Cationic liposome-microtubule complexes: Pathways to the formation of two-state lipid-protein nanotubes with open or closed ends

被引:85
作者
Raviv, U [1 ]
Needleman, DJ
Li, YL
Miller, HP
Wilson, L
Safinya, CR
机构
[1] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Phys, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
[4] Univ Calif Santa Barbara, Biomol Sci & Engn Program, Santa Barbara, CA 93106 USA
关键词
polyelectrolyte lipid complexes; small angle x-ray scattering; nanotube-based drug delivery; membrane; tubulin;
D O I
10.1073/pnas.0502183102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Intermolecular interactions between charged membranes and biological polyelectrolytes, tuned by physical parameters, which include the membrane charge density and bending rigidity, the membrane spontaneous curvature, the biopolymer curvature, and the overall charge of the complex, lead to distinct structures and morphologies. The self-assembly of cationic liposome-microtubule (MT) complexes was studied, using synchrotron x-ray scattering and electron microscopy. Vesicles were found to either adsorb onto MTs, forming a "beads on a rod" structure, or undergo a wetting transition and coating the MT. Tubulin oligomers then coat the external lipid layer, forming a tunable lipid-protein nanotube. The beads on a rod structure is a kinetically trapped state. The energy barrier between the states depends on the membrane bending rigidity and charge density. By controlling the cationic lipid/tubulin stoichiometry it is possible to switch between two states of nanotubes with either open ends or closed ends with lipid caps, a process that forms the basis for controlled chemical and drug encapsulation and release.
引用
收藏
页码:11167 / 11172
页数:6
相关论文
共 42 条
[1]   LOW RESOLUTION STRUCTURE OF MICROTUBULES IN SOLUTION - SYNCHROTRON X-RAY-SCATTERING AND ELECTRON-MICROSCOPY OF TAXOL-INDUCED MICROTUBULES ASSEMBLED FROM PURIFIED TUBULIN IN COMPARISON WITH GLYCEROL AND MAP-INDUCED MICROTUBULES [J].
ANDREU, JM ;
BORDAS, J ;
DIAZ, JF ;
DEANCOS, JG ;
GIL, R ;
MEDRANO, FJ ;
NOGALES, E ;
PANTOS, E ;
TOWNSANDREWS, E .
JOURNAL OF MOLECULAR BIOLOGY, 1992, 226 (01) :169-184
[2]   Observation of a rectangular columnar phase in condensed lamellar cationic lipid-DNA complexes [J].
Artzner, F ;
Zantl, R ;
Rapp, G ;
Radler, JO .
PHYSICAL REVIEW LETTERS, 1998, 81 (22) :5015-5018
[3]  
CHAUDHURI A, 2003, CURR MED CHEM, V10, P1185
[4]   A PHASE OF LIPOSOMES WITH ENTANGLED TUBULAR VESICLES [J].
CHIRUVOLU, S ;
WARRINER, HE ;
NARANJO, E ;
IDZIAK, SHJ ;
RADLER, JO ;
PLANO, RJ ;
ZASADZINSKI, JA ;
SAFINYA, CR .
SCIENCE, 1994, 266 (5188) :1222-1225
[5]   Intracytoplasmic delivery of anionic proteins [J].
Dalkara, D ;
Zuber, G ;
Behr, JP .
MOLECULAR THERAPY, 2004, 9 (06) :964-969
[6]   The structure of DNA complexes with cationic liposomes - cylindrical or flat bilayers? [J].
Dan, N .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1998, 1369 (01) :34-38
[7]   POLYCATION-INDUCED ASSEMBLY OF PURIFIED TUBULIN [J].
ERICKSON, HP ;
VOTER, WA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (08) :2813-2817
[8]   Cationic lipid-DNA complexes for gene therapy: Understanding the relationship between complex structure and gene delivery pathways at the molecular level [J].
Ewert, K ;
Slack, NL ;
Ahmad, A ;
Evans, HM ;
Lin, AJ ;
Samuel, CE ;
Safinya, CR .
CURRENT MEDICINAL CHEMISTRY, 2004, 11 (02) :133-149
[9]   TUBULIN COLCHICINE COMPLEXES DIFFERENTIALLY POISON OPPOSITE MICROTUBULE ENDS [J].
FARRELL, KW ;
WILSON, L .
BIOCHEMISTRY, 1984, 23 (16) :3741-3748
[10]  
FEIGNER PL, 1987, P NATL ACAD SCI USA, V84, P7413, DOI DOI 10.1073/PNAS.84.21.7413