer Segment
Peptide Fragments
Membrane
chemistry
Light induced
biology.protein
Phosphatidylcholines
Cattle
Spin Labels
Subjects
Details
- ISSN :
- 00219258
- Volume :
- 276
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- The Journal of biological chemistry
- Accession number :
- edsair.doi.dedup.....b60c5625bb183aaac3296aa32a853ee9