A. Leitmannova Liu's Advances in Planar Lipid Bilayers and Liposomes, Vol. 10 PDF

By A. Leitmannova Liu

Advances in Planar Lipid Bilayers and Liposomes, Volume 10, maintains to incorporate invited chapters on a extensive diversity of themes, overlaying either major preparations of the reconstituted approach, specifically planar lipid bilayers and round liposomes. The invited authors current the most recent ends up in this fascinating multidisciplinary box in their personal examine group.
Many of the members operating in either fields over many many years have been in shut collaboration with the overdue Prof. H. Ti Tien, the founding editor of this publication sequence. There also are chapters written by means of the various more youthful iteration of scientists incorporated during this sequence. This quantity retains in brain the wider objective with either structures, planar lipid bilayers and round liposomes, that is the additional improvement of this interdisciplinary box world wide.
* contains contributions from rookies and verified and skilled researchers
* Explores the planar lipid bilayer platforms and round liposomes from either theoretical and experimental perspectives
* Serves as an integral resource of data for brand new scientists

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This process depends on the local curvature of the membrane, which is—in turn—determined by the local composition of its constituents, their intrinsic shape and interactions with the neighboring molecules (see also Section 3, Fig. 25). In favor of this assumption is that the tips of the nanotubes tend to accumulate ganglioside GM1 (Fig. 19) as one of the characteristic components of membrane nanodomains referred to as membrane rafts. Membrane rafts are small (10–200 nm), heterogeneous, highly dynamic, sterol- and sphingolipid-enriched domains that compartmentalize cellular processes.

Prior to fusion of the gondola with the target cell membrane, no neck formation is needed (Fig. 17C) since the neck is already part of the nanotube connecting the gondola to the membrane of the target cell. This is contrary to the case of a free transport vesicle. It can therefore be concluded that the transport of material in dilatations (or the transport of molecules composing the membrane of dilatations) may be more efficient, since it is guided either by actomyosin transport system or passive diffusion along the nanotube, and therefore energetically advantageous over free vesicle transport.

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