Data Entry: Please note that the research database will be replaced by UNIverse by the end of October 2023. Please enter your data into the system https://universe-intern.unibas.ch. Thanks

Login for users with Unibas email account...

Login for registered users without Unibas email account...

 
Thermodynamics of sodium dodecyl sulfate partitioning into lipid membranes
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 152976
Author(s) Tan, Anmin; Ziegler, André; Steinbauer, Bernhard; Seelig, Joachim
Author(s) at UniBasel Seelig, Joachim
Year 2002
Title Thermodynamics of sodium dodecyl sulfate partitioning into lipid membranes
Journal Biophysical journal
Volume 83
Number 3
Pages / Article-Number 1547-56
Keywords Anisotropy; Biophysics; Calorimetry; Cell Membrane/metabolism; Heat; Ions; Kinetics; Light; Lipid Bilayers/*chemistry; Lipids/chemistry; Magnetic Resonance Spectroscopy; Micelles; Models; Statistical; Scattering; Radiation; Sodium Dodecyl Sulfate/*chemistry; Temperature; Thermodynamics; Time Factors
Abstract The partition equilibria of sodium dodecyl sulfate (SDS) and lithium dodecyl sulfate between water and bilayer membranes were investigated with isothermal titration calorimetry and spectroscopic methods (light scattering, (31)P-nuclear magnetic resonance) in the temperature range of 28 degrees C to 56 degrees C. The partitioning of the dodecyl sulfate anion (DS(-)) into the bilayer membrane is energetically favored by an exothermic partition enthalpy of Delta H(O)(D) = -6.0 kcal/mol at 28 degrees C. This is in contrast to nonionic detergents where Delta H(O)(D) is usually positive. The partition enthalpy decreases linearly with increasing temperature and the molar heat capacity is Delta C(O)(P) = -50 +/- 3 cal mol(-1) K(-1). The partition isotherm is nonlinear if the bound detergent is plotted versus the free detergent concentration in bulk solution. This is caused by the electrostatic repulsion between the DS(-) ions inserted into the membrane and those free in solution near the membrane surface. The surface concentration of DS(-) immediately above the plane of binding was hence calculated with the Gouy-Chapman theory, and a strictly linear relationship was obtained between the surface concentration and the extent of DS(-) partitioning. The surface partition constant K describes the chemical equilibrium in the absence of electrostatic effects. For the SDS-membrane equilibrium K was found to be 1.2 x 10(4) M(-1) to 6 x 10(4) M(-1) for the various systems and conditions investigated, very similar to data available for nonionic detergents of the same chain length. The membrane-micelle phase diagram was also studied. Complete membrane solubilization requires a ratio of 2.2 mol SDS bound per mole of total lipid at 56 degrees C. The corresponding equilibrium concentration of SDS free in solution is C (sat)(D,F) approximately 1.7 mM and is slightly below the critical micelles concentration (CMC) = 2.1 mM (at 56 degrees C and 0.11 M buffer). Membrane saturation occurs at approximately 0.3 mol SDS per mol lipid and the equilibrium SDS concentration is C (sat)(D,F)approximately equal 2.2 mM +/- 0.6 mM. SDS translocation across the bilayer is slow at ambient temperature but increases at high temperatures.
Publisher Biophysical Society
ISSN/ISBN 0006-3495
edoc-URL http://edoc.unibas.ch/dok/A5257398
Full Text on edoc No
Digital Object Identifier DOI 10.1016/S0006-3495(02)73924-6
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/12202379
ISI-Number WOS:000177774500029
Document type (ISI) Journal Article
 
   

MCSS v5.8 PRO. 0.344 sec, queries - 0.000 sec ©Universität Basel  |  Impressum   |    
03/05/2024