scholarly journals What are the true values of the bending modulus of simple lipid bilayers?

2015 ◽  
Vol 185 ◽  
pp. 3-10 ◽  
Author(s):  
John F. Nagle ◽  
Michael S. Jablin ◽  
Stephanie Tristram-Nagle ◽  
Kiyotaka Akabori
Soft Matter ◽  
2021 ◽  
Author(s):  
Ryan W. Loney ◽  
Bret Brandner ◽  
Maayan P. Dagan ◽  
Paige N. Smith ◽  
Megan Roche ◽  
...  

We used X-ray diffuse scattering to determine the bending modulus of lipid bilayers and an order parameter of the acyl chains to establish how the hydrophobic surfactant proteins, SP-B and SP-C, promote adsorption of lipids to an air/water interface.


2016 ◽  
Vol 196 ◽  
pp. 76-80 ◽  
Author(s):  
John F. Nagle ◽  
Michael S. Jablin ◽  
Stephanie Tristram-Nagle
Keyword(s):  

2018 ◽  
Vol 97 (3) ◽  
Author(s):  
Adarsh K. Chaurasia ◽  
Andrew M. Rukangu ◽  
Michael K. Philen ◽  
Gary D. Seidel ◽  
Eric C. Freeman

Membranes ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 533
Author(s):  
Jeel Raval ◽  
Ekaterina Gongadze ◽  
Metka Benčina ◽  
Ita Junkar ◽  
Niharika Rawat ◽  
...  

In this review paper, we theoretically explain the origin of electrostatic interactions between lipid bilayers and charged solid surfaces using a statistical mechanics approach, where the orientational degree of freedom of lipid head groups and the orientational ordering of the water dipoles are considered. Within the modified Langevin Poisson–Boltzmann model of an electric double layer, we derived an analytical expression for the osmotic pressure between the planar zwitterionic lipid bilayer and charged solid planar surface. We also show that the electrostatic interaction between the zwitterionic lipid head groups of the proximal leaflet and the negatively charged solid surface is accompanied with a more perpendicular average orientation of the lipid head-groups. We further highlight the important role of the surfaces’ nanostructured topography in their interactions with biological material. As an example of nanostructured surfaces, we describe the synthesis of TiO2 nanotubular and octahedral surfaces by using the electrochemical anodization method and hydrothermal method, respectively. The physical and chemical properties of these nanostructured surfaces are described in order to elucidate the influence of the surface topography and other physical properties on the behavior of human cells adhered to TiO2 nanostructured surfaces. In the last part of the paper, we theoretically explain the interplay of elastic and adhesive contributions to the adsorption of lipid vesicles on the solid surfaces. We show the numerically predicted shapes of adhered lipid vesicles corresponding to the minimum of the membrane free energy to describe the influence of the vesicle size, bending modulus, and adhesion strength on the adhesion of lipid vesicles on solid charged surfaces.


2021 ◽  
Vol 22 (12) ◽  
pp. 6547
Author(s):  
Luka Šturm ◽  
Nataša Poklar Ulrih

Studying the interactions between lipid membranes and various bioactive molecules (e.g., polyphenols) is important for determining the effects they can have on the functionality of lipid bilayers. This knowledge allows us to use the chosen compounds as potential inhibitors of bacterial and cancer cells, for elimination of viruses, or simply for keeping our healthy cells in good condition. As studying those effect can be exceedingly difficult on living cells, model lipid membranes, such as liposomes, can be used instead. Liposomal bilayer systems represent the most basic platform for studying those interactions, as they are simple, quite easy to prepare and relatively stable. They are especially useful for investigating the effects of bioactive compounds on the structure and kinetics of simple lipid membranes. In this review, we have described the most basic methods available for preparation of liposomes, as well as the essential techniques for studying the effects of bioactive compounds on those liposomes. Additionally, we have provided details for an easy laboratory implementation of some of the described methods, which should prove useful especially to those relatively new on this research field.


2017 ◽  
Vol 19 (41) ◽  
pp. 27930-27934 ◽  
Author(s):  
Bruno C. Borro ◽  
Lucia Parolini ◽  
Pietro Cicuta ◽  
Vito Foderà ◽  
Lorenzo Di Michele

Prefibrillar species cause a significant reduction in the bending modulus of lipid bilayers, without large-scale morphological disruption.


Author(s):  
Neng-Bo He ◽  
S.W. Hui

Monolayers and planar "black" lipid membranes have been widely used as models for studying the structure and properties of biological membranes. Because of the lack of a suitable method to prepare these membranes for electron microscopic observation, their ultrastructure is so far not well understood. A method of forming molecular bilayers over the holes of fine mesh grids was developed by Hui et al. to study hydrated and unsupported lipid bilayers by electron diffraction, and to image phase separated domains by diffraction contrast. We now adapted the method of Pattus et al. of spreading biological membranes vesicles on the air-water interfaces to reconstitute biological membranes into unsupported planar films for electron microscopic study. hemoglobin-free human erythrocyte membrane stroma was prepared by hemolysis. The membranes were spreaded at 20°C on balanced salt solution in a Langmuir trough until a surface pressure of 20 dyne/cm was reached. The surface film was repeatedly washed by passing to adjacent troughs over shallow partitions (fig. 1).


Author(s):  
S. Kirchanski ◽  
D. Branton

We have investigated the effect of integral membrane proteins upon the fracturing of frozen lipid bilayers. This investigation has been part of an effort to develop freeze fracture labeling techniques and to assess the possible breakage of covalent protein bonds during the freeze fracture process. We have developed an experimental protocol utilizing lectin affinity columns which should detect small amounts of covalent bond breakage during the fracture of liposomes containing purified (1) glycophorin (a transmembrane glycoprotein of human erythrocyte membranes). To fracture liposomes in bulk, frozen liposomes are ground repeatedly under liquid nitrogen. Failure to detect any significant covalent bond breakage (contrary to (2)) led us to question the effectiveness of our grinding procedure in fracturing and splitting lipid bilayers.


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