scholarly journals Reduction of spectroscopic strength: Weakly-bound and strongly-bound single-particle states studied using one-nucleon knockout reactions

2008 ◽  
Vol 77 (4) ◽  
Author(s):  
A. Gade ◽  
P. Adrich ◽  
D. Bazin ◽  
M. D. Bowen ◽  
B. A. Brown ◽  
...  
2001 ◽  
Vol 682 (1-4) ◽  
pp. 332-338 ◽  
Author(s):  
V. Maddalena ◽  
T. Aumann ◽  
D. Bazin ◽  
B.A. Brown ◽  
J.A. Caggiano ◽  
...  

2008 ◽  
Vol 23 (27n30) ◽  
pp. 2589-2592 ◽  
Author(s):  
G. SAXENA ◽  
D. SINGH ◽  
H. L. YADAV ◽  
A. HAGA ◽  
H. TOKI

Inspired by recent measurements indicating proton magic number at Z =14 in the vicinity of 42 Si , we have employed our relativistic mean-field (RMF) plus state dependent BCS approach for the study of even-even nuclei to obtain magic numbers and to look for nuclei exhibiting weakly bound structures and even halo formation. In our RMF+BCS approach the single particle continuum corresponding to the RMF is replaced by a set of discrete positive energy states for the calculations of pairing energy. It is found that in several nuclei the filling in of low lying single particle resonant state with large angular momentum, even before it becomes a bound state, helps to accommodate more neutrons but with extremely small increase in the binding energy. This gives rise to the occurrence of weakly bound system of neutron rich nuclei.


1999 ◽  
Author(s):  
A. Navin ◽  
T. Aumann ◽  
D. Bazin ◽  
B. A. Brown ◽  
T. Glasmacher ◽  
...  

2014 ◽  
Vol 92 (3) ◽  
pp. 253-258 ◽  
Author(s):  
G. Saxena ◽  
D. Singh ◽  
M. Kaushik ◽  
S. Somorendro Singh

We have employed the relativistic mean field (RMF)+BCS approach, to study ground state properties of drip line isotopes of Si. In this approach the single particle continuum corresponding to the RMF is replaced by a set of discrete positive energy states for the calculations of pairing energy. Detailed analysis of separation energy, single particle spectrum, pairing energies, and densities of the nuclei predict weakly bound structure in neutron-rich Si isotopes, which is seen to be due to the large spatial extension of the wave functions for the weakly bound single particle states with low orbital angular momentum having very small centrifugal barriers.


Author(s):  
J. Frank ◽  
P.-Y. Sizaret ◽  
A. Verschoor ◽  
J. Lamy

The accuracy with which the attachment site of immunolabels bound to macromolecules may be localized in electron microscopic images can be considerably improved by using single particle averaging. The example studied in this work showed that the accuracy may be better than the resolution limit imposed by negative staining (∽2nm).The structure used for this demonstration was a halfmolecule of Limulus polyphemus (LP) hemocyanin, consisting of 24 subunits grouped into four hexamers. The top view of this structure was previously studied by image averaging and correspondence analysis. It was found to vary according to the flip or flop position of the molecule, and to the stain imbalance between diagonally opposed hexamers (“rocking effect”). These findings have recently been incorporated into a model of the full 8 × 6 molecule.LP hemocyanin contains eight different polypeptides, and antibodies specific for one, LP II, were used. Uranyl acetate was used as stain. A total of 58 molecule images (29 unlabelled, 29 labelled with antl-LPII Fab) showing the top view were digitized in the microdensitometer with a sampling distance of 50μ corresponding to 6.25nm.


Author(s):  
Adriana Verschoor ◽  
Ronald Milligan ◽  
Suman Srivastava ◽  
Joachim Frank

We have studied the eukaryotic ribosome from two vertebrate species (rabbit reticulocyte and chick embryo ribosomes) in several different electron microscopic preparations (Fig. 1a-d), and we have applied image processing methods to two of the types of images. Reticulocyte ribosomes were examined in both negative stain (0.5% uranyl acetate, in a double-carbon preparation) and frozen hydrated preparation as single-particle specimens. In addition, chick embryo ribosomes in tetrameric and crystalline assemblies in frozen hydrated preparation have been examined. 2D averaging, multivariate statistical analysis, and classification methods have been applied to the negatively stained single-particle micrographs and the frozen hydrated tetramer micrographs to obtain statistically well defined projection images of the ribosome (Fig. 2a,c). 3D reconstruction methods, the random conical reconstruction scheme and weighted back projection, were applied to the negative-stain data, and several closely related reconstructions were obtained. The principal 3D reconstruction (Fig. 2b), which has a resolution of 3.7 nm according to the differential phase residual criterion, can be compared to the images of individual ribosomes in a 2D tetramer average (Fig. 2c) at a similar resolution, and a good agreement of the general morphology and of many of the characteristic features is seen.Both data sets show the ribosome in roughly the same ’view’ or orientation, with respect to the adsorptive surface in the electron microscopic preparation, as judged by the agreement in both the projected form and the distribution of characteristic density features. The negative-stain reconstruction reveals details of the ribosome morphology; the 2D frozen-hydrated average provides projection information on the native mass-density distribution within the structure. The 40S subunit appears to have an elongate core of higher density, while the 60S subunit shows a more complex pattern of dense features, comprising a rather globular core, locally extending close to the particle surface.


Author(s):  
John Trinickt ◽  
Howard White

The primary force of muscle contraction is thought to involve a change in the myosin head whilst attached to actin, the energy coming from ATP hydrolysis. This change in attached state could either be a conformational change in the head or an alteration in the binding angle made with actin. A considerable amount is known about one bound state, the so-called strongly attached state, which occurs in the presence of ADP or in the absence of nucleotide. In this state, which probably corresponds to the last attached state of the force-producing cycle, the angle between the long axis myosin head and the actin filament is roughly 45°. Details of other attached states before and during power production have been difficult to obtain because, even at very high protein concentration, the complex is almost completely dissociated by ATP. Electron micrographs of the complex in the presence of ATP have therefore been obtained only after chemically cross-linking myosin subfragment-1 (S1) to actin filaments to prevent dissociation. But it is unclear then whether the variability in attachment angle observed is due merely to the cross-link acting as a hinge.We have recently found low ionic-strength conditions under which, without resorting to cross-linking, a high fraction of S1 is bound to actin during steady state ATP hydrolysis. The structure of this complex is being studied by cryo-electron microscopy of hydrated specimens. Most advantages of frozen specimens over ambient temperature methods such as negative staining have already been documented. These include improved preservation and fixation rates and the ability to observe protein directly rather than a surrounding stain envelope. In the present experiments, hydrated specimens have the additional benefit that it is feasible to use protein concentrations roughly two orders of magnitude higher than in conventional specimens, thereby reducing dissociation of weakly bound complexes.


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