scholarly journals Unified connected theory of few-body reaction mechanisms in N-body scattering theory

1978 ◽  
Author(s):  
W. N. Polyzou ◽  
E. F. Redish
1995 ◽  
Vol 18 (2-4) ◽  
pp. 213-227 ◽  
Author(s):  
Gy. Bencze ◽  
C. Chandler ◽  
A.G. Gibson ◽  
G.W. Pletsch

1997 ◽  
Vol 161 ◽  
pp. 611-621
Author(s):  
Guillermo A. Lemarchand ◽  
Fernando R. Colomb ◽  
E. Eduardo Hurrell ◽  
Juan Carlos Olalde

AbstractProject META II, a full sky survey for artificial narrow-band signals, has been conducted from one of the two 30-m radiotelescopes of the Instituto Argentino de Radioastronomía (IAR). The search was performed near the 1420 Mhz line of neutral hydrogen, using a 8.4 million channels Fourier spectrometer of 0.05 Hz resolution and 400 kHz instantaneous bandwidth. The observing frequency was corrected both for motions with respect to three astronomical inertial frames, and for the effect of Earths rotation, which provides a characteristic changing signature for narrow-band signals of extraterrestrial origin. Among the 2 × 1013spectral channels analyzed, 29 extra-statistical narrow-band events were found, exceeding the average threshold of 1.7 × 10−23Wm−2. The strongest signals that survive culling for terrestrial interference lie in or near the galactic plane. A description of the project META II observing scheme and results is made as well as the possible interpretation of the results using the Cordes-Lazio-Sagan model based in interstellar scattering theory.


Author(s):  
Jeff Gelles

Mechanoenzymes are enzymes which use a chemical reaction to power directed movement along biological polymer. Such enzymes include the cytoskeletal motors (e.g., myosins, dyneins, and kinesins) as well as nucleic acid polymerases and helicases. A single catalytic turnover of a mechanoenzyme moves the enzyme molecule along the polymer a distance on the order of 10−9 m We have developed light microscope and digital image processing methods to detect and measure nanometer-scale motions driven by single mechanoenzyme molecules. These techniques enable one to monitor the occurrence of single reaction steps and to measure the lifetimes of reaction intermediates in individual enzyme molecules. This information can be used to elucidate reaction mechanisms and determine microscopic rate constants. Such an approach circumvents difficulties encountered in the use of traditional transient-state kinetics techniques to examine mechanoenzyme reaction mechanisms.


Author(s):  
A. Angel ◽  
K. Miller ◽  
V. Seybold ◽  
R. Kriebel

Localization of specific substances at the ultrastructural level is dependent on the introduction of chemicals which will complex and impart an electron density at specific reaction sites. Peroxidase-antiperoxidase(PAP) methods have been successfully applied at the electron microscopic level. The PAP complex is localized by addition of its substrate, hydrogen peroxide and an electron donor, usually diaminobenzidine(DAB). On oxidation, DAB forms an insoluble polymer which is able to chelate with osmium tetroxide becoming electron dense. Since verification of reactivity is visual, discrimination of reaction product from osmiophillic structures may be difficult. Recently, x-ray microanalysis has been applied to examine cytochemical reaction precipitates, their distribution in tissues, and to study cytochemical reaction mechanisms. For example, immunoreactive sites labelled with gold have been ascertained by means of x-ray microanalysis.


Author(s):  
B. B. Chang ◽  
D. F. Parsons

The significance of dynamical scattering effects remains the major question in the structural analysis by electron diffraction of protein crystals preserved in the hydrated state. In the few cases (single layers of purple membrane and 400-600 Å thick catalase crystals examined at 100 kV acceleration voltage) where electron-diffraction patterns were used quantitatively, dynamical scattering effects were considered unimportant on the basis of a comparison with x-ray intensities. The kinematical treatment is usually justified by the thinness of the crystal. A theoretical investigation by Ho et al. using Cowley-Moodie multislice formulation of dynamical scattering theory and cytochrome b5as the test object2 suggests that kinematical analysis of electron diffraction data with 100-keV electrons would not likely be valid for specimen thickness of 300 Å or more. We have chosen to work with electron diffraction patterns obtained from actual wet protein crystals (rat hemoglobin crystals of thickness range 1000 to 2500 Å) at 200 and 1000 kV and to analyze these for dynamical effects.


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