Biomimetic membrane systems to study cellular organization

2009 ◽  
Vol 168 (1) ◽  
pp. 143-151 ◽  
Author(s):  
Martin Loose ◽  
Petra Schwille
2014 ◽  
Vol 11 (96) ◽  
pp. 20140232 ◽  
Author(s):  
Bernhard Schuster ◽  
Uwe B. Sleytr

Designing and utilization of biomimetic membrane systems generated by bottom-up processes is a rapidly growing scientific and engineering field. Elucidation of the supramolecular construction principle of archaeal cell envelopes composed of S-layer stabilized lipid membranes led to new strategies for generating highly stable functional lipid membranes at meso- and macroscopic scale. In this review, we provide a state-of-the-art survey of how S-layer proteins, lipids and polymers may be used as basic building blocks for the assembly of S-layer-supported lipid membranes. These biomimetic membrane systems are distinguished by a nanopatterned fluidity, enhanced stability and longevity and, thus, provide a dedicated reconstitution matrix for membrane-active peptides and transmembrane proteins. Exciting areas in the (lab-on-a-) biochip technology are combining composite S-layer membrane systems involving specific membrane functions with the silicon world. Thus, it might become possible to create artificial noses or tongues, where many receptor proteins have to be exposed and read out simultaneously. Moreover, S-layer-coated liposomes and emulsomes copying virus envelopes constitute promising nanoformulations for the production of novel targeting, delivery, encapsulation and imaging systems.


2016 ◽  
Vol 46 (6) ◽  
pp. 546-551 ◽  
Author(s):  
Lavinia Liguori ◽  
Barry Stidder ◽  
Jean-Pierre Alcaraz ◽  
Jean-Luc Lenormand ◽  
Philippe Cinquin ◽  
...  

Author(s):  
Victoria Vitkova ◽  
Denitsa Mitkova ◽  
Vesela Yordanova ◽  
Peter Pohl ◽  
Udo Bakowsky ◽  
...  

Langmuir ◽  
2015 ◽  
Vol 31 (46) ◽  
pp. 12679-12687 ◽  
Author(s):  
Jacqueline J. Knobloch ◽  
Andrew R. J. Nelson ◽  
Ingo Köper ◽  
Michael James ◽  
Duncan J. McGillivray

Author(s):  
C. Wiencke ◽  
A. Lauchli

Osmoregulatory mechanisms in algae were investigated mainly from a physiological point of view (KAUSS 1977, HELLEBUST 1976). In Porphyra two osmotic agents, i. e. floridoside/isofloridoside (KAUSS 1968) and certain ions, such as K+ and Na+(EPPLEY et al. 1960) are considered for osmotic balance. Accumulations of ions (particularly Na+) in the cytoplasm during osmotic adaptation is improbable, because the activity of enzymes is generally inhibited by high ionic concentrations (FLOWERS et al. 1977).The cellular organization of Porphyra was studied with special emphasis on the development of the vacuolar system under different hyperosmotic conditions. Porphyra was cultivated at various strengths of the culture medium ASP 12 (PROVASOLI 1961) ranging from normal to 6 times concentrated (6x) culture medium. Por electron microscopy freeze fracturing was used (specimens fixed in 2% glutaraldehyde and incubated in 30% glycerol, preparation in a BALZERS BA 360 M apparatus), because chemical fixation gave poor results.


Author(s):  
Robert M. Glaeser ◽  
David W. Deamer

In the investigation of the molecular organization of cell membranes it is often supposed that lipid molecules are arranged in a bimolecular film. X-ray diffraction data obtained in a direction perpendicular to the plane of suitably layered membrane systems have generally been interpreted in accord with such a model of the membrane structure. The present studies were begun in order to determine whether selected area electron diffraction would provide a tool of sufficient sensitivity to permit investigation of the degree of intermolecular order within lipid films. The ultimate objective would then be to apply the method to single fragments of cell membrane material in order to obtain data complementary to the transverse data obtainable by x-ray diffraction.


Author(s):  
J. K. Samarabandu ◽  
R. Acharya ◽  
D. R. Pareddy ◽  
P. C. Cheng

In the study of cell organization in a maize meristem, direct viewing of confocal optical sections in 3D (by means of 3D projection of the volumetric data set, Figure 1) becomes very difficult and confusing because of the large number of nucleus involved. Numerical description of the cellular organization (e.g. position, size and orientation of each structure) and computer graphic presentation are some of the solutions to effectively study the structure of such a complex system. An attempt at data-reduction by means of manually contouring cell nucleus in 3D was reported (Summers et al., 1990). Apart from being labour intensive, this 3D digitization technique suffers from the inaccuracies of manual 3D tracing related to the depth perception of the operator. However, it does demonstrate that reducing stack of confocal images to a 3D graphic representation helps to visualize and analyze complex tissues (Figure 2). This procedure also significantly reduce computational burden in an interactive operation.


2014 ◽  
Vol 62 (S 01) ◽  
Author(s):  
S. Dhein ◽  
A. Schreiber ◽  
S. Steinbach ◽  
M. Kostelka ◽  
F.W. Mohr

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