Smoothability and order bound for AS semigroups

In this paper we consider numerical semigroups S generated by arithmetic sequences m ₀,??,m _n (AS-semigroups). First we state some results on the module $T^{1}_{k[S]}$ ; further in the cases m ₀??1 and m ₀??n (modulo n), we prove these semigroups are Weierstrass by showing that the associated monomial curves $X=\operatorname {Spec}{k[S]}$ are smoothable. Finally for each semigroup S generated by an arithmetic sequence we evaluate the so-called ??order bounds??: when S is Weierstrass, these invariants are good approximations for the minimum distance of the related one-point codes.     

Using high pressure to prepare polymorphs of the Ba2Co(1-x)Zn(x)S3 (0 ≤ x ≤ 1.0) compounds

In this work, high pressure was used as a tool to induce structural transition and prepare metastable polymorphs of ternary sulfides. Structural transformations under high pressure of compounds belonging to the Ba(2)Co(1-x)Zn(x)S(3) (0 ≤ x ≤ 1.0) series were studied using X-ray diffraction and electron microscopy. All members of the Ba(2)Co(1-x)Zn(x)S(3) series show the Ba(2)CoS(3)-type one-dimensional structure, but, after heating under pressure, the Ba(2)CoS(3) compound (x = 0) separates into BaS and the two-dimensional BaCoS(2-δ) (δ ≈ 0), while Ba(2)Co(1-x)Zn(x)S(3) compounds with x ≥ 0.25 maintain their one-dimensional features but rearrange into polymorphs showing the Ba(2)MnS(3)-type structure. All structural transformations can be linked to shortening in interchain metal-metal distances caused by the high pressure, and the role of the zinc in preventing loss of one-dimensionality is discussed.     

Toward a stable α-cycloalkyl amino acid with a photoswitchable cationic side chain

The N-alkylated indanylidenepyrroline (NAIP) Schiff base 3 is an unnatural α-amino acid precursor potentially useful for the preparation of semisynthetic peptides and proteins incorporating charged side chains whose structure can be modulated via Z/E photoisomerization. Here we report that the heteroallylic protons of 3 led to partial loss of ethanol accompanied by formation of the novel heterocyclic system 4 during attempted deprotection. We also show that the same protons catalyze the thermal isomerization of 3, making the light-driven conformational control concept ineffective for times longer than a few hours. These problems are not present in the previously unreported compound 5 where the acidic methyl group is replaced by an H atom. Therefore, 5, rather than 3, constitutes a promising prototype for the design of building blocks capable to modulate the electrostatic potential of a protein in specific locations via light irradiation.     

Numerical methods for Fredholm integral equations on the square

In this paper we shall investigate the numerical solution of two-dimensional Fredholm integral equations by Nyström and collocation methods based on the zeros of Jacobi orthogonal polynomials. The convergence, stability and well conditioning of the method are proved in suitable weighted spaces of functions. Some numerical examples illustrate the efficiency of the methods.     

Proteomic characterization of donkey milk “caseome”

At present, compared with bovine milk, the characterization of donkey milk caseins is at a relatively early stage progress, and only limited data are related to its genetic polymorphism. In this work, the heterogeneity of donkey caseome was investigated using a proteomic approach, based on one- (PAGE, UTLIEF) and two-dimensional (PAGE → UTLIEF) electrophoresis, stained with either Coomassie Brilliant Blue or specific polyclonal antibodies, and structural MS analysis. These combined methodologies allowed the contemporary identification of donkey α_s1, α_s2, β and κ-CN with their related heterogeneity due to phosphorylation (α_s1, α_s2 and β-CN), glycosylation (κ-CN) and incorrect splicing of RNA in mRNA (deleted forms of α_s1-CN and β-CN). The results achieved showed 11 components for κ-CN, six phosphorylated components for β and α_s1-CN and three main phosphorylated components for α_s2-CN, each accounting for 10, 11 and 12 P/mole. At this regard, for the first time, the primary structure of the expressed protein corresponding to the only available donkey α_s2-CN cDNA sequence was determined. Furthermore β-CN was found in homozygous and heterozygous state for the occurrence of a genetic β-CN variant having a MW value 28 mass units higher than the common β-CN phenotype.     

Temperature‐induced self‐assembly of degalactosylated xyloglucan at low concentration

Xyloglucan is a natural polysaccharide having a cellulose‐like backbone and hydroxyl groups‐rich side‐chains. In its native form the polymer is water‐soluble and forms gel only in presence of selected co‐solutes. When a given fraction of galactosyl residues are removed by enzymatic reaction, the polymer acquires the ability to form a gel in aqueous solution at physiological temperatures, a property of great interest for biomedical/pharmaceutical applications. This work presents data on the effect of a temperature increase on degalactosylated xyloglucan dispersed in water at concentration low enough not to run into macroscopic gelation. Results obtained over a wide interval of length scales show that, on increasing temperature, individual polymer chains and pre‐existing clusters self‐assemble into larger structures. The process implies a structural rearrangement over a few nanometers scale and an increase of dynamics homogeneity. The relation of these findings to coil‐globule transition and phase separation is discussed. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 1727–1735     

Templateless synthesis of polypyrrole nanowires by non-static solution-surface electropolymerization

Polypyrrole nanowires (PPy-NWs) are synthesized by a novel templateless approach based on non-static solution-surface (NSSS) electropolymerization. The mechanism responsible for PPy-NW formation is the simultaneous oxidation of pyrrole and water, with concomitant formation of hydroxyl radicals and dioxygen nanobubbles. In particular, a localized PPy-NW deposition at the solution-air interface is enabled by solution-surface electropolymerization due to the surface excess of the monomer at the interface favored by the large surface tension of the solvent. In the proposed approach, solution-surface electropolymerization is performed in non-static conditions (NSSS), as the solution-air interface is shifted by flowing the electrolyte solution over the electrode surface. This allows a PPy-NW homogeneous deposition on whatever large area electrode to be rapidly achieved. Parameters influencing the morphology of PPy-NWs are studied, particularly focusing on flow rate, pH of the electrolyte solution, and electropolymerization time. The growth process of PPy-NWs is examined and the way of tuning their resulting morphology is discussed. Morphological investigation by scanning electron microscopy and chemical/electrochemical characterization of PPy-NWs by X-ray photoelectron spectroscopy and cyclic voltammetry, respectively, further support the proposed nanowire formation mechanism. Nanowires with diameter in the range of 40–300 nm are obtained, and the possibility of depositing differently sized nanowires with a predetermined spatial distribution on the same substrate is also demonstrated.     

Copper(I) and copper(II) inhibit Aβ peptides proteolysis by insulin-degrading enzyme differently: implications for metallostasis alteration in Alzheimer's disease

Accumulation of neurotoxic amyloid-β peptide (Aβ) and alteration of metal homeostasis (metallostasis) in the brain are two main factors that have been very often associated with neurodegenerative diseases, such as Alzheimer's disease (AD). Aβ is constantly produced from the amyloidprecursor-protein APP precursor and immediately catabolized under normal conditions, whereas dysmetabolism of Aβ and/or metal ions seems to lead to a pathological deposition. Although insulin-degrading enzyme (IDE) is the main metalloprotease involved in Aβ degradation in the brain being up-regulated in some areas of AD brains, the role of IDE for the onset and development of AD is far from being understood. Moreover, the biomolecular mechanisms involved in the recognition and interaction between IDE and its substrates are still obscure. In spite of the important role of metals (such as copper, aluminum, and zinc), which has brought us to propose a "metal hypothesis of AD", a targeted study of the effect of metallostasis on IDE activity has never been carried out. In this work, we have investigated the role that various metal ions (i.e., Cu(2+), Cu(+), Zn(2+), Ag(+), and Al(3+)) play in modulating the interaction between IDE and two Aβ peptide fragments, namely Aβ(1-16) and Aβ(16-28). It was therefore possible to identify the direct effect that such metal ions have on IDE structure and enzymatic activity without interferences caused by metal-induced substrate modifications. Mass spectrometry and kinetic studies revealed that, among all the metal ions tested, only Cu(2+), Cu(+), and Ag(+) have an inhibitory effect on IDE activity. Moreover, the inhibition of copper(II) is reversed by adding zinc(II), whereas the monovalent cations affect the enzyme activity irreversibly. The molecular basis of their action on the enzyme is also discussed on the basis of computational investigations.