Literature DB >> 9394007

Sphingolipid organization in biomembranes: what physical studies of model membranes reveal.

R E Brown1.   

Abstract

Recent cell biological studies suggest that sphingolipids and cholesterol may cluster in biomembranes to form raft-like microdomains. Such lipid domains are postulated to function as platforms involved in the lateral sorting of certain proteins during their trafficking within cells as well as during signal transduction events. Here, the physical interactions that occur between cholesterol and sphingolipids in model membrane systems are discussed within the context of microdomain formation. A model is presented in which the role of cholesterol is refined compared to earlier models.

Entities:  

Mesh：

Substances：

Year:  1998        PMID： 9394007      PMCID： PMC4043137          DOI： 10.1242/jcs.111.1.1

Source DB:  PubMed          Journal:  J Cell Sci        ISSN： 0021-9533            Impact factor:   5.285


  108 in total

1.  Guilty by insolubility--does a protein's detergent insolubility reflect a caveolar location?

Authors:  T V Kurzchalia; E Hartmann; P Dupree
Journal:  Trends Cell Biol       Date:  1995-05       Impact factor: 20.808

Review 2.  Caveolae and caveolins.

Authors:  R G Parton
Journal:  Curr Opin Cell Biol       Date:  1996-08       Impact factor: 8.382

3.  Globoside as a membrane receptor: a consideration of oligosaccharide communication with the hydrophobic domain.

Authors:  D H Jones; C A Lingwood; K R Barber; C W Grant
Journal:  Biochemistry       Date:  1997-07-15       Impact factor: 3.162

4.  Organization of the glycosphingolipid asialo-GM1 in phosphatidylcholine bilayers.

Authors:  T W Tillack; M Wong; M Allietta; T E Thompson
Journal:  Biochim Biophys Acta       Date:  1982-10-07

5.  Orientation of the saccharide chains of glycolipids at the membrane surface: conformational analysis of the glucose-ceramide and the glucose-glyceride linkages using molecular mechanics (MM3).

Authors:  P G Nyholm; I Pascher
Journal:  Biochemistry       Date:  1993-02-09       Impact factor: 3.162

6.  Glycosphingolipid fatty acid arrangement in phospholipid bilayers: cholesterol effects.

Authors:  M R Morrow; D Singh; D Lu; C W Grant
Journal:  Biophys J       Date:  1995-01       Impact factor: 4.033

7.  Thermotropic behavior of binary mixtures of dipalmitoylphosphatidylcholine and glycosphingolipids in aqueous dispersions.

Authors:  B Maggio; T Ariga; J M Sturtevant; R K Yu
Journal:  Biochim Biophys Acta       Date:  1985-08-08

8.  Simplified derivatization for determining sphingolipid fatty acyl composition by gas chromatography-mass spectrometry.

Authors:  S B Johnson; R E Brown
Journal:  J Chromatogr       Date:  1992-07-17

Review 9.  Intrinsic molecules in lipid membranes change the lipid-domain interfacial area: cholesterol at domain interfaces.

Authors:  L Cruzeiro-Hansson; J H Ipsen; O G Mouritsen
Journal:  Biochim Biophys Acta       Date:  1989-02-27

10.  Fluorescence evidence for cholesterol regular distribution in phosphatidylcholine and in sphingomyelin lipid bilayers.

Authors:  P L Chong; F Liu; M M Wang; K Truong; I P Sugar; R E Brown
Journal:  J Fluoresc       Date:  1996-12       Impact factor: 2.217
View more
  126 in total

Review 1.  Signaling through sphingolipid microdomains of the plasma membrane: the concept of signaling platform.

Authors:  D C Hoessli; S Ilangumaran; A Soltermann; P J Robinson; B Borisch
Journal:  Glycoconj J       Date:  2000 Mar-Apr       Impact factor: 2.916

2.  Cytoskeleton-dependent membrane domain segregation during neutrophil polarization.

Authors:  S Seveau; R J Eddy; F R Maxfield; L M Pierini
Journal:  Mol Biol Cell       Date:  2001-11       Impact factor: 4.138

3.  Cholesterol decreases the interfacial elasticity and detergent solubility of sphingomyelins.

Authors:  X M Li; M M Momsen; J M Smaby; H L Brockman; R E Brown
Journal:  Biochemistry       Date:  2001-05-22       Impact factor: 3.162

4.  Charged membrane surfaces impede the protein-mediated transfer of glycosphingolipids between phospholipid bilayers.

Authors:  P Mattjus; H M Pike; J G Molotkovsky; R E Brown
Journal:  Biochemistry       Date:  2000-02-08       Impact factor: 3.162

5.  Borrelia burgdorferi HtrA: evidence for twofold proteolysis of outer membrane protein p66.

Authors:  James L Coleman; Alvaro Toledo; Jorge L Benach
Journal:  Mol Microbiol       Date:  2015-10-20       Impact factor: 3.501

6.  Insights into the role of specific lipids in the formation and delivery of lipid microdomains to the plasma membrane of plant cells.

Authors:  Maryse Laloi; Anne-Marie Perret; Laurent Chatre; Su Melser; Catherine Cantrel; Marie-Noëlle Vaultier; Alain Zachowski; Katell Bathany; Jean-Marie Schmitter; Myriam Vallet; René Lessire; Marie-Andrée Hartmann; Patrick Moreau
Journal:  Plant Physiol       Date:  2006-11-17       Impact factor: 8.340

7.  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

Review 8.  Phase diagrams of lipid mixtures relevant to the study of membrane rafts.

Authors:  Félix M Goñi; Alicia Alonso; Luis A Bagatolli; Rhoderick E Brown; Derek Marsh; Manuel Prieto; Jenifer L Thewalt
Journal:  Biochim Biophys Acta       Date:  2008-10-07

9.  High-resolution proton NMR measures mobile lipids associated with Triton-resistant membrane domains in haematopoietic K562 cells lacking or expressing caveolin-1.

Authors:  A Ferretti; A Knijn; C Raggi; M Sargiacomo
Journal:  Eur Biophys J       Date:  2003-01-28       Impact factor: 1.733

10.  L718P mutation in the membrane-proximal cytoplasmic tail of beta 3 promotes abnormal alpha IIb beta 3 clustering and lipid microdomain coalescence, and associates with a thrombasthenia-like phenotype.

Authors:  Asier Jayo; Isabel Conde; Pedro Lastres; Constantino Martínez; José Rivera; Vicente Vicente; Consuelo González-Manchón
Journal:  Haematologica       Date:  2010-01-15       Impact factor: 9.941
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.