Literature DB >> 16852481

Water concentration profiles in membranes measured by ESEEM of spin-labeled lipids.

Denis A Erilov1, Rosa Bartucci, Rita Guzzi, Alexander A Shubin, Alexander G Maryasov, Derek Marsh, Sergei A Dzuba, Luigi Sportelli.   

Abstract

Electron spin-echo envelope modulation (ESEEM) spectroscopy of phospholipids spin-labeled systematically down the sn-2 chain was used to detect the penetration of water (D2O) into bilayer membranes of dipalmitoyl phosphatidylcholine with and without 50 mol % cholesterol. Three-pulse stimulated echoes allow the resolution of two superimposed 2H-ESEEM spectral components of different widths, for spin labels located in the upper part of the lipid chains. Quantum chemical calculations (DFT) and ESEEM simulations assign the broad spectral component to one or two D2O molecules that are directly hydrogen bonded to the N-O group of the spin label. Classical ESEEM simulations establish that the narrow spectral component arises from nonbonded water (D2O) molecules that are free in the hydrocarbon chain region of the bilayer membrane. The amplitudes of the broad 2H-ESEEM spectral component correlate directly with those of the narrow component for spin labels at different positions down the lipid chain, reflecting the local H-bonding equilibria. The D2O-ESEEM amplitudes decrease with position down the chain toward the bilayer center, displaying a sigmoidal dependence on position that is characteristic of transmembrane polarity profiles established by other less direct spin-labeling methods. The midpoint of the sigmoidal profile is shifted toward the membrane center for membranes without cholesterol, relative to those with cholesterol, and the D2O-ESEEM amplitude in the outer regions of the chain is greater in the presence of cholesterol than in its absence. For both membrane types, the D2O amplitude is almost vanishingly small at the bilayer center. The water-penetration profiles reverse correlate with the lipid-chain packing density, as reflected by 1H-ESEEM intensities from protons of the membrane matrix. An analysis of the H-bonding equilibria provides essential information on the binding of water molecules to H-bond acceptors within the hydrophobic interior of membranes. For membranes containing cholesterol, approximately 40% of the nitroxides in the region adjacent to the lipid headgroups are H bonded to water, of which ca. 15% are doubly H bonded. Corresponding H-bonded populations in membranes without cholesterol are ca. 20%, of which ca. 6% are doubly bonded.

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Year:  2005        PMID: 16852481     DOI: 10.1021/jp050886z

Source DB:  PubMed          Journal:  J Phys Chem B        ISSN: 1520-5207            Impact factor:   2.991


  31 in total

1.  Location and aggregation of the spin-labeled peptide trichogin GA IV in a phospholipid membrane as revealed by pulsed EPR.

Authors:  E S Salnikov; D A Erilov; A D Milov; Yu D Tsvetkov; C Peggion; F Formaggio; C Toniolo; J Raap; S A Dzuba
Journal:  Biophys J       Date:  2006-06-02       Impact factor: 4.033

2.  Utilizing ESEEM spectroscopy to locate the position of specific regions of membrane-active peptides within model membranes.

Authors:  Raanan Carmieli; Niv Papo; Herbert Zimmermann; Alexey Potapov; Yechiel Shai; Daniella Goldfarb
Journal:  Biophys J       Date:  2005-10-28       Impact factor: 4.033

3.  Positioning of proteins in membranes: a computational approach.

Authors:  Andrei L Lomize; Irina D Pogozheva; Mikhail A Lomize; Henry I Mosberg
Journal:  Protein Sci       Date:  2006-06       Impact factor: 6.725

4.  Geometry of hydrogen bonds formed by lipid bilayer nitroxide probes: a high-frequency pulsed ENDOR/EPR study.

Authors:  Tatyana I Smirnova; Alex I Smirnov; Serguei V Paschenko; Oleg G Poluektov
Journal:  J Am Chem Soc       Date:  2007-03-07       Impact factor: 15.419

5.  Structure of self-aggregated alamethicin in ePC membranes detected by pulsed electron-electron double resonance and electron spin echo envelope modulation spectroscopies.

Authors:  Alexander D Milov; Rimma I Samoilova; Yuri D Tsvetkov; Marta De Zotti; Fernando Formaggio; Claudio Toniolo; Jan-Willem Handgraaf; Jan Raap
Journal:  Biophys J       Date:  2009-04-22       Impact factor: 4.033

6.  Reaction fields in the environment of fluorescent probes: polarity profiles in membranes.

Authors:  Derek Marsh
Journal:  Biophys J       Date:  2009-04-08       Impact factor: 4.033

7.  Structural adaptations of proteins to different biological membranes.

Authors:  Irina D Pogozheva; Stephanie Tristram-Nagle; Henry I Mosberg; Andrei L Lomize
Journal:  Biochim Biophys Acta       Date:  2013-06-27

8.  Spin-Label EPR for Determining Polarity and Proticity in Biomolecular Assemblies: Transmembrane Profiles.

Authors:  Derek Marsh
Journal:  Appl Magn Reson       Date:  2009-11-17       Impact factor: 0.831

9.  Pulsed EPR determination of water accessibility to spin-labeled amino acid residues in LHCIIb.

Authors:  A Volkov; C Dockter; T Bund; H Paulsen; G Jeschke
Journal:  Biophys J       Date:  2009-02       Impact factor: 4.033

10.  Intramembrane water associated with TOAC spin-labeled alamethicin: electron spin-echo envelope modulation by D2O.

Authors:  R Bartucci; R Guzzi; L Sportelli; D Marsh
Journal:  Biophys J       Date:  2009-02       Impact factor: 4.033

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