Literature DB >> 2983767

Lipid-protein interactions in frog rod outer segment disc membranes. Characterization by spin labels.

R D Pates, A Watts, R Uhl, D Marsh.   

Abstract

Freely-diffusing phospholipid spin labels have been employed to study rhodopsin-lipid interactions in frog rod outer segment disc membranes. Examination of the ESR spectra leads us to the conclusion that there are two motionally distinguishable populations of lipid existing in frog rod outer segment membranes over a wide physiological temperature range. Each of the spin probes used shows a two-component electron spin resonance (ESR) spectrum, one component of which is motionally restricted on the ESR timescale, and represents between 33 and 40% of the total integrated spectral intensity. The second spectral component which accounts for the remainder of the spectral intensity possesses a lineshape characteristic of anisotropic motion in a lipid bilayer, very similar in shape to that observed from the same spin labels in dispersions of whole extracted frog rod outer segment lipid. The motionally restricted spectral component is attributed to those spin labels in contact with the surface of rhodospin, while the major component is believed to originate from spin labels in the fluid lipid bilayer region of the membranes. Calculations indicate that the motionally restricted lipid is sufficient to cover the protein surface. This population of lipids is shown here and elsewhere (Watts, A., Volotovski, I.D. and Marsh, D. (1979) Biochemistry 18, 5006-5013) to be by no means rigidly immobilized, having motion in the 20 ns time regime as opposed to motions in the one nanosecond time regime found in the fluid bilayer. Little selectivity for the motionally restricted population is observed between the different spin-labelled phospholipid classes nor with a spin-labelled fatty acid or sterol.

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Year:  1985        PMID: 2983767     DOI: 10.1016/0005-2736(85)90460-2

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  9 in total

Review 1.  Magnetic resonance of membranes.

Authors:  P F Knowles; D Marsh
Journal:  Biochem J       Date:  1991-03-15       Impact factor: 3.857

2.  Rhodopsin activation affects the environment of specific neighboring phospholipids: an FTIR spectroscopic study.

Authors:  J Isele; T P Sakmar; F Siebert
Journal:  Biophys J       Date:  2000-12       Impact factor: 4.033

3.  Stoichiometry of lipid interactions with transmembrane proteins--Deduced from the 3D structures.

Authors:  Tibor Páli; Denys Bashtovyy; Derek Marsh
Journal:  Protein Sci       Date:  2006-05       Impact factor: 6.725

4.  The role of charge in lipid selectivity for the nicotinic acetylcholine receptor.

Authors:  D E Raines; K W Miller
Journal:  Biophys J       Date:  1993-03       Impact factor: 4.033

Review 5.  Electron spin resonance in membrane research: protein-lipid interactions from challenging beginnings to state of the art.

Authors:  Derek Marsh
Journal:  Eur Biophys J       Date:  2009-08-11       Impact factor: 1.733

6.  A comparative spin-label study of isolated plasma membranes and plasma membranes of whole cells and protoplasts from cold-hardened and nonhardened winter rye.

Authors:  J J Windle
Journal:  Plant Physiol       Date:  1988-12       Impact factor: 8.340

7.  Selective detection of the rotational dynamics of the protein-associated lipid hydrocarbon chains in sarcoplasmic reticulum membranes.

Authors:  T C Squier; D D Thomas
Journal:  Biophys J       Date:  1989-10       Impact factor: 4.033

8.  Electron spin resonance studies of acyl chain motion in reconstituted nicotinic acetylcholine receptor membranes.

Authors:  D E Raines; G Wu; L A Dalton; K W Miller
Journal:  Biophys J       Date:  1995-08       Impact factor: 4.033

9.  Lateral pressure profile, spontaneous curvature frustration, and the incorporation and conformation of proteins in membranes.

Authors:  Derek Marsh
Journal:  Biophys J       Date:  2007-08-17       Impact factor: 4.033

  9 in total

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