Fine Particle 2D Crystals Prepared by the Dynamic Thin Laminar Flow Method†

Langmuir ◽  
1997 ◽  
Vol 13 (12) ◽  
pp. 3226-3234 ◽  
Author(s):  
Gilles Picard
Keyword(s):  
Laminar Flow ◽  
Fine Particle ◽  
Flow Method ◽  
2D Crystals

Device for monitoring sugar-solution concentration by a thermophysical laminar-flow method

1994 ◽  
Vol 37 (5) ◽  
pp. 585-589
Author(s):  
S. V. Ponomarev ◽  
S. V. Mishchenko ◽  
V. M. Zhilkin ◽  
A. V. Sinel'nikov
Keyword(s):  
Laminar Flow ◽  
Solution Concentration ◽  
Sugar Solution ◽  
Flow Method

Re-evaluation of the Pressure Effect for Nucleation in Laminar Flow Diffusion Chamber Experiments with Fluent and the Fine Particle Model

2009 ◽  
Vol 113 (8) ◽  
pp. 1434-1439 ◽  
Author(s):  
E. Herrmann ◽  
A.-P. Hyvärinen ◽  
D. Brus ◽  
H. Lihavainen ◽  
M. Kulmala
Keyword(s):  
Laminar Flow ◽  
Fine Particle ◽  
Pressure Effect ◽  
Diffusion Chamber ◽  
Particle Model

Dynamic Thin Laminar Flow Method for Making Protein Monolayers

Langmuir ◽  
1997 ◽  
Vol 13 (2) ◽  
pp. 264-276 ◽  
Author(s):  
G. Picard ◽  
I. Nevernov ◽  
D. Alliata ◽  
L. Pazdernik
Keyword(s):  
Laminar Flow ◽  
Flow Method ◽  
Protein Monolayers

scholarly journals Evaluation of fine particle formation by CVD in laminar-flow aerosol reactor.

1990 ◽  
Vol 16 (3) ◽  
pp. 526-534 ◽  
Author(s):  
Kikuo Okuyama ◽  
Ryuichi Ushio ◽  
Yasuo Kousaka ◽  
John H. Seinfeld ◽  
Richard C. Flagan
Keyword(s):  
Laminar Flow ◽  
Fine Particle ◽  
Particle Formation

Two-Dimensional Crystallization of Tetanus Toxin

1985 ◽  
Vol 43 ◽  
pp. 528-529
Author(s):  
Jeffry A. Reidler ◽  
John P. Robinson
Keyword(s):  
Electron Microscopy ◽  
Tetanus Toxin ◽  
Structural Information ◽  
Three Dimensional ◽  
Two Dimensional ◽  
Membrane Interface ◽  
3D Reconstructions ◽  
Cellular Receptors ◽  
Computer Reconstruction ◽  
2D Crystals

We have prepared two-dimensional (2D) crystals of tetanus toxin using procedures developed by Uzgiris and Kornberg for the directed production of 2D crystals of monoclonal antibodies at an antigen-phospholipid monolayer interface. The tetanus toxin crystals were formed using a small mole fraction of the natural receptor, GT1, incorporated into phosphatidyl choline monolayers. The crystals formed at low concentration overnight. Two dimensional crystals of this type are particularly useful for structure determination using electron microscopy and computer image refinement. Three dimensional (3D) structural information can be derived from these crystals by computer reconstruction of photographs of toxin crystals taken at different tilt angles. Such 3D reconstructions may help elucidate the mechanism of entry of the enzymatic subunit of toxins into cells, particularly since these crystals form directly on a membrane interface at similar concentrations of ganglioside GT1 to the natural cellular receptors.

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