Temperature and ionic strength dependent light scattering of DMPG dispersions

被引:55
作者
Riske, KA
Politi, MJ
Reed, WF
LamyFreund, MT
机构
[1] UNIV SAO PAULO,INST PHYS,BR-05315970 SAO PAULO,BRAZIL
[2] UNIV SAO PAULO,INST CHEM,SAO PAULO,BRAZIL
[3] TULANE UNIV,DEPT PHYS,NEW ORLEANS,LA 70118
基金
巴西圣保罗研究基金会;
关键词
DMPG; light scattering; ionic strength; phase transition; surface ionization;
D O I
10.1016/S0009-3084(97)00058-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The temperature dependence of the intensity of light scattered by aqueous dispersions of the anionic lipid DMPG (dimyristoyl phosphatidylglycerol) was studied at different ionic strengths. The lipid main transition, gel-liquid crystal, is clearly detected by a sharp decrease in light scattering. As expected, the temperature of the main transition (T-m) was found to increase with the increase of the ionic strength. For low ionic strength, a DMPG second temperature transition, termed the 'post-transition', can be monitored by both an increase in light scattering and a decrease in conductivity. Zimm plot analysis indicates that below T-m the liposomes tend to aggregate, and show a negative second virial coefficient A(2), and particles of large molecular weight. At the main phase transition, parallel to the decrease in light scattering, there is an increase in the sample conductivity, A(2) becomes positive and the particle molecular weight decreases, indicating that the vesicles become disaggregated. Moreover, at the post-transition (T-post) A(2) becomes very small, perhaps slightly negative, and the molecular weight increases again. Both the main and the post transitions were found to be reversible. In contrast to the main transition, the post-transition could not be detected by spin labels placed either at the membrane surface, or in the-bilayer core. While the mechanism of increased ionization at T-m could be related to the melting of the hydrocarbon chains, the mechanism for the possible counterions recondensation at T-post is far less clear. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:31 / 44
页数:14
相关论文
共 45 条
[1]  
Biaggi MH, 1996, EUR BIOPHYS J BIOPHY, V24, P251
[2]   TITRATION OF THE PHASE-TRANSITION OF PHOSPHATIDYLSERINE BILAYER-MEMBRANES - EFFECTS OF PH, SURFACE ELECTROSTATICS, ION BINDING, AND HEADGROUP HYDRATION [J].
CEVC, G ;
WATTS, A ;
MARSH, D .
BIOCHEMISTRY, 1981, 20 (17) :4955-4965
[3]   NON-ELECTROSTATIC CONTRIBUTION TO THE TITRATION OF THE ORDERED-FLUID PHASE-TRANSITION OF PHOSPHATIDYLGLYCEROL BILAYERS [J].
CEVC, G ;
WATTS, A ;
MARSH, D .
FEBS LETTERS, 1980, 120 (02) :267-270
[4]  
Conway B.E., 1981, Ionic Hydration in Chemistry and Biophysics
[5]   A THEORY OF EFFECTS OF PROTONS AND DIVALENT-CATIONS ON PHASE-EQUILIBRIA IN CHARGED BILAYER-MEMBRANES - COMPARISON WITH EXPERIMENT [J].
COPELAND, BR ;
ANDERSEN, HC .
BIOCHEMISTRY, 1982, 21 (12) :2811-2820
[6]   OPTICAL-PROPERTIES OF LIPID DISPERSIONS INDUCED BY PERMEANT MOLECULES [J].
DISALVO, EA .
CHEMISTRY AND PHYSICS OF LIPIDS, 1991, 59 (03) :199-206
[7]   ADSORPTION OF MONO-VALENT CATIONS TO BILAYER MEMBRANES CONTAINING NEGATIVE PHOSPHOLIPIDS [J].
EISENBERG, M ;
GRESALFI, T ;
RICCIO, T ;
MCLAUGHLIN, S .
BIOCHEMISTRY, 1979, 18 (23) :5213-5223
[8]   EFFECT OF ELECTROSTATIC REPULSION ON THE MORPHOLOGY AND THERMOTROPIC TRANSITIONS OF ANIONIC PHOSPHOLIPIDS [J].
EPAND, RM ;
HUI, SW .
FEBS LETTERS, 1986, 209 (02) :257-260
[9]   FORMATION OF A NEW STABLE PHASE OF PHOSPHATIDYLGLYCEROLS [J].
EPAND, RM ;
GABEL, B ;
EPAND, RF ;
SEN, A ;
HUI, SW ;
MUGA, A ;
SUREWICZ, WK .
BIOPHYSICAL JOURNAL, 1992, 63 (02) :327-332
[10]   EQUILIBRIUM STUDIES OF PHOSPHOLIPID-BILAYER ASSEMBLY - COEXISTENCE OF SURFACE BILAYERS AND UNILAMELLAR VESICLES [J].
GERSHFELD, NL ;
STEVENS, WF ;
NOSSAL, RJ .
FARADAY DISCUSSIONS, 1986, 81 :19-28