TY - JOUR
T1 - Cationic liposome-microtubule complexes
T2 - Pathways to the formation of two-state lipid-protein nanotubes with open or closed ends
AU - Raviv, Uri
AU - Needleman, Daniel J.
AU - Li, Youli
AU - Miller, Herbert P.
AU - Wilson, Leslie
AU - Safinya, Cyrus R.
PY - 2005/8/9
Y1 - 2005/8/9
N2 - 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.
AB - 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.
KW - Membrane
KW - Nanotube-based drug delivery
KW - Polyelectrolyte lipid complexes
KW - Small angle x-ray scattering
KW - Tubulin
UR - http://www.scopus.com/inward/record.url?scp=23844479241&partnerID=8YFLogxK
U2 - 10.1073/pnas.0502183102
DO - 10.1073/pnas.0502183102
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C2 - 16055561
AN - SCOPUS:23844479241
SN - 0027-8424
VL - 102
SP - 11167
EP - 11172
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 32
ER -