scholarly journals A pressure-jump study on the interaction of osmolytes and crowders with cubic monoolein structures

Soft Matter ◽  
2022 ◽  
Author(s):  
Göran Surmeier ◽  
Michael Paulus ◽  
Eric Schneider ◽  
Susanne Dogan ◽  
Metin Tolan ◽  
...  

Cellular solutes affect the equilibration of cubic lipid structures after pressure-induced phase transitions.

Soft Matter ◽  
2011 ◽  
Vol 7 (6) ◽  
pp. 2709 ◽  
Author(s):  
Christoph Jeworrek ◽  
Sebastian Uelner ◽  
Roland Winter

2014 ◽  
Vol 228 (10-12) ◽  
Author(s):  
Nicholas J. Brooks ◽  
John M. Seddon

AbstractHydrostatic pressure has dramatic effects on biomembrane structure and stability and is a key thermodynamic parameter in the context of the biology of deep sea organisms. Furthermore, high-pressure and pressure-jump studies are very useful tools in biophysics and biotechnology, where they can be used to study the mechanism and kinetics of lipid phase transitions, biomolecular transformations, and protein folding/unfolding. Here, we first give an overview of the technology currently available for X-ray scattering studies of soft matter systems under pressure. We then illustrate the use of this technology to study a variety of lipid membrane systems.


2014 ◽  
Vol 70 (a1) ◽  
pp. C1187-C1187
Author(s):  
Oscar Ces ◽  
John Seddon ◽  
Robert Law ◽  
Nicholas Brooks ◽  
Richard Templer

When mixed with water, biological amphiphiles such as phospholipids can self-assemble to form a variety of lyotropic liquid crystalline structures including 1-D flat lamellar bilayers, 2-D hexagonal phases and 3-D bicontinuous cubic structures1. The role of the lamellar phase in nature is well understood – flat bilayers maintain the fundamental integrity of all living cells. However, non-lamellar phases also play a vital role in vivo. Extended cubic phases have been directly observed in cells and in addition, the repeating pores which form the continuously accessible structure of these bicontinuous phases are very closely structurally related to membrane pores formed during membrane fusion and fission. The equilibrium phase behaviour of pure phospholipids in water and simple model membrane mixtures has been widely studied but their out of equilibrium behaviour remains poorly understood. We have addressed this knowledge gap through pioneering work looking at the kinetics of phase transitions in phospholipid/water systems and phospholipid/protein/water mixtures using the pressure jump relaxation technique in conjunction with high speed, time resolved small angle X-ray diffraction. This presentation will provide an overview of how our bottom-up approach using model membrane systems has enabled us to establish the mechanistic routes and intermediates in a number of phase transition schemes including bicontinuous cubic to lamellar, hexagonal to lamellar and inter-cubic phase transitions.


2008 ◽  
Vol 64 (a1) ◽  
pp. C53-C53
Author(s):  
O. Ces ◽  
N.J. Brooks ◽  
J.M. Seddon ◽  
R. Winter ◽  
C. Conn ◽  
...  

Author(s):  
John M Seddon ◽  
Adam M Squires ◽  
Charlotte E Conn ◽  
Oscar Ces ◽  
Andrew J Heron ◽  
...  

In this paper, we give an overview of our studies by static and time-resolved X-ray diffraction of inverse cubic phases and phase transitions in lipids. In §1 , we briefly discuss the lyotropic phase behaviour of lipids, focusing attention on non-lamellar structures, and their geometric/topological relationship to fusion processes in lipid membranes. Possible pathways for transitions between different cubic phases are also outlined. In §2 , we discuss the effects of hydrostatic pressure on lipid membranes and lipid phase transitions, and describe how the parameters required to predict the pressure dependence of lipid phase transition temperatures can be conveniently measured. We review some earlier results of inverse bicontinuous cubic phases from our laboratory, showing effects such as pressure-induced formation and swelling. In §3 , we describe the technique of pressure-jump synchrotron X-ray diffraction. We present results that have been obtained from the lipid system 1 : 2 dilauroylphosphatidylcholine/lauric acid for cubic–inverse hexagonal, cubic–cubic and lamellar–cubic transitions. The rate of transition was found to increase with the amplitude of the pressure-jump and with increasing temperature. Evidence for intermediate structures occurring transiently during the transitions was also obtained. In §4 , we describe an IDL-based ‘ AXcess ’ software package being developed in our laboratory to permit batch processing and analysis of the large X-ray datasets produced by pressure-jump synchrotron experiments. In §5 , we present some recent results on the fluid lamellar– Pn 3 m cubic phase transition of the single-chain lipid 1-monoelaidin, which we have studied both by pressure-jump and temperature-jump X-ray diffraction. Finally, in §6 , we give a few indicators of future directions of this research. We anticipate that the most useful technical advance will be the development of pressure-jump apparatus on the microsecond time-scale, which will involve the use of a stack of piezoelectric pressure actuators. The pressure-jump technique is not restricted to lipid phase transitions, but can be used to study a wide range of soft matter transitions, ranging from protein unfolding and DNA unwinding and transitions, to phase transitions in thermotropic liquid crystals, surfactants and block copolymers.


Author(s):  
G. Timp ◽  
L. Salamanca-Riba ◽  
L.W. Hobbs ◽  
G. Dresselhaus ◽  
M.S. Dresselhaus

Electron microscopy can be used to study structures and phase transitions occurring in graphite intercalations compounds. The fundamental symmetry in graphite intercalation compounds is the staging periodicity whereby each intercalate layer is separated by n graphite layers, n denoting the stage index. The currently accepted model for intercalation proposed by Herold and Daumas assumes that the sample contains equal amounts of intercalant between any two graphite layers and staged regions are confined to domains. Specifically, in a stage 2 compound, the Herold-Daumas domain wall model predicts a pleated lattice plane structure.


Author(s):  
James F. Hainfeld

Lipids are an important class of molecules, being found in membranes, HDL, LDL, and other natural structures, serving essential roles in structure and with varied functions such as compartmentalization and transport. Synthetic liposomes are also widely used as delivery and release vehicles for drugs, cosmetics, and other chemicals; soap is made from lipids. Lipids may form bilayer or multilammellar vesicles, micelles, sheets, tubes, and other structures. Lipid molecules may be linked to proteins, carbohydrates, or other moieties. EM study of this essential ingredient of life has lagged, due to lack of direct methods to visualize lipids without extensive alteration. OsO4 reacts with double bonds in membrane phospholipids, forming crossbridges. This has been the method of choice to both fix and stain membranes, thus far. An earlier work described the use of tungstate clusters (W11) attached to lipid moieties to form lipid structures and lipid probes.


Author(s):  
Oleg Bostanjoglo ◽  
Peter Thomsen-Schmidt

Thin GexTe1-x (x = 0.15-0.8) were studied as a model substance of a composite semiconductor film, in addition being of interest for optical storage material. Two complementary modes of time-resolved TEM were used to trace the phase transitions, induced by an attached Q-switched (50 ns FWHM) and frequency doubled (532 nm) Nd:YAG laser. The laser radiation was focused onto the specimen within the TEM to a 20 μm spot (FWHM). Discrete intermediate states were visualized by short-exposure time doubleframe imaging /1,2/. The full history of a transformation was gained by tracking the electron image intensity with photomultiplier and storage oscilloscopes (space/time resolution 100 nm/3 ns) /3/. In order to avoid radiation damage by the probing electron beam to detector and specimen, the beam is pulsed in this continuous mode of time-resolved TEM,too.Short events ( <2 μs) are followed by illuminating with an extended single electron pulse (fig. 1c)


Author(s):  
Rohan Abeyaratne ◽  
James K. Knowles
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