Single-Chain Polyprenyl Phosphates Form“Primitive” Membranes

1996 ◽  
Vol 35 (2) ◽  
pp. 177-180 ◽  
Author(s):  
Gianluca Pozzi ◽  
Véronique Birault ◽  
Birgit Werner ◽  
Olivier Dannenmuller ◽  
Yoichi Nakatani ◽  
...  
Keyword(s):  
Single Chain ◽  
Polyprenyl Phosphates ◽  
Primitive Membranes

Sodium di-polyprenyl phosphates form “primitive” membranes

1992 ◽  
Vol 33 (36) ◽  
pp. 5249-5252 ◽  
Author(s):  
Niklas Plobeck ◽  
Stéphane Eifler ◽  
Alain Brisson ◽  
Yoichi Nakatani ◽  
Guy Ourisson
Keyword(s):  
Polyprenyl Phosphates ◽  
Primitive Membranes

Monolayer Studies of Single-Chain Polyprenyl Phosphates

Langmuir ◽  
2005 ◽  
Vol 21 (10) ◽  
pp. 4578-4583 ◽  
Author(s):  
Katsuhiko Ariga ◽  
Harufumi Yuki ◽  
Jun-ichi Kikuchi ◽  
Olivier Dannemuller ◽  
Anne-Marie Albrecht-Gary ◽  
...  
Keyword(s):  
Single Chain ◽  
Polyprenyl Phosphates

Reinforcing effect of bi- and tri-cyclopolyprenols on ‘primitive’ membranes made of polyprenyl phosphates

Tetrahedron ◽  
2007 ◽  
Vol 63 (16) ◽  
pp. 3395-3407 ◽  
Author(s):  
Nigel Ribeiro ◽  
Stéphane Streiff ◽  
Denis Heissler ◽  
Mourad Elhabiri ◽  
Anne Marie Albrecht-Gary ◽  
...  
Keyword(s):  
Reinforcing Effect ◽  
Polyprenyl Phosphates ◽  
Primitive Membranes

scholarly journals Search for the Most ‘primitive’ Membranes and Their Reinforcers: A Review of the Polyprenyl Phosphates Theory

2014 ◽  
Vol 44 (3) ◽  
pp. 197-208 ◽  
Author(s):  
Yoichi Nakatani ◽  
Nigel Ribeiro ◽  
Stéphane Streiff ◽  
Mari Gotoh ◽  
Gianluca Pozzi ◽  
...  
Keyword(s):  
Polyprenyl Phosphates ◽  
Primitive Membranes

Cryo-electron microscopy of two-dimensional crystals of reduced type B botulinum neurotoxin

1992 ◽  
Vol 50 (1) ◽  
pp. 530-531
Author(s):  
P. F. Flicker ◽  
V.S. Kulkarni ◽  
J. P. Robinson ◽  
G. Stubbs ◽  
B. R. DasGupta
Keyword(s):  
Disulfide Bonds ◽  
Clostridium Botulinum ◽  
Structural Changes ◽  
Two Dimensional ◽  
Type B ◽  
Single Chain ◽  
Muscle Paralysis ◽  
Cryo Electron Microscopy ◽  
Disulfide Linkages ◽  
Intracellular Action

Botulinum toxin is a potent neurotoxin produced by Clostridium botulinum. The toxin inhibits release of neurotransmitter, causing muscle paralysis. There are several serotypes, A to G, all of molecular weight about 150,000. The protein exists as a single chain or or as two chains, with two disulfide linkages. In a recent investigation on intracellular action of neurotoxins it was reported that type B neurotoxin can inhibit the release of Ca++-activated [3H] norepinephrine only if the disulfide bonds are reduced. In order to investigate possible structural changes in the toxin upon reduction of the disulfide bonds, we have prepared two-dimensional crystals of reduced type B neurotoxin. These two-dimensional crystals will be compared with those of the native (unreduced) type B toxin.

Fine structure and properties of defects in naturally occurring silicates and oxides

1990 ◽  
Vol 48 (4) ◽  
pp. 460-461
Author(s):  
David R. Veblen
Keyword(s):  
Chemical Reactions ◽  
High Resolution Electron Microscopy ◽  
Extended Defects ◽  
Single Chain ◽  
Naturally Occurring ◽  
Resolution Electron ◽  
Fine Structures ◽  
Image Simulations ◽  
Similar Crystal Structure

Extended defects and interfaces control many processes in rock-forming minerals, from chemical reactions to rock deformation. In many cases, it is not the average structure of a defect or interface that is most important, but rather the structure of defect terminations or offsets in an interface. One of the major thrusts of high-resolution electron microscopy in the earth sciences has been to identify the role of defect fine structures in reactions and to determine the structures of such features. This paper will review studies using HREM and image simulations to determine the structures of defects in silicate and oxide minerals and present several examples of the role of defects in mineral chemical reactions. In some cases, the geological occurrence can be used to constrain the diffusional properties of defects.The simplest reactions in minerals involve exsolution (precipitation) of one mineral from another with a similar crystal structure, and pyroxenes (single-chain silicates) provide a good example. Although conventional TEM studies have led to a basic understanding of this sort of phase separation in pyroxenes via spinodal decomposition or nucleation and growth, HREM has provided a much more detailed appreciation of the processes involved.

Elemental mass loss in silicate minerals during x-ray analysis

1990 ◽  
Vol 48 (4) ◽  
pp. 804-805
Author(s):  
P.E. Champness ◽  
R.W. Devenish
Keyword(s):  
Mass Loss ◽  
Current Density ◽  
Damage Mechanism ◽  
Beam Current ◽  
Single Chain ◽  
Plagioclase Feldspar ◽  
X Ray ◽  
Alkali Ions ◽  
Structural Order ◽  
Sheet Silicate

It has long been recognised that silicates can suffer extensive beam damage in electron-beam instruments. The predominant damage mechanism is radiolysis. For instance, damage in quartz, SiO2, results in loss of structural order without mass loss whereas feldspars (framework silicates containing Ca, Na, K) suffer loss of structural order with accompanying mass loss. In the latter case, the alkali ions, particularly Na, are found to migrate away from the area of the beam. The aim of the present study was to investigate the loss of various elements from the common silicate structures during electron irradiation at 100 kV over a range of current densities of 104 - 109 A m−2. (The current density is defined in terms of 50% of total current in the FWHM probe). The silicates so far ivestigated are:- olivine [(Mg, Fe)SiO4], a structure that has isolated Si-O tetrahedra, garnet [(Mg, Ca, Fe)3Al2Si3AO12 another silicate with isolated tetrahedra, pyroxene [-Ca(Mg, Fe)Si2O6 a single-chain silicate; mica [margarite, -Ca2Al4Si4Al4O2O(OH)4], a sheet silicate, and plagioclase feldspar [-NaCaAl3Si5O16]. Ion- thinned samples of each mineral were examined in a VG Microscopes UHV HB501 field- emission STEM. The beam current used was typically - 0.5 nA and the current density was varied by defocussing the electron probe. Energy-dispersive X-ray spectra were collected every 10 seconds for a total of 200 seconds using a Link Systems windowless detector. The thickness of the samples in the area of analysis was normally 50-150 nm.

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