Influence of length and conformation of saccharide head groups on the mechanics of glycolipid membranes: Unraveled by off-specular neutron scattering

被引:8
作者
Yamamoto, Akihisa [1 ,2 ]
Abuillan, Wasim [1 ]
Burk, Alexandra S. [1 ,3 ]
Koerner, Alexander [1 ]
Ries, Annika [4 ]
Werz, Daniel B. [5 ]
Deme, Bruno [6 ]
Tanaka, Motomu [1 ,2 ]
机构
[1] Heidelberg Univ, Inst Phys Chem, Phys Chem Biosyst, D-69120 Heidelberg, Germany
[2] Kyoto Univ, Inst Integrated Cell Mat Sci iCeMS, Kyoto 6068501, Japan
[3] Karlsruhe Inst Technol, Inst Toxicol & Genet, D-76021 Karlsruhe, Germany
[4] Univ Gottingen, Inst Organ & Biomol Chem, D-37077 Gottingen, Germany
[5] Tech Univ Carolo Wilhelmina Braunschweig, Inst Organ Chem, D-38106 Braunschweig, Germany
[6] Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
关键词
X-RAY-SCATTERING; ESCHERICHIA-COLI; GLOBO-H; MORPHOLOGY; BILAYERS; BINDING; MODEL;
D O I
10.1063/1.4918585
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The mechanical properties of multilayer stacks of Gb3 glycolipid that play key roles in metabolic disorders (Fabry disease) were determined quantitatively by using specular and off-specular neutron scattering. Because of the geometry of membrane stacks deposited on planar substrates, the scattered intensity profile was analyzed in a 2D reciprocal space map as a function of in-plane and out-of-plane scattering vector components. The two principal mechanical parameters of the membranes, namely, bending rigidity and compression modulus, can be quantified by full calculation of scattering functions with the aid of an effective cut-off radius that takes the finite sample size into consideration. The bulkier "bent" Gb3 trisaccharide group makes the membrane mechanics distinctly different from cylindrical disaccharide (lactose) head groups and shorter "bent" disaccharide (gentiobiose) head groups. The mechanical characterization of membranes enriched with complex glycolipids has high importance in understanding the mechanisms of diseases such as sphingolipidoses caused by the accumulation of non-degenerated glycosphingolipids in lysosomes or inhibition of protein synthesis triggered by the specific binding of Shiga toxin to Gb3. (C) 2015 Author(s).
引用
收藏
页数:8
相关论文
共 45 条
[1]  
[Anonymous], 1980, STAT PHYS 1
[2]   Cellular and tissue localization of globotriaosylceramide in Fabry disease [J].
Askari, Hasan ;
Kaneski, Christine R. ;
Semino-Mora, Cristina ;
Desai, Priya ;
Ang, Agnes ;
Kleiner, David E. ;
Perlee, Lorah T. ;
Quezado, Martha ;
Spollen, Linda E. ;
Wustman, Brandon A. ;
Schiffmann, Raphael .
VIRCHOWS ARCHIV, 2007, 451 (04) :823-834
[3]   Bilayer thickness and lipid interface area in unilamellar extruded 1,2-diacylphosphatidylcholine liposomes:: a small-angle neutron scattering study [J].
Balgavy, P ;
Dubnicková, M ;
Kucerka, N ;
Kiselev, MA ;
Yaradaikin, SP ;
Uhriková, D .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2001, 1512 (01) :40-52
[4]   Linear synthesis of the tumor-associated carbohydrate antigens globo-h, SSEA-3, and Gb3 [J].
Bosse, F ;
Marcaurelle, LA ;
Seeberger, PH .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (19) :6659-6670
[5]   FREQUENCY SPECTRUM OF FLICKER PHENOMENON IN ERYTHROCYTES [J].
BROCHARD, F ;
LENNON, JF .
JOURNAL DE PHYSIQUE, 1975, 36 (11) :1035-1047
[6]   Giant collective fluctuations of charged membranes at the lamellar-to-vesicle unbinding transition.: 1.: Characterization of a new lipid morphology by SANS, SAXS, and electron microscopy [J].
Demé, B ;
Dubois, M ;
Gulik-Krzywicki, T ;
Zemb, T .
LANGMUIR, 2002, 18 (04) :997-1004
[7]   Swelling of a lecithin lamellar phase induced by small carbohydrate solutes [J].
Demé, B ;
Dubois, M ;
Zemb, T .
BIOPHYSICAL JOURNAL, 2002, 82 (01) :215-225
[8]   Directed self-assembly of monodisperse phospholipid bilayer nanodiscs with controlled size [J].
Denisov, IG ;
Grinkova, YV ;
Lazarides, AA ;
Sligar, SG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (11) :3477-3487
[9]  
Derjaguin B.V., 1987, Surface Forces, DOI [10.1007/978-1-4757-6639-4, DOI 10.1007/978-1-4757-6639-4]
[10]  
Desnick R. J., 1995, METABOLIC MOL BASIS, VII, P2741