The cyanobacterial ribosomal-associated protein LrtA from Synechocystis sp. PCC 6803 is an oligomeric protein in solution with chameleonic sequence properties

The LrtA protein of Synechocystis sp. PCC 6803 intervenes in cyanobacterial post-stress survival and in stabilizing 70S ribosomal particles. It belongs to the hibernating promoting factor (HPF) family of proteins, involved in protein synthesis. In this work, we studied the conformational preferences and stability of isolated LrtA in solution. At physiological conditions, as shown by hydrodynamic techniques, LrtA was involved in a self-association equilibrium. As indicated by Nuclear Magnetic Resonance (NMR), circular dichroism (CD) and fluorescence, the protein acquired a folded, native-like conformation between pH 6.0 and 9.0. However, that conformation was not very stable, as suggested by thermal and chemical denaturations followed by CD and fluorescence. Theoretical studies of its highly-charged sequence suggest that LrtA had a Janus sequence, with a context-dependent fold. Our modelling and molecular dynamics (MD) simulations indicate that the protein adopted the same fold observed in other members of the HPF family ( - - - - - ) at its N-terminal region (residues 1–100), whereas the C terminus (residues 100–197) appeared disordered and collapsed, supporting the overall percentage of overall secondary structure obtained by CD deconvolution. Then, LrtA has a chameleonic sequence and it is the first member of the HPF family involved in a self-association equilibrium, when isolated in solution.Ministerio de Economía y Competitividad CTQ2015-64445-RMinisterio de Economía y Competitividad BIO2016-78020-RMinisterio de Economía y Competitividad FIS2014-52212-RMinisterio de Economía y Competitividad BIO2016-75634-PFundación Séneca 19353/PI/1

. Microwave-assisted solvothermal controlled synthesis of Fe-Co

Syntheses of bimetallic cobalt-iron-based nanoparticles starting from Co(acac)2 and Fe(acac)3 (acac = acetylacetonate) were carried out by microwave-assisted solvothermal process, using ethylene glycol as the solvent and (polyvinylpyrrolidone) PVP, as the stabilizer. Indeed, the reaction mechanism in the presence of ethylene glycol is well understood [1] with the role of PVP being the inhibition of nanoparticles growth [2]. However, the control of the morphology of the synthetized nanoparticles is still a great challenge. Herein, we demonstrated that by adding amines to the reaction mixture, it is possible to control the morphology of the prepared bimetallic cobalt-iron materials. Thus, different Co-Fe micro-composites were synthetized by an innovative microwave assisted solvothermal synthesis, which allows to considerably reduce reaction time from 12 h to 15 min, with respect to classical thermal methods. The procedure was optimized by varying several parameters, such as: amount of PVP, in the presence or in the absence of amines, reaction temperature. The dark brown obtained powders were characterized by scanning electron microscopy, infrared spectroscopy and thermogravimetric analysis, confirming the beneficial effect of the presence of the amine in the morphology of the obtained composites. The obtained results open a new scenario for further studies on the possibility to control the morphology of bimetallic composite materials. [1] Fievet F, Lagier J P and Figlarz M Mater. Res. Soc. Bull. 24 (1989) 29–34 [2] Teranishi T, Kurita R and Miyake M J. Inorg. Organometall. Polym. 10 (2000) 145–5

Toward multitasking pharmacological COX-targeting agents: Non-steroidal anti-inflammatory prodrugs with antiproliferative effects

The antitumor activity of certain anti-inflammatory drugs is often attributed to an indirect effect based on the inhibition of COX enzymes. In the case of anti-inflammatory prodrugs, this property could be attributed to the parent molecules with mechanism other than COX inhibition, particularly through formulations capable of slowing down their metabolic conversion. In this work, a pilot docking study aimed at comparing the interaction of two prodrugs, nabumetone (NB) and its tricyclic analog 7-methoxy-2, 3-dihydro-1H-cyclopenta[b]naphthalen-1-one (MC), and their common active metabolite 6-methoxy-2-naphthylacetic acid (MNA) with the COX binding site, was carried out. Cytotoxicity, cytofluorimetry, and protein expression assays on prodrugs were also performed to assess their potential as antiproliferative agents that could help hypothesize an effective use as anticancer therapeutics. Encouraging results suggest that the studied compounds could act not only as precursors of the anti-inflammatory metabolite, but also as direct antiproliferative agents. © 2021 by the authors. Licensee MDPI, Basel, Switzerland

Polyacetylenes Bearing Chiral-Substituted Fluorene and Terfluorene Pendant Groups: Synthesis and Properties

The synthesis of the first polyacetylenes bearing chiral fluorene-based pendant groups is described. Poly{9,9-bis[(S)-3,7-dimethyloctyl]fluoren-2-ylacetylene} (PFA1), poly{9,9-bis[(S)-2-methylbutyl]- fluoren-2-ylacetylene} (PFA2), and poly{9,9,9′,9′,9′′,9′′-hexakis[(S)-2-methylbutyl]-7,2′;7′,2′′-terfluoren- 2-ylacetylene} (PFA3) have been obtained by Rh(I)-catalyzed polymerization of the corresponding terminal acetylene monomers 2-ethynyl-9,9-bis[(S)-3,7-dimethyloctyl]fluorene (2a), 2-ethynyl-9,9-bis[(S)-2-methylbutyl]fluorene (2b), and 2-ethynyl-9,9,9′,9′,9′′,9′′-hexakis[(S)-2-methylbutyl]-7,2′;7′,2′′-terfluorene (10). The effect of the alkyl chain length at the C-9 position of fluorene on the structural and conformational aspects of the polymers PFA1 and PFA2 as well as on their chiroptical properties was studied by XRD, DSC, TGA, GPC, UV-vis, and CD. A more planar conformation of the polyenic backbone of PFA1 with respect to PFA2 can be inferred by a red shift of the ð-ð* transition in the UV-vis spectra. Their photoluminescence properties are those typical of fluorene systems. CD measurements evidenced Cotton effects of opposite signs in correspondence of the backbone absorption region, ascribable to an excess of a screw sense of the helical conformations assumed by the two polymers. PFA3 revealed an amorphous structure and exhibited peculiar thermal stability features (as indicated by TGA and DSC). Its emission spectra interest the violet-blue region and do not show any substantial red shift passing from solution to solid state, thus pointing out an aggregation prevention of terfluorene groups by means of the polyacetylene backbone

Diagnosi di laboratorio e prevenzione delle emoglobinopatie: considerazioni e proposte sulla comunicazione del risultato degli esami di primo livello

Few documents concern the reporting of laboratory results in the field of hemoglobinopathies and thalassemic syndromes. Here we focus on how to report first level laboratory tests aimed to screen and detect hemoglobin variants and thalassemic defects. In doing this, motivation, pertinent information and possible conclusions are strictly connected

Microwave-assisted solvothermal synthesis of fe3o4/ceo2 nanocomposites and their catalytic activity in the imine formation from benzyl alcohol and aniline

Fe3O4/CeO2 nanocomposites were synthetized by coating magnetite seeds of different morphologies (hexagonal, spheroidal, quasi-spherical) with ceria, in ethylene glycol as solvothermal solvent. The synthesis was performed in the presence of microwave irradiation aiming to overcome the common disadvantages proper of the classic solvothermal/hydrothermal procedure. The obtained nanocomposites were calcined at the optimum temperature of 550 °C. The structure of the new nanomaterials was carefully investigated by IR, XRD, SEM, EDS and TEM analyses. The nanocomposites resulted to be constituted by CeO2 nanoparticles distributed onto Fe3O4 seeds, that kept their pristine morphology. The new materials were used as catalysts for imine synthesis from benzyl alcohol and aniline. The highest imine conversion rate was obtained with Fe3O4/CeO2, which was synthesized from Fe3O4 nanoparticles (hexagonal) obtained by microwave hydrothermal procedure in the absence of any organic additive (polyvinylpyrrolidone, trisodium citrate dihydrate or oleic acid). The catalyst could be easily removed from the reaction mixture with the help of an external magnet, and it was recycled for at least five runs with increasing catalytic activit

Microwave-assisted solvothermal synthesis of fe3o4/ceo2 nanocomposites and their catalytic activity in the imine formation from benzyl alcohol and aniline

Fe3O4/CeO2 nanocomposites were synthetized by coating magnetite seeds of different morphologies (hexagonal, spheroidal, quasi-spherical) with ceria, in ethylene glycol as solvothermal solvent. The synthesis was performed in the presence of microwave irradiation aiming to overcome the common disadvantages proper of the classic solvothermal/hydrothermal procedure. The obtained nanocomposites were calcined at the optimum temperature of 550 °C. The structure of the new nanomaterials was carefully investigated by IR, XRD, SEM, EDS and TEM analyses. The nanocomposites resulted to be constituted by CeO2 nanoparticles distributed onto Fe3O4 seeds, that kept their pristine morphology. The new materials were used as catalysts for imine synthesis from benzyl alcohol and aniline. The highest imine conversion rate was obtained with Fe3O4/CeO2, which was synthesized from Fe3O4 nanoparticles (hexagonal) obtained by microwave hydrothermal procedure in the absence of any organic additive (polyvinylpyrrolidone, trisodium citrate dihydrate or oleic acid). The catalyst could be easily removed from the reaction mixture with the help of an external magnet, and it was recycled for at least five runs with increasing catalytic activity