Complexation between DNA and surfactants and lipids: phase behavior and molecular organization

被引:33
作者
Bilalov, Azat [1 ]
Olsson, Ulf [1 ]
Lindman, Bjoern [1 ,2 ]
机构
[1] Lund Univ, SE-22100 Lund, Sweden
[2] Univ Coimbra, Dept Chem, P-3004535 Coimbra, Portugal
基金
瑞典研究理事会;
关键词
BETA-CYCLODEXTRIN; IONIC SURFACTANTS; WATER; MICELLES; POLYELECTROLYTES; DYNAMICS; DRUGS;
D O I
10.1039/c2sm26553b
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 interaction between DNA and various cationic species, e. g. cationic surfactant (CS), has a broad biological and biotechnological significance. In the cell nucleus as well as in transfection formulations, other species, mainly zwitterionic lipids, are also present but their exact role needs elucidation. A closer investigation of the stability of structures formed as well as the molecular arrangements is hampered by the complexity of the systems with respect to the number of components. A powerful way for reducing the number of components is to base studies on the stoichiometric (1 : 1) compound CSDNA, where the simple (sodium) counterions have been ion-exchanged by a cationic amphiphile ion. CSDNA is typically insoluble in water but is able to form liquid crystalline phases in aqueous mixtures with many additives capable of associating with the amphiphilic counterions (alcohols, non-ionic surfactants, lipids, cyclodextrins, etc.). Mixtures of CSDNA with a number of components have been investigated in detail with respect to phase behavior. The phase diagrams demonstrate a rich liquid crystallinity. The organization of DNA and the surfactant-lipid self-assemblies is controlled by different factors for different cases, mainly (i) the lipophilic characteristics of the components, (ii) the [CSDNA]/[amphiphile] ratio and (iii) DNA packing constraints, due to the large persistence length. A summary of phase diagrams is presented together with structural investigations based mainly on small-angle X-ray scattering. The role of DNA rigidity is illustrated in a comparison with analogous systems based on flexible polyanions.
引用
收藏
页码:11022 / 11033
页数:12
相关论文
共 66 条
[11]   Electrostatics of DNA cationic lipid complexes: isoelectric instability [J].
Bruinsma, R .
EUROPEAN PHYSICAL JOURNAL B, 1998, 4 (01) :75-88
[12]   The interactions between nonionic surfactants and cyclodextrins studied by fluorescence measurements [J].
Buschmann, HJ ;
Cleve, E ;
Schollmeyer, E .
JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY, 1999, 33 (02) :233-241
[13]   Aqueous phase behavior of polyelectrolytes with amphiphilic counterions modulated by cyclodextrin: the role of polyion flexibility [J].
Carlstedt, Jonas ;
Bilalov, Azat ;
Olsson, Ulf .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2012, 14 (27) :9574-9577
[14]   Cyclodextrin-Surfactant Coassembly Depends on the Cyclodextrin Ability To Crystallize [J].
Carlstedt, Jonas ;
Bilalov, Azat ;
Krivtsova, Elena ;
Olsson, Ulf ;
Lindman, Bjorn .
LANGMUIR, 2012, 28 (05) :2387-2394
[15]  
Chrzanowska A, 2005, ACTA PHYS POL B, V36, P3163
[16]   Velocity correlations of two-dimensional hard needles from molecular dynamics [J].
Chrzanowska, A ;
Ehrentraut, H .
PHYSICAL REVIEW E, 2002, 66 (01) :1-012201
[17]   The stability of cyclodextrin complexes in solution [J].
Connors, KA .
CHEMICAL REVIEWS, 1997, 97 (05) :1325-1357
[18]   DNA that is dispersed in the liquid crystalline phases of phospholipids is actively transcribed [J].
Corsi, Josephine ;
Dymond, Marcus K. ;
Ces, Oscar ;
Muck, Joscha ;
Zink, Daniele ;
Attard, George S. .
CHEMICAL COMMUNICATIONS, 2008, (20) :2307-2309
[19]   Osmotically Induced Reversible Transitions in Lipid-DNA Mesophases [J].
Danino, Dganit ;
Kesselman, Ellina ;
Saper, Gadiel ;
Petrache, Horia I. ;
Harries, Daniel .
BIOPHYSICAL JOURNAL, 2009, 96 (07) :L43-L45
[20]   Temperature-controlled poly(propylene) glycol hydrophobicity on the formation of inclusion complexes with modified cyclodextrins. A DSC and ITC study [J].
De Lisi, R. ;
Lazzara, G. ;
Milioto, S. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2011, 13 (27) :12571-12577