5,617 research outputs found
LOWER BOUNDS FOR THE BUCKLING PRESSURE OF SPHERICAL SHELLS
Hydrostatic buckling pressure calculations for spherical shell
VSR symmetries in the DKP algebra: the interplay between Dirac and Elko spinor fields
VSR symmetries are here naturally incorporated in the DKP algebra on the
spin-0 and the spin-1 DKP sectors. We show that the Elko (dark) spinor fields
structure plays an essential role on accomplishing this aim, unravelling hidden
symmetries on the bosonic DKP fields under the action of discrete symmetries.Comment: 17 page
Flag-Dipole Spinor Fields in ESK Gravities
We consider the Riemann-Cartan geometry as a basis for the
Einstein-Sciama-Kibble theory coupled to spinor fields: we focus on and
conformal gravities, regarding the flag-dipole spinor fields, type-(4) spinor
fields under the Lounesto classification. We study such theories in specific
cases given for instance by cosmological scenarios: we find that in such
background the Dirac equation admits solutions that are not Dirac spinor
fields, but in fact the aforementioned flag-dipoles ones. These solutions are
important from a theoretical perspective, as they evince that spinor fields are
not necessarily determined by their dynamics, but also a discussion on their
structural (algebraic) properties must be carried off. Furthermore, the
phenomenological point of view is shown to be also relevant, since for
isotropic Universes they circumvent the question whether spinor fields do
undergo the Cosmological Principle.Comment: 18 pages, improved versio
Hsc66 substrate specificity is directed toward a discrete region of the iron-sulfur cluster template protein IscU
Hsc66 and Hsc20 comprise a specialized chaperone system important for the assembly of iron-sulfur clusters in Escherchia coli. Only a single substrate, the Fe/S template protein IscU, has been identified for the Hsc66/Hsc20 system, but the mechanism by which Hsc66 selectively binds IscU is unknown. We have investigated Hsc66 substrate specificity using phage display and a peptide array of IscU. Screening of a heptameric peptide phage display library revealed that Hsc66 prefers peptides with a centrally located Pro-Pro motif. Using a cellulose-bound peptide array of IscU we determined that Hsc66 interacts specifically with a region (residues 99-103, LPPVK) that is invariant among all IscU family members. A synthetic peptide (ELPPVKIHC) corresponding to IscU residues 98-106 behaves in a similar manner to native IscU, stimulating the ATPase activity of Hsc66 with similar affinity as IscU, preventing Hsc66 suppression of bovine rhodanese aggregation, and interacting with the peptide-binding domain of Hsc66. Unlike native IscU, however, the synthetic peptide is not bound by Hsc20 and does not synergistically stimulate Hsc66 ATPase activity with Hsc20. Our results indicate that Hsc66 and Hsc20 recognize distinct regions of IscU and further suggest that Hsc66 will not bind LPPVK motifs with high affinity in vivo unless they are in the context of native IscU and can be directed to Hsc66 by Hsc20
Unveiling Mapping Structures of Spinor Duals
Following the program of investigation of alternative spinor duals
potentially applicable to fermions beyond the standard model, we demonstrate
explicitly the existence of several well-defined spinor duals. Going further we
define a mapping structure among them and the conditions under which sets of
such dual maps do form a group. We also study the covariance of bilinear
quantities constructed with the several possible duals, the invariant
eigenspaces of those group elements and its connections with spinors
classification, as well as dual maps defined as elements of group algebras.Comment: 11 pages, no figure
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