Phase behaviour of parallel hard rods in confinement: an Onsager theory study

2010 ◽  
Vol 22 (17) ◽  
pp. 175002 ◽  
Author(s):  
Alexandr Malijevský ◽  
Szabolcs Varga
2014 ◽  
Vol 141 (15) ◽  
pp. 154903 ◽  
Author(s):  
Thomas Troppenz ◽  
Laura Filion ◽  
René van Roij ◽  
Marjolein Dijkstra

Author(s):  
K. Slyusarenko ◽  
V. Reshetnyak ◽  
Yu. Reznikov

The Onsager theory of hard rod dispersion in a neutral solvent is extended to a case of two-component dispersion consisting of both non-magnetic and magnetic rods. It was found that the alignment of magneto-sensitive dispersion component by a magnetic field leads to the alignment of non-magnetic component in the dispersion and to an elimination of the isotropic phase. This effect is significant even at low relative concentrations of magnetic rods and leads to a magnetically induced anisotropy in a non-magnetic dispersion of rods mixed with the magnetic ones.


1996 ◽  
Vol 105 (17) ◽  
pp. 7727-7734 ◽  
Author(s):  
Richard P. Sear ◽  
Bela M. Mulder

Author(s):  
D. Chrétien ◽  
D. Job ◽  
R.H. Wade

Microtubules are filamentary structures found in the cytoplasm of eukaryotic cells, where, together with actin and intermediate filaments, they form the components of the cytoskeleton. They have many functions and show various levels of structural complexity as witnessed by the singlet, doublet and triplet structures involved in the architecture of centrioles, basal bodies, cilia and flagella. The accepted microtubule model consists of a 25 nm diameter hollow tube with a wall made up of 13 paraxial protofilaments (pf). Each pf is a string of aligned tubulin dimers. Some results have suggested that the pfs follow a superhelix. To understand how microtubules function in the cell an accurate model of the surface lattice is one of the requirements. For example the 9x2 architecture of the axoneme will depend on the organisation of its component microtubules. We should also note that microtubules with different numbers of pfs have been observed in thin sections of cellular and of in-vitro material. An outstanding question is how does the surface lattice adjust to these different pf numbers?We have been using cryo-electron microscopy of frozen-hydrated samples to study in-vitro assembled microtubules. The experimental conditions are described in detail in this reference. The results obtained in conjunction with thin sections of similar specimens and with axoneme outer doublet fragments have already allowed us to characterise the image contrast of 13, 14 and 15 pf microtubules on the basis of the measured image widths, of the the image contrast symmetry and of the amplitude and phase behaviour along the equator in the computed Fourier transforms. The contrast variations along individual microtubule images can be interpreted in terms of the geometry of the microtubule surface lattice. We can extend these results and make some reasonable predictions about the probable surface lattices in the case of other pf numbers, see Table 1. Figure 1 shows observed images with which these predictions can be compared.


2008 ◽  
Vol 59 (11) ◽  
Author(s):  
Maria Tomoaia-Cotisel ◽  
Aurora Mocanu

The phase behaviour and surface structure of dipalmitoyl phosphatidyl choline (DPPC) monolayers at the air/water interface, in the absence and the presence of procaine, have been investigated by Langmuir-Blodgett (LB) technique and atomic force microscopy. The LB films were transferred on mica, at a controlled surface pressure, characteristic for the expanded liquid to condensed liquid phase transition of pure DPPC monolayers. The results indicate that procaine penetrates into and specifically interacts with phospholipid monolayers stabilizing the lipid membrane interface.


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