On the Ability of PAMAM Dendrimers and Dendrimer/DNA Aggregates To Penetrate POPC Model Biomembranes

被引:51
作者
Ainalem, Marie-Louise [1 ]
Campbell, Richard A. [2 ]
Khalid, Syma [3 ]
Gillams, Richard J. [3 ]
Rennie, Adrian R. [4 ]
Nylander, Tommy [1 ]
机构
[1] Lund Univ, Ctr Chem & Chem Engn, S-22100 Lund, Sweden
[2] Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
[3] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England
[4] Uppsala Univ, Dept Phys, S-75121 Uppsala, Sweden
基金
瑞典研究理事会;
关键词
MOLECULAR-DYNAMICS SIMULATIONS; POLYMER-CUSHIONED BILAYERS; SOLID-LIQUID INTERFACE; COARSE-GRAINED MODEL; LIPID-BILAYERS; POLY(AMIDOAMINE) DENDRIMERS; LIGHT-SCATTERING; POLYAMIDOAMINE DENDRIMERS; NEUTRON REFLECTIVITY; GENE DELIVERY;
D O I
10.1021/jp9119809
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
Poly(amido amine) (PAMAM) dendrimers have previously been shown, as cationic condensing agents of DNA, to have high potential for nonviral gene delivery. This study addresses two key issues for gene delivery: the interaction of the biomembrane with (i) the condensing agent (the cationic PAMAM dendrimer) and (ii) the corresponding dendrimer/DNA aggregate. Using in situ null ellipsometry and neutron reflection, parallel experiments were carried out involving dendrimers or generations 2 (G2), 4 (G4), and 6 (G6). The study demonstrates that free dendrimers of all three generations were able to traverse supported palmitoyloleoylphosphatidylcholine (POPC) bilayers deposited on silica surfaces. The model biomembranes were elevated front the solid surfaces upon dendrimer penetration, which offers a promising new way to generate more realistic model biomembranes where the contact with the supporting surface is reduced and where aqueous cavities are present beneath the bilayer. The largest dendrimer (GO) induced partial bilayer destruction directly upon penetration, whereas the smaller dendrimers (G2 and G4) leave the bilayer intact, so we propose that lower generation dendrimers have greater potential as transfection mediators. In addition to the experimental observations, coarse-grained simulations on the interaction between generation 3 (03) dendrimers and POPC bilayers were performed in the absence and presence of a bilayer-supporting negatively charged surface that emulates the support. The simulations demonstrate that G3 is transported across free-standing POPC bilayers by direct penetration and not by endocytosis. The penetrability was, however, reduced in the presence of a surface, indicating that the membrane transport observed experimentally was not driven solely by the surface. The experimental reflection techniques were also applied to dendrimer/DNA aggregates of charge ratio = 0.5, and while G2/DNA and G4/DNA aggregates interact with POPC bilayers. G6/DNA displays no such interaction. These results indicate that, in contrast to free dendrimer molecules, dendrimer/DNA aggregates of low charge ratios are not able to traverse a membrane by direct penetration.
引用
收藏
页码:7229 / 7244
页数:16
相关论文
共 79 条
[21]   Interactions of poly(amidoamine) dendrimers with Survanta lung surfactant: The importance of lipid domains [J].
Erickson, Blake ;
DiMaggio, Stassi C. ;
Mullen, Douglas G. ;
Kelly, Christopher V. ;
Leroueil, Pascale R. ;
Berry, Stephanie A. ;
Baker, James R., Jr. ;
Orr, Bradford G. ;
Holl, Mark M. Banaszak .
LANGMUIR, 2008, 24 (19) :11003-11008
[22]   A SMOOTH PARTICLE MESH EWALD METHOD [J].
ESSMANN, U ;
PERERA, L ;
BERKOWITZ, ML ;
DARDEN, T ;
LEE, H ;
PEDERSEN, LG .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (19) :8577-8593
[23]   Stability of Asymmetric Lipid Bilayers Assessed by Molecular Dynamics Simulations [J].
Esteban-Martin, Santi ;
Risselada, H. Jelger ;
Salgado, Jesus ;
Marrink, Siewert J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (42) :15194-15202
[24]   A fluid floating bilayer [J].
Fragneto, G ;
Charitat, T ;
Graner, F ;
Mecke, K ;
Perino-Gallice, L ;
Bellet-Amalric, E .
EUROPHYSICS LETTERS, 2001, 53 (01) :100-106
[25]   A DSC and Raman spectroscopy study on the effect of PAMAM dendrimer on DPPC model lipid membranes [J].
Gardikis, Konstantinos ;
Hatziantoniou, Sophia ;
Viras, Kyriakos ;
Wagner, Matthias ;
Demetzos, Costas .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 318 (1-2) :118-123
[26]   Interaction of poly(amidoamine) dendrimers with supported lipid bilayers and cells: Hole formation and the relation to transport [J].
Hong, SP ;
Bielinska, AU ;
Mecke, A ;
Keszler, B ;
Beals, JL ;
Shi, XY ;
Balogh, L ;
Orr, BG ;
Baker, JR ;
Holl, MMB .
BIOCONJUGATE CHEMISTRY, 2004, 15 (04) :774-782
[27]   Floating lipid bilayers deposited on chemically grafted phosphatidylcholine surfaces [J].
Hughes, Arwel V. ;
Howse, Jonathan R. ;
Dabkowska, Aleksandra ;
Jones, Richard A. L. ;
Lawrence, M. Jayne ;
Roser, Stephen J. .
LANGMUIR, 2008, 24 (05) :1989-1999
[28]   VMD: Visual molecular dynamics [J].
Humphrey, W ;
Dalke, A ;
Schulten, K .
JOURNAL OF MOLECULAR GRAPHICS & MODELLING, 1996, 14 (01) :33-38
[29]   Transport of dendrimer nanocarriers through epithelial cells via the transcellular route [J].
Jevprasesphant, R ;
Penny, J ;
Attwood, D ;
D'Emanuele, A .
JOURNAL OF CONTROLLED RELEASE, 2004, 97 (02) :259-267
[30]   The influence of surface modification on the cytotoxicity of PAMAM dendrimers [J].
Jevprasesphant, R ;
Penny, J ;
Jalal, R ;
Attwood, D ;
McKeown, NB ;
D'Emanuele, A .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 252 (1-2) :263-266