A diglucosylated fluorinated surfactant to handle integral membrane proteins in aqueous solution

被引:15
作者
Abla, Maher [1 ]
Durand, Gregory [1 ,2 ]
Breyton, Cecile [3 ,4 ,5 ]
Raynal, Simon [1 ,2 ]
Ebel, Christine [3 ,4 ,5 ]
Pucci, Bernard [1 ,2 ]
机构
[1] Univ Avignon & Pays de Vaucluse, Equipe Chim Bioorgan & Syst Amphiphiles, F-84000 Avignon, France
[2] Inst Biomol Max Mousseron, UMR 5247, F-34093 Montpellier 05, France
[3] CEA, IBS, F-38027 Grenoble, France
[4] CNRS, UMR 5075, IBS, Grenoble, France
[5] Univ Grenoble 1, IBS, Grenoble, France
关键词
Fluorinated surfactants; Micelles; Membrane proteins; HEMIFLUORINATED SURFACTANTS; NONIONIC SURFACTANTS; ANALYTICAL ULTRACENTRIFUGATION; AMPHIPOLS; FLUOROCARBON; DETERGENTS; PEPTIDE; TAILS; SIZE;
D O I
10.1016/j.jfluchem.2011.05.015
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The use of fluorinated surfactants as efficient tools for handling membrane proteins in aqueous media was demonstrated many years ago. The work reported herein deals with the synthesis of a new sugar-based surfactant bearing two glucose moieties and labelled F-6-DigluM. The synthesis of F-6-DigluM is based on a one-pot reduction/alkylation of a fluorinated thioacetate onto an acrylamido-type polar head precursor, using NaBH4 in refluxing methanol. Its physical-chemical properties in aqueous solution were studied by surface tension measurement, dynamic light scattering and analytical ultracentrifugation. F-6-DigluM exhibits a critical micellar concentration of similar to 0.4 mM and self-assembles into small and well-defined aggregates, very likely to globular micelles. Finally, the homogeneity and the stability of complexes of bacteriorhodopsin and F-6-DigluM over time were observed, demonstrating that F-6-DigluM is a suitable tool for biochemical applications. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:63 / 71
页数:9
相关论文
共 47 条
[1]   Glucose-Based Surfactants with Hydrogenated, Fluorinated, or Hemifluorinated Tails: Synthesis and Comparative Physical-Chemical Characterization [J].
Abla, Maher ;
Durand, Grgory ;
Pucci, Bernard .
JOURNAL OF ORGANIC CHEMISTRY, 2008, 73 (21) :8142-8153
[2]   Fluorocarbon -: Hydrocarbon nonionic surfactants mixtures:: A study of their miscibility [J].
Barthélèmy, P ;
Tomao, V ;
Selb, J ;
Chaudier, Y ;
Pucci, B .
LANGMUIR, 2002, 18 (07) :2557-2563
[3]   Synthesis and preliminary assessments of ethyl-terminated perfluoroalkyl nonionic surfactants derived from tris(hydroxymethyl)acrylamidomethane [J].
Barthélémy, P ;
Ameduri, B ;
Chabaud, E ;
Popot, JL ;
Pucci, B .
ORGANIC LETTERS, 1999, 1 (11) :1689-1692
[4]  
Baumann T., 1986, J CHROMATOGR, V373, P191
[5]   Trapping and Stabilization of Integral Membrane Proteins by Hydrophobically Grafted Glucose-Based Telomers [J].
Bazzacco, Paola ;
Sharma, K. Shivaji ;
Durand, Gregory ;
Giusti, Fabrice ;
Ebel, Christine ;
Popot, Jean-Luc ;
Pucci, Bernard .
BIOMACROMOLECULES, 2009, 10 (12) :3317-3326
[6]   A NEW CONVENIENT REAGENT FOR PEPTIDE SYNTHESES [J].
BELLEAU, B ;
MALEK, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (06) :1651-&
[7]   Hemifluorinated surfactants: a non-dissociating environment for handling membrane proteins in aqueous solutions? [J].
Breyton, C ;
Chabaud, E ;
Chaudier, Y ;
Pucci, B ;
Popot, JL .
FEBS LETTERS, 2004, 564 (03) :312-318
[8]  
Breyton C, 2010, METHODS MOL BIOL, V601, P219, DOI 10.1007/978-1-60761-344-2_14
[9]   Micellar and Biochemical Properties of (Hemi)Fluorinated Surfactants Are Controlled by the Size of the Polar Head [J].
Breyton, Cecile ;
Gabel, Frank ;
Abla, Maher ;
Pierre, Yves ;
Lebaupain, Florence ;
Durand, Gregory ;
Popot, Jean-Luc ;
Ebel, Christine ;
Pucci, Bernard .
BIOPHYSICAL JOURNAL, 2009, 97 (04) :1077-1086
[10]   Stabilization of integral membrane proteins in aqueous solution using fluorinated surfactants [J].
Chabaud, E ;
Barthélémy, P ;
Mora, N ;
Popot, JL ;
Pucci, B .
BIOCHIMIE, 1998, 80 (5-6) :515-530