Literature DB >> 2069956

Transbilayer distribution of bromine in fluid bilayers containing a specifically brominated analogue of dioleoylphosphatidylcholine.

M C Wiener1, S H White.   

Abstract

We describe in this paper the transbilayer distribution of the bromines of the specifically halogenated phospholipid 1-oleoyl-2-(9,10-dibromostearoyl)-sn-glycero-3- phosphocholine (OBPC). The distribution was determined by X-ray diffraction of oriented multilayers of mixtures of OBPC and 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) at 66% relative humidity by the general approach of Franks et al. (1978) [Nature 276, 530-532]. The bromine distribution of OBPC in the fluid L alpha phase is described accurately by a pair of Gaussian functions located 7.97 +/- 0.27 A from the center of the bilayer with l/e half-widths of 4.96 +/- 0.62 A. We find that OBPC bilayers are accurately described as DOPC bilayers with an additional bromine distribution centered at the position of the double bond of DOPC and conclude that OBPC is an excellent structural isomorph for DOPC under the conditions of these experiments. The distribution obtained is the complete and fully resolved transbilayer image of the halogen label because the broad distribution of the bromines is due entirely to thermal disorder and not to experimental limitations [Wiener, M. C., & White, S. H. (1991a) Biophys. J. 59, 162-173]. The observed width of the bromine distribution indicates that virtually all of the hydrocarbon interior is accessible to the bromines. The distance between the bromine/double-bond position and the headgroup phosphate position was determined from one-dimensional Patterson maps and found to be approximately 12 A. The application of accurately determined bromine distributions to the quantitative interpretation of fluorescence quenching experiments is discussed. A method for the self-consistent global analysis of diffraction data from mixtures that permits the use of data sets with different instrumental scale factors is developed in an Appendix.

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Year:  1991        PMID: 2069956     DOI: 10.1021/bi00242a027

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  25 in total

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2.  Experimental validation of molecular dynamics simulations of lipid bilayers: a new approach.

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4.  A membrane-translocating peptide penetrates into bilayers without significant bilayer perturbations.

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5.  Distribution analysis of membrane penetration of proteins by depth-dependent fluorescence quenching.

Authors:  A S Ladokhin; P W Holloway; E G Kostrzhevska
Journal:  J Fluoresc       Date:  1993-09       Impact factor: 2.217

6.  Cholesterol does not induce segregation of liquid-ordered domains in bilayers modeling the inner leaflet of the plasma membrane.

Authors:  T Y Wang; J R Silvius
Journal:  Biophys J       Date:  2001-11       Impact factor: 4.033

7.  Structure of a fluid dioleoylphosphatidylcholine bilayer determined by joint refinement of x-ray and neutron diffraction data. II. Distribution and packing of terminal methyl groups.

Authors:  M C Wiener; S H White
Journal:  Biophys J       Date:  1992-02       Impact factor: 4.033

8.  Structure of a fluid dioleoylphosphatidylcholine bilayer determined by joint refinement of x-ray and neutron diffraction data. III. Complete structure.

Authors:  M C Wiener; S H White
Journal:  Biophys J       Date:  1992-02       Impact factor: 4.033

9.  Bilayer interactions of pHLIP, a peptide that can deliver drugs and target tumors.

Authors:  Manuela Zoonens; Yana K Reshetnyak; Donald M Engelman
Journal:  Biophys J       Date:  2008-03-21       Impact factor: 4.033

10.  Structure and hydration of membranes embedded with voltage-sensing domains.

Authors:  Dmitriy Krepkiy; Mihaela Mihailescu; J Alfredo Freites; Eric V Schow; David L Worcester; Klaus Gawrisch; Douglas J Tobias; Stephen H White; Kenton J Swartz
Journal:  Nature       Date:  2009-11-26       Impact factor: 49.962

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