High-resolution 2-DE for resolving proteins, protein adducts and complexes in plasma

A 2-DE system has been devised in which proteins are first separated in their native state followed by separation according to mass under denaturing conditions (Nat/SDS-PAGE). Hydrophilic properties of the gel and the presence of dihydroxybisacrylamide in the first dimension allowed a good resolution for high-molecular-weight proteins and maintained interactions. With this method 252 plasma spots have been resolved and 140 have been characterized by MS as isoforms of 60 proteins, a relevant part of which (12) were not detected by traditional 2-D gels or by other nondenaturing 2-D techniques. The list includes complement factors (C4d, C7), coagulation factors (coagulation factor II, fibrin beta), apolipoproteins (apolipoprotein B) and cell debris (vinculin, gelsolin, tropomyosin, dystrobrevin beta, fibrinectin I). Nat/SDS PAGE also allowed separation of nicked forms of albumin, Apo B100 and alpha2-macroglobulin and showed the presence of atypical albumin adducts corresponding to post-translational and oxidation products. Our system provides therefore new tools for resolving proteins, protein aggregates and complexes and amplifies the potentiality of traditional electrophoretic analysis.     

Gels dried under supercritical and ambient conditions: a comparative study and their subsequent conversion to silica–carbon composite aerogels

In present work, we have prepared gels with various compositions of methyltrimethoxysilane—3-(2,3-epoxypropoxy) propyltrimethoxysilane (MTMS-GPTMS) using a two-step acid base sol–gel process. To make a comparative study between the two common drying routes, we prepared gels under supercritical and also under ambient conditions. The density of the supercritically dried hybrid aerogels lies between 0.18 and 0.31 gcm^?3, while the density of the ambient dried ones ranges between 0.35 and 0.42 gcm^?3. The surface area of MTMS-0.25 GPTMS aerogel dried under supercritical conditions, has been found to be 464 m² g^?1 with a pore volume and average pore diameter of 1.24 cm³ g^?1 and 11 nm respectively. The same composition dried under ambient conditions is found to have similar properties i.e. a BET surface area of 439 m² g^?1, pore volume of 1.22 cm³ g^?1 and average pore diameter of 11 nm. The aerogels were later pyrolyzed yielding silica/carbon composite aerogels. The pyrolized aerogels possessed a surface area as high as 207 m² g^?1 with a total pore volume of 0.98 cm³ g^?1. The pyrolysed aerogels were also calcined to yield carbon free materials.     

Amphiphilic antioxidants from "cashew nut shell liquid" (CNSL) waste

Hydrogenated cardanol and cardols, contained in industrial grade cardanol oil and obtained by distillation of the raw "cashew nut shell liquid" (CNSL), are easily transformed into efficient 4-thiaflavane antioxidants bearing a long alkyl chain on A ring and a catechol group on B ring.     

Reversible interconversion between a supramolecular polymer and a discrete octameric species from a guanosine derivative by dynamic cation binding and release

[reaction: see text] The tunable interconversion between two highly ordered supramolecular motifs (G-quartet K(+)-templated column and G-ribbon) of a lipophilic guanosine derivative fueled by cation complexation and release in a cryptand [2.2.2] containing guanosine solution is reported. The process is controlled by the sequential addition of acid and base.     

Inclusive ∑±(1385) production inK − p interactions at 110 GeV/c

Results are presented on inclusive production of ∑⁺(1385) and ∑^?(1385) inK ^? p interactions at 110 GeV/c. The inclusive and topological cross sections have been estimated and compared with published results at lower energies. The inclusive cross section of ∑⁺(1385) seems to decrease with c.m. energy, while that of the ∑^?(1385) is nearly constant. The mean charged multiplicity associate to Σ(1385) increases with c.m. energy. The ∑⁺(1385) is produced both in the target fragmentation region and in the central region where ∑^?(1385) is predominantly produced in the central region. Approximately 16% of the Λ's stem from the decay of ∑^±(1385) and the kinematic distributions of these Λ's are not very different from the inclusive Λ's.     

Probing High-Scale and Split Supersymmetry with Higgs mass measurements

We study the range of Higgs masses predicted by High-Scale Supersymmetry and by Split Supersymmetry, using the matching condition for the Higgs quartic coupling determined by the minimal field content. In the case of Split Supersymmetry, we compute for the first time the complete next-to-leading order corrections, including two-loop renormalization group equations and one loop threshold effects. These corrections reduce the predicted Higgs mass by a few GeV. We investigate the impact of the recent LHC Higgs searches on the scale of supersymmetry breaking. In particular, we show that an upper bound of 127 GeV on the Higgs mass implies an upper bound on the scale of Split Supersymmetry of about ¹⁰⁸ GeV, while no firm conclusion can yet be drawn for High-Scale Supersymmetry.     

Selective adsorption in elastic and inelastic scattering of He and Ne from LiF (001) surface

New experimental evidence is presented for selective adsorption in the inelastic, as well the elastic scattering of He and Ne from LiF. For the inelastic scattering a condition for the effect is derived, by which it is possible to obtain, merely from the position of minima in the inelastic spectrum, an averaged excitation spectrum. The results thus found are entirely consistent with the present knowledge of the surface dynamics of LiF.     

Neutron diffraction study of UAs in high magnetic fields

Magnetization experiments have shown that at low temperature and in an applied magnetic field of ～90 kOe antiferromagnetic (AF) uranium arsenide transforms to a new ferrimagnetic state. The high-field transition produces a state with magnetic components $\text{parallel}$ to the applied field. A small ferromagnetic component (0.4 μ_B) is seen in magnetization experiments but with neutron diffraction we have observed directly the large AF component (～ 1.8 μ_B) which has a $\text{q}$ value of 0.58 ± 0.01 $\text{c}$¹ in contrast to the zero field type IA structure with $\text{q}\text{= (0,0,0.50)}$. This transition is quite different from that occuring in the conventional spin-flop transition.     

On the Conformation of a Sterically Congested Amide Group in the Crystalline State and in Solution

The conformation in the crystalline state and in solution of the sterically congested tetramethylpiperidinederived amide group of the symmetric diamide I formed from 2,2,6,6-tetramethylpiperidine ( b ) and 1,2,5-thiadiazole-3,4-dicarbonyl dichloride ( c ), and of the mixed diamide II derived from b , c , and piperidine ( a ) has been investigated. In crystals, as observed with II , this group is strongly bent out-of-plane at both the N-atom and the carbonyl C-atom, and there is also a sizable twisting around the amide bond. Furthermore, the amide bond is abnormally long (1.37 Å). In CD₂Cl₂ (or CDCl₃) solution, the group is apparently planar in its ground-state conformation, but the energy barrier to rotation around the amide bond is low. This conclusion is based on low-temperature ¹H-NMR measurements on I , II , and on the symmetric diamide III derived from a and c .