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[Hypothesis]: Graphene oxide-based nanotechnology has aroused a great interest due to its applications in the biomedical and optoelectronic fields. The wide use of these materials makes it necessary to study its potential toxicity associated with the inhalation of Graphene Oxide (GO) nanoparticles and its interaction with the lung surfactant. Langmuir monolayers have proven to be an excellent tool for studying the properties of the lung surfactant and the effect of intercalation of nanoparticles on its structure and properties. Therefore, to know the origin of the phospholipids/GO interaction and the structure of the lipid layer with GO, in this work we study the effect of the insertion of GO sheets on a Langmuir film of 1,2-Dipalmitoyl-sn-glycerol-3-phosphocholine (DPPC)., [Experiments]: Surface pressure-area isotherms, Neutron (NR) and X-ray Reflectivity (XRR) and Grazing Incidence X-ray Diffraction (GIXD) measurements of hydrogenated and deuterated DPPC monolayers with and without GO have been carried out., [Findings]: The results outline a strong interaction between the GO and the zwitterionic form of DPPC and prove that GO is in three regions of the DPPC monolayer, the aliphatic chains of DPPC, the head groups and water in the subphase. Comparison between results obtained with hydrogenated and deuterated DPPC allows concluding that both, electrostatic attractions, and dispersion forces are responsible of the interaction GO/DPPC. Results also demonstrated that the insertion of GO into the DPPC aliphatic chains does not induce significant changes on unit cell of DPPC.

The bacterial cell-wall peptidoglycan is made of glycan strands crosslinked by short peptide stems. Crosslinks are catalyzed by DD-transpeptidases (4,3-crosslinks) and LD-transpeptidases (3,3-crosslinks). However, recent research on non-model species has revealed novel crosslink types, suggesting the existence of uncharacterized enzymes. Here, we identify an LD-transpeptidase, LDTGo, that generates 1,3-crosslinks in the acetic-acid bacterium Gluconobacter oxydans. LDTGo-like proteins are found in Alpha- and Betaproteobacteria lacking LD3,3-transpeptidases. In contrast with the strict specificity of typical LD- and DD-transpeptidases, LDTGo can use non-terminal amino acid moieties for crosslinking. A high-resolution crystal structure of LDTGo reveals unique features when compared to LD3,3-transpeptidases, including a proline-rich region that appears to limit substrate access, and a cavity accommodating both glycan chain and peptide stem from donor muropeptides. Finally, we show that DD-crosslink turnover is involved in supplying the necessary substrate for LD1,3-transpeptidation. This phenomenon underscores the interplay between distinct crosslinking mechanisms in maintaining cell wall integrity in G. oxydans.

We explore a simple and optimized approach for obtaining magnetic nanoparticle-carbon composites by a novel one-pot sol-gel method. In them, various metal cations ratios of Fe3+ and Co2+ are evaluated. The ratio of Fe:Co is a critical parameter that governs the presence of different crystalline phases with tailored magnetic properties. Interestingly, the smallest introduction of Co into the synthesis (19Fe:1Co) provides an abrupt emergence of the body-centered cubic (bcc) Fe-Co alloy, instead of the orthorhombic Pnma structure characteristic of the Fe3C intermetallic compound (1Fe:0Co). Advanced structural and electronic characterizations reveal the formation of Fe-Co/Co-ferrite core/shell nanoparticle structures embedded in a carbon matrix. The sphere-like nanoparticles range from 10 to 45 nm and the shells show a spinel structure with a thickness of 2–3 nm. In addition, X-ray absorption spectroscopy unveils that the oxidation state of Fe and Co cations is close to zero, demonstrating their predominant metallic character. The magnetic properties can be modulated by a precise control of the alloy composition varying the Co content, displaying saturation magnetization values close to ∼137 emu/g. The nanoparticles are mainly single magnetic domain with a considerable coercive field (∼450 Oe), higher than those reported in the literature for Fe-Co nanoparticles. This semi-hard character is due to a notable spring exchange effect emerged by passivating the surface of Fe-Co-bcc cores with a thin Co-ferrite-like shell.

Taxanes are microtubule-stabilizing agents used in the treatment of many solid tumors, but they often involve side effects affecting the peripheral nervous system. It has been proposed that this could be related to structural modifications on the filament upon drug binding. Alternatively, laulimalide and peloruside bind to a different site also inducing stabilization, but they have not been exploited in clinics. Here, we use a combination of the parental natural compounds and derived analogs to unravel the stabilization mechanism through this site. These drugs settle lateral interactions without engaging the M loop, which is part of the key and lock involved in the inter-protofilament contacts. Importantly, these drugs can modulate the angle between protofilaments, producing microtubules of different diameters. Among the compounds studied, we have found some showing low cytotoxicity and able to induce stabilization without compromising microtubule native structure. This opens the window of new applications for microtubule-stabilizing agents beyond cancer treatment.

The mechanism of hydration of calcium sulfate hemihydrate (CaSO·0.5HO) to form gypsum (CaSO·2HO) was studied by combining scanning 3D X-ray diffraction (s3DXRD) and phase contrast tomography (PCT) to determine in situ the spatial and crystallographic relationship between these two phases. From s3DXRD measurements, the crystallographic structure, orientation and position of the crystalline grains in the sample during the hydration reaction were obtained, while the PCT reconstructions allowed visualization of the 3D shapes of the crystals during the reaction. This multi-scale study unfolds structural and morphological evidence of the dissolution–precipitation process of the gypsum plaster system, providing insights into the reactivity of specific crystallographic facets of the hemihydrate. In this work, epitaxial growth of gypsum crystals on the hemihydrate grains was not observed.

Van der Waals (vdW) heterostructures combining layered ferromagnets and other 2D crystals are promising building blocks for the realization of ultracompact devices with integrated magnetic, electronic, and optical functionalities. Their implementation in various technologies depends strongly on the development of a bottom-up scalable synthesis approach allowing for realizing highly uniform heterostructures with well-defined interfaces between different 2D-layered materials. It is also required that each material component of the heterostructure remains functional, which ideally includes ferromagnetic order above room temperature for 2D ferromagnets. Here, it is demonstrated that the large-area growth of Fe5−xGeTe2/graphene heterostructures is achieved by vdW epitaxy of Fe5−xGeTe2 on epitaxial graphene. Structural characterization confirms the realization of a continuous vdW heterostructure film with a sharp interface between Fe5−xGeTe2 and graphene. Magnetic and transport studies reveal that the ferromagnetic order persists well above 300 K with a perpendicular magnetic anisotropy. In addition, epitaxial graphene on SiC(0001) continues to exhibit a high electronic quality. These results represent an important advance beyond nonscalable flake exfoliation and stacking methods, thus marking a crucial step toward the implementation of ferromagnetic 2D materials in practical applications.

Acetylcholine is a central biological signal molecule present in all kingdoms of life. In humans, acetylcholine is the primary neurotransmitter of the peripheral nervous system; it mediates signal transmission at neuromuscular junctions. Here, we show that the opportunistic human pathogen Pseudomonas aeruginosa exhibits chemoattraction toward acetylcholine over a concentration range of 1 mM to 100 mM. The maximal magnitude of the response was superior to that of many other P. aeruginosa chemoeffectors. We demonstrate that this chemoattraction is mediated by the PctD (PA4633) chemoreceptor. Using microcalorimetry, we show that the PctD ligand-binding domain (LBD) binds acetylcholine with a equilibrium dissociation constant (KD) of 23 mM. It also binds choline and with lower affinity betaine. Highly sensitive responses to acetylcholine and choline, and less sensitive responses to betaine and L-carnitine, were observed in Escherichia coli expressing a chimeric receptor comprising the PctD-LBD fused to the Tar chemoreceptor signaling domain. We also identified the PacA (ECA_RS10935) chemoreceptor of the phytopathogen Pectobacterium atrosepticum, which binds choline and betaine but fails to recognize acetylcholine. To identify the molecular determinants for acetylcholine recognition, we report high-resolution structures of PctD-LBD (with bound acetylcholine and choline) and PacA-LBD (with bound betaine). We identified an amino acid motif in PctD-LBD that interacts with the acetylcholine tail. This motif is absent in PacA-LBD. Significant acetylcholine chemotaxis was also detected in the plant pathogens Agrobacterium tumefaciens and Dickeya solani. To the best of our knowledge, this is the first report of acetylcholine chemotaxis and extends the range of host signals perceived by bacterial chemoreceptors.

MgO ultrathin films are of great technological importance as electron tunneling barrier in electronics and spintronics, and as template for metallic clusters in catalysis and for molecular networks for 2D electronics. The wide band-gap of MgO allows for a very effective decoupling from the substrate. The films morphology and the detailed structure of the interface are crucial for applications, controlling the electronic transfer. Using surface x-ray diffraction, we studied the growth-mode and the structure of MgO/Ag(001) ultrathin films elaborated by reactive molecular beam epitaxy as function of the substrate temperature. We observed that deposition of about 1 monolayer results in an MgO(001) film in coherent epitaxy, with the oxygen atoms on top of silver as predicted by DFT calculations, and an interlayer distance at the interface of about 270 pm. Under well-defined conditions, a sharp MgO bilayer is formed covering a fraction of the substrate surface.

Nanowire chip-based electrical and optical devices such as biochemical sensors, physical detectors, or light emitters combine outstanding functionality with a small footprint, reducing expensive material and energy consumption. The core functionality of many nanowire-based devices is embedded in their p-n junctions. To fully unleash their potential, such nanowire-based devices require – besides a high performance – stability and reliability. Here, we report on an axial p-n junction GaAs nanowire X-ray detector that enables ultra-high spatial resolution (~200 nm) compared to micron scale conventional ones. In-operando X-ray analytical techniques based on a focused synchrotron X-ray nanobeam allow probing the internal electrical field and observing hot electron effects at the nanoscale. Finally, we study device stability and find a selective hot electron induced oxidization in the n-doped segment of the p-n junction. Our findings demonstrate capabilities and limitations of p-n junction nanowires, providing insight for further improvement and eventual integration into on-chip devices.

In this paper, montmorillonite functionalized with a Cu(II)-phenanthroline complex (Mt-CuPhen) and then exposed to heptanethiol vapors (Mt-CuPhen-HPT) was tested for the capture of halobenzenes in gas phase. The treatment of Mt-CuPhen with heptanethiol vapors produced important compositional changes involving Cu(II) reduction, oxidation of thiol to disulfide and dehydration of the mineral interlayer space. Entrapping experiments were carried out on fluorobenzene, chlorobenzene and bromobenzene at 25 and 45 °C. The hybrid material proved to be very efficient for all halobenzenes and especially for fluorobenzene. Observed performances are slightly affected by temperature. Halobenzene desorption occurred even at 100 °C, a temperature quite lower than that required for decomposition of Mt-CuPhen-HPT. The Mt-CuPhen-HPT hybrid material, therefore, can be reused several times and requires low energy costs for regeneration. An alternative regeneration procedure based on disulfide removal has been proposed as well. Mt-CuPhen-HPT was extensively characterized before and after halobenzenes immobilization through elemental analysis, UV–Vis measurements, thermogravimetric analyses, FTIR, NMR and X-ray absorption spectroscopies.

Enzyme engineering has allowed not only the de novo creation of active sites catalysing known biological reactions with rates close to diffusion limits, but also the generation of abiological sites performing new-to-nature reactions. However, the catalytic advantages of engineering multiple active sites into a single protein scaffold are yet to be established. Here, we report on proteins with two active sites of biological and/or abiological origin, for improved natural and non-natural catalysis. The approach increased the catalytic properties, such as enzyme efficiency, substrate scope, stereoselectivity and optimal temperature window, of an esterase containing two biological sites. Then, one of the active sites was metamorphosed into a metal-complex chemocatalytic site for oxidation and Friedel–Crafts alkylation reactions, facilitating synergistic chemo- and biocatalysis in a single protein. The transformations of 1-naphthyl acetate into 1,4-naphthoquinone (conversion approx. 100%) and vinyl crotonate and benzene into 3-phenylbutyric acid (≥83%; e.e. >99.9%) were achieved in one pot with this artificial multifunctional metalloenzyme.

[EN] Keggin [PW12O40]3– and Wells–Dawson [P2W18O62]6– heteropolyanions are nanosized transition-metal-oxygen clusters belonging to the heteropolyacids (HPAs) family. They are widely used as catalysts due to their high Brønsted acidity, and their dispersion on solid supports favors the accessibility to their acid sites generally increasing the catalytic activity. A series of binary materials composed of Keggin or Wells–Dawson HPAs and SiO2, TiO2, and ZrO2 have been prepared by impregnation or solvothermal methods. Remarkable differences have been found in the catalytic activities among the unsupported and supported HPAs. These differences have been correlated in the past to the structural changes of the HPAs due to the cluster–support interaction, which is different depending on preparation methodologies of the binary material. In the present work, the modes of interaction between the two types of HPA, Keggin and Wells–Dawson, and various supports have been studied by X-ray absorption spectroscopy. The obtained data have been compared to the characterization of the same materials reported before by using different bulk and surface physicochemical techniques. The characterization results were then used to correlate the interaction modes between the HPAs and the supports with the catalytic performances reported for 2-propanol dehydration to propene and for propene hydration to 2-propanol. The results reveal that the deposition of HPA by impregnation or solvothermal treatment may cause distortions in the H3PW12O40 cluster structure depending on the presence of stronger (TiO2 and ZrO2) or weaker (SiO2) basic sites in the support, respectively. Moreover, the type of preparation method affects the structure and acidic properties of the supported HPAs. In particular, during the preparation of TiO2 and ZrO2 with HPA by in situ solvothermal method, the reaction of the HPA with the products of metal alkoxides hydrolysis occurs with consequent destruction of the Keggin structur

Phenylalanine hydroxylase (PAH) is a key enzyme in the catabo-lism of phenylalanine, and mutations in this enzyme cause phenylketonuria (PKU), a genetic disorder that leads to brain damage and mental retardation if untreated. Some patients benefit from supplementation with a synthetic formulation of the cofactor tetrahydrobiopterin (BH) that partly acts as a pharmacological chaperone. Here we present structures of full-length human PAH (hPAH) both unbound and complexed with BH in the precatalytic state. Crystal structures, solved at 3.18-Å resolution, show the interactions between the cofactor and PAH, explaining the negative regulation exerted by BH. BH forms several H-bonds with the N-terminal autoregulatory tail but is far from the catalytic Fe. Upon BH binding a polar and salt-bridge interaction network links the three PAH domains, explaining the stability conferred by BH. Importantly, BH binding modulates the interaction between subunits, providing information about PAH allostery. Moreover, we also show that the cryo-EM structure of hPAH in absence of BH reveals a highly dynamic conformation for the tetramers. Structural analyses of the hPAH:BH subunits revealed that the substrate-induced movement of Tyr138 into the active site could be coupled to the displacement of BH from the precatalytic toward the active conformation, a molecular mechanism that was supported by site-directed mutagenesis and targeted molecular dynamics simulations. Finally, comparison of the rat and human PAH structures show that hPAH is more dynamic, which is related to amino acid substitutions that enhance the flexibility of hPAH and may increase the susceptibility to PKU-associated mutations.

Fungal cell wall synthesis is achieved by a balance of glycosyltransferase, hydrolase and transglycosylase activities. Transglycosylases strengthen the cell wall by forming a rigid network of crosslinks through mechanisms that remain to be explored. Here we study the function of the Aspergillus fumigatus family of five Crh transglycosylases. Although crh genes are dispensable for cell viability, simultaneous deletion of all genes renders cells sensitive to cell wall interfering compounds. In vitro biochemical assays and localisation studies demonstrate that this family of enzymes functions redundantly as transglycosylases for both chitin-glucan and chitin-chitin cell wall crosslinks. To understand the molecular basis of this acceptor promiscuity, we solved the crystal structure of A. fumigatus Crh5 (AfCrh5) in complex with a chitooligosaccharide at the resolution of 2.8 Å, revealing an extensive elongated binding cleft for the donor (−4 to −1) substrate and a short acceptor (+1 to +2) binding site. Together with mutagenesis, the structure suggests a “hydrolysis product assisted” molecular mechanism favouring transglycosylation over hydrolysis.

[EN] NiO and metal-promoted NiO catalysts (M-NiO, with a M/(M+Ni) atomic ratio of 0.08, with M = Nb, Sn, or La) have been prepared, tested in the oxidative dehydrogenation (ODH) of ethane, and characterized by means of XRD, TPR, HRTEM, Raman, XPS, and in situ XAS (using H-2/He, air or C2H6/He mixtures). The selectivity to ethylene during the ODH of ethane decreases according to the following trend: Nb NiO Sn NiO > La NiO > NiO, whereas the catalyst reducibility (determined by both TPR and XAS using H-2/He mixtures) shows the opposite trend. However, different reducibility and catalytic behavior in the absence of oxygen (ethane/He mixtures) have been observed, especially when comparing Nb- and Sn-promoted NiO samples. These differences can be ascribed mainly to a different phase distribution of the promoter. The results presented here are discussed in terms of the nature of active and selective sites for ODH of ethane in selective and unselective catalysts, but also the role of promoters and the importance of their phase distribution.

Enduring host-microbiome relationships are based on adaptive strategies within a particular ecological niche. Tannerella forsythia is a dysbiotic member of the human oral microbiome that inhabits periodontal pockets and contributes to chronic periodontitis. To counteract endopeptidases from the host or microbial competitors, T. forsythia possesses a serpin-type proteinase inhibitor called miropin. Although serpins from animals, plants, and viruses have been widely studied, those from prokaryotes have received only limited attention. Here we show that miropin uses the serpin-type suicidal mechanism. We found that, similar to a snap trap, the protein transits from a metastable native form to a relaxed triggered or induced form after cleavage of a reactive-site target bond in an exposed reactive-center loop. The prey peptidase becomes covalently attached to the inhibitor, is dragged 75 Å apart, and is irreversibly inhibited. This coincides with a large conformational rearrangement of miropin, which inserts the segment upstream of the cleavage site as an extra-strand in a central-sheet. Standard serpins possess a single target bond and inhibit selected endopeptidases of particular specificity and class. In contrast, miropin uniquely blocked many serine and cysteine endopeptidases of disparate architecture and substrate specificity owing to several potential target bonds within the reactive-center loop and to plasticity in accommodating extra -strands of variable length. Phylogenetic studies revealed a patchy distribution of bacterial serpins incompatible with a vertical descent model. This finding suggests that miropin was acquired from the host through horizontal gene transfer, perhaps facilitated by the long and intimate association of T. forsythia with the human gingiva

Variolin B is a rare marine alkaloid that showed promising anti-cancer activity soon after its isolation. It acts as a cyclin-dependent kinase inhibitor, although the precise mechanism through which it exerts the cytotoxic effects is still unknown. The crystal structure of a variolin B bound to a DNA forming a pseudo-Holliday junction shows that this compound can also contribute, through intercalative binding, to either the formation or stabilization of multi-stranded DNA forms.

Membrane fusion is essential in a myriad of eukaryotic cell biological processes, including the synaptic transmission. Rabphilin-3A is a membrane trafficking protein involved in the calcium-dependent regulation of secretory vesicle exocytosis in neurons and neuroendocrine cells, but the underlying mechanism remains poorly understood. Here, we report the crystal structures and biochemical analyses of Rabphilin-3A C2B–SNAP25 and C2B–phosphatidylinositol 4,5-bisphosphate (PIP2) complexes, revealing how Rabphilin-3A C2 domains operate in cooperation with PIP2/Ca2+ and SNAP25 to bind the plasma membrane, adopting a conformation compatible to interact with the complete SNARE complex. Comparisons with the synaptotagmin1–SNARE show that both proteins contact the same SNAP25 surface, but Rabphilin-3A uses a unique structural element. Data obtained here suggest a model to explain the Ca2+-dependent fusion process by membrane bending with a myriad of variations depending on the properties of the C2 domain-bearing protein, shedding light to understand the fine-tuning control of the different vesicle fusion events.

High-efficiency kesterite-based thin film solar cells typically feature Cu-poor, Zn-rich absorbers although secondary phases occur easily in non-stoichiometric CuZnSnSe. We therefore applied high-resolution X-ray fluorescence analysis using a synchrotron nanobeam to study the local composition of a CZTSe cross section lamella cut from a sample with an integral composition of Zn/Sn = 1.37 and Cu/(Zn+Sn) = 0.55. We find submicrometer-sized ZnSe-, SnSe/SnSe-, and even CuSe/CuSe-like secondary phases, while the local compositions of the kesterite are highly Zn-rich yet barely Cu-poor with 1.5 ≤ Zn/Sn ≤ 2.2 and Cu/(Zn+Sn) ∼ 1.0. Consequently, great care must be taken when relating the integral composition to other material properties including the device performance.

In this work, thin magnetite films were deposited on SrTiO3 via reactive molecular beam epitaxy at different substrate temperatures. The growth process was monitored in-situ during deposition by means of x-ray diffraction. While the magnetite film grown at 400 C shows a fully relaxed vertical lattice constant already in the early growth stages, the film deposited at 270 C exhibits a strong vertical compressive strain and relaxes towards the bulk value with increasing film thickness. Furthermore, a lateral tensile strain was observed under these growth conditions although the inverse behavior is expected due to the lattice mismatch of 7.5%. Additionally, the occupancy of the A and B sublattices of magnetite with tetrahedral and octahedral sites was investigated showing a lower occupancy of the A sites compared to an ideal inverse spinel structure. The occupation of A sites decreases for a higher growth temperature. Thus, we assume a relocation of the iron ions from tetrahedral sites to octahedral vacancies forming a deficient rock salt lattice.

In this study we analyze in detail a palygorskite from Palygorskaja. This palygorskite is situated in the context of the existing studies using X-ray powder diffraction analysis. Moreover, a novel microdiffraction study on a small bunch of fibers shows highly structured 2D diffraction patterns that allow to decipher some information on the microstructure, thus overcoming the uncertainty usually originated by large samples containing mixtures and impurities. Structural data provided by Chisholm (1992) are used to simulate 1D and 2D powder and fiber diffraction patterns for palygorskite, which are compared with the experimental results. We performed simulations for powder and fiber diffraction and we centered our attention in the region of interest with d-spacings between 4.0 and 4.5 Å. This palygorskite is consistent with a purely orthorhombic palygorskite, based on good agreement of data with simulations. The experimental results present some reflections not found in the simulations. These reflections are interpreted as corresponding to other hk1 planes of palygorskite. They do not match any reflection from the monoclinic structural model nor from probable impurities, reinforcing the interpretation of them being intrinsic to the structure of the mineral. Our findings suggest a revisal of the commonly accepted structure of palygorskite. They correspond to hk1 planes of palygorskite, and they do not match any reflection neither from the monoclinic structural model nor from possible impurities, and thus reinforcing the idea of them being intrinsic to the structure of the mineral, suggesting the necessity of a revisal of the commonly accepted structure of palygorskite.

Recent studies reveal that the mechanical properties of virus particles may have been shaped by evolution to facilitate virus survival. Manipulation of the mechanical behavior of virus capsids is leading to a better understanding of viral infection, and to the development of virus-based nanoparticles with improved mechanical properties for nanotechnological applications. In the minute virus of mice (MVM), deleterious mutations around capsid pores involved in infection-related translocation events invariably increased local mechanical stiffness and interfered with pore-associated dynamics. To provide atomicresolution insights into biologically relevant changes in virus capsid mechanics, we have determined by X-ray crystallography the structural effects of deleterious, mechanically stiffening mutations around the capsid pores. Data show that the cavity-creating N170A mutation at the pore wall does not induce any dramatic structural change around the pores, but instead generates subtle rearrangements that propagate throughout the capsid, resulting in a more compact, less flexible structure. Analysis of the spacefilling L172W mutation revealed the same relationship between increased stiffness and compacted capsid structure. Implications for understanding connections between virus mechanics, structure, dynamics and infectivity, and for engineering modified virus-based nanoparticles, are discussed

The association-dissociation of the cap-binding protein eukaryotic translation initiation factor 4E (eIF4E) with eIF4G is a key control step in eukaryotic translation. The paradigm on the eIF4E-eIF4G interaction states that eIF4G binds to the dorsal surface of eIF4E through a single canonical alpha-helical motif, while metazoan eIF4E-binding proteins (m4E-BPs) advantageously compete against eIF4G via bimodal interactions involving this canonical motif and a second noncanonical motif of the eIF4E surface. Metazoan eIF4Gs share this extended binding interface with m4E-BPs, with significant implications on the understanding of translation regulation and the design of therapeutic molecules. Here we show the high-resolution structure of melon (Cucumis melo) eIF4E in complex with a melon eIF4G peptide and propose the first eIF4E-eIF4G structural model for plants. Our structural data together with functional analyses demonstrate that plant eIF4G binds to eIF4E through both the canonical and noncanonical motifs, similarly to metazoan eIF4E-eIF4G complexes. As in the case of metazoan eIF4E-eIF4G, this may have very important practical implications, as plant eIF4E-eIF4G is also involved in a significant number of plant diseases. In light of our results, a universal eukaryotic bipartite mode of binding to eIF4E is proposed.

Epitaxial iron oxide layers with different orientations were grown on Ag(001) surface by choosing the appropriate preparation conditions. A film with a hexagonal surface mesh interpreted as (111)-oriented magnetite was formed by reactive deposition of iron in molecular oxygen at room temperature (RT), followed by annealing in UHV. Instead, highly ordered epitaxial layers with P4m symmetry were obtained by a three-step process, optimized through in situ experiments. Following this method, an ultrathin Fe layer was first grown in coherent epitaxy on the substrate and then dosed twice with O2, first at RT and next during annealing. A structural analysis combining low-energy electron diffraction, scanning tunneling microscopy, and accurate surface x-ray diffraction measurements confirmed that these films consist of (001)-oriented magnetite, although with a slight tetragonal distortion induced by the substrate constraints. Both its surface and interface are atomically sharp, an essential requirement for its integration into spintronic based devices.

By using a combination of heteroepitaxial growth, structure refinement based on synchrotron x-ray diffraction, and first-principles calculations, we show that the symmetry-protected Dirac line nodes in the topological semimetallic perovskite SrIrO3 can be lifted simply by applying epitaxial constraints. In particular, the Dirac gap opens without breaking the Pbnm mirror symmetry. In virtue of a symmetry-breaking analysis, we demonstrate that the original symmetry protection is related to the n-glide operation, which can be selectively broken by different heteroepitaxial structures. This symmetry protection renders the nodal line a nonsymmorphic Dirac semimetallic state. The results highlight the vital role of crystal symmetry in spin-orbit-coupled correlated oxides and provide a foundation for experimental realization of topological insulators in iridate-based heterostructures.

We describe the conditions for optimal formation of laser-induced periodic surface structures (LIPSS) over poly(3-hexylthiophene) (P3HT) spin-coated films. Optimal LIPSS on P3HT are observed within a particular range of thicknesses and laser fluences. These conditions can be translated to the photovoltaic blend formed by the 1:1 mixture of P3HT and [6,6]-phenyl C-butyric acid methyl ester (PCBM) when deposited on an indium tin oxide (ITO) electrode coated with (poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS). Solar cells formed by using either a bilayer of P3HT structured by LIPSS covered by PCBM or a bulk heterojunction with a P3HT:PCBM blend structured by LIPSS exhibit generation of electrical photocurrent under light illumination. These results suggest that LIPSS could be a compatible technology with organic photovoltaic devices. Copyright © 2016 American Chemical Society

A family of interwoven molecular inorganic knots, shaped like the 'Star of David', was prepared by the employment of naphthalene-2,3-diol in 3d/4f-metal cluster chemistry; the isoskeletal dodecanuclear compounds exhibit slow relaxation of the magnetization and magnetocaloric properties, depending on the metal ion.

Catalytically inactive oxidized O2-sensitive [NiFe]-hydrogenases are characterized by a mixture of the paramagnetic Ni-A and Ni-B states. Upon O2 exposure, enzymes in a partially reduced state preferentially form the unready Ni-A state. Because partial O2 reduction should generate a peroxide intermediate, this species was previously assigned to the elongated Ni–Fe bridging electron density observed for preparations of [NiFe]-hydrogenases known to contain the Ni-A state. However, this proposition has been challenged based on the stability of this state to UV light exposure and the possibility of generating it anaerobically under either chemical or electrochemical oxidizing conditions. Consequently, we have considered alternative structures for the Ni-A species including oxidation of thiolate ligands to either sulfenate or sulfenic acid. Here, we report both new and revised [NiFe]-hydrogenases structures and conclude, taking into account corresponding characterizations by Fourier transform infrared spectroscopy (FTIR), that the Ni-A species contains oxidized cysteine and bridging hydroxide ligands instead of the peroxide ligand we proposed earlier. Our analysis was rendered difficult by the typical formation of mixtures of unready oxidized states that, furthermore, can be reduced by X-ray induced photoelectrons. The present study could be carried out thanks to the use of Desulfovibrio fructosovorans [NiFe]-hydrogenase mutants with special properties. In addition to the Ni-A state, crystallographic results are also reported for two diamagnetic unready states, allowing the proposal of a revised oxidized inactive Ni-SU model and a new structure characterized by a persulfide ion that is assigned to an Ni-‘Sox’ species.

© 2015 American Chemical Society. In this work, we report on the surface patterning of semiconducting poly(3-hexylthiophene) (P3HT) thin films by means of laser-induced periodic surface structures (LIPSS). Two different laser wavelengths, 266 and 532 nm, and a broad range of fluences and number of pulses have been used in order to optimize the LIPSS morphology. Ripples period and depth can be tuned by laser parameters. In particular, the high optical absorption of P3HT at 532 nm enables the formation of well-ordered nanostructures with periodicities around 460 nm. Near edge X-ray absorption fine structure (NEXAFS) and Raman spectroscopy reveal a good chemical stability of P3HT thin films during LIPSS formation. Conducting atomic force microscopy (C-AFM) performed on the LIPSS reveals a higher electrical conduction in the trenches than in the ridge regions. Resonance Raman spectroscopy and grazing incidence wide-angle X-ray scattering (GIWAXS) indicate a loss of crystallinity of P3HT thin films during LIPSS formation, suggesting melting of the outer polymer surface. This effect produces ridges with molecular order lower than that of the original thin film. As a consequence of this transformation, the electrical conduction in the ridges becomes lower than that in the trenches.

In this work we have developed an efficient projector for laboratory based, polychromatic cone beam diffraction imaging. Using this projector, the three-dimensional shape of grains with negligible intra-granular orientation gradient can be reconstructed using iterative, algebraic reconstruction techniques (e.g. SIRT). The reconstructions show a clear improvement compared to the previously used processing route, based on a regular cone beam projector and affine transformation of the projection images. With further improvement of polycrystalline indexing algorithms and with extension to a 6D reconstruction framework, we anticipate LabDCT to become a true alternative to established synchrotron techniques. The combination of absorption (detection of damage, second phases, porosity, plastic strain via 3D digital volume correlation techniques) and diffraction imaging (crystal shape and orientation, elastic strain) on the same instrument will provide unique possibilities for (interrupted) in-situ characterization of dynamic processes in the bulk of polycrystalline materials (e.g. grain coarsening during heat treatment, plastic deformation and damage mechanisms, etc.)., The original document contains color images.

Functional lung CT using synchrotron radiation was applied for studying regional ventilation distribution in vivo in animal lungs. This quantitative method employs the K-edge subtraction (KES) technique, which takes advantage of the sharp rise of the absorption coefficient at the binding energy of K-shell electron of a contrast agent. In KES technique two images are taken simultaneously at energies bracketing the K-edge energy of stable xenon (Xe) gas. This technique produces absorption CT images for structural evaluation and Xe density images and at the same time it allows the study of the regional ventilation heterogeneity, calculated based on wash-in series of Xe inhalation images. In this work the analysis of KES CT images was developed to show the regional differences in the airway reactions produced by the direct constrictor agonist, methacholine (MCh), and the indirect constrictor agonist, ovalbumin (OVA), in healthy and asthmatic rabbits. Moreover these constrictors were tested under the influence of cigarette smoke. The effect in airways of different administration routes of MCh, inhaled or intravenous (i.v.), was studied using low radiation dose Xe density CT images. The radiation dose in synchrotron radiation imaging of rabbit lungs in vivo, with and without Xe, was calculated and measured using several methods and compared to the image quality. Results showed that i.v. MCh caused bronchoconstriction primarily in central airways in healthy and asthmatic animals, whereas i.v. OVA only in asthmatic animals. Inhaled MCh, in both groups, affected more the periphery. On the other hand cigarette smoke inhibited the bronchoconstriction in both healthy and asthmatic animals. Theoretical and measured values of synchrotron radiation dose were consistent in this setup. Dose dependency of the image quality, defined by signal to noise ratio, was evaluated, and a threshold for detectable signal contrast was found. The optimal imaging setup was estimated using these res, Astma on yleinen sairaus teollisissa maissa ja Suomessa siihen sairastuu noin 9 % väestöstä. Astmassa keuhkojen alueellinen toiminta on häiriintynyttä. Perinteisesti keuhkojen toimintaa on tutkittu spirometrialla tai radionuklidimenetelmillä, joiden erotuskyky tai kvantitatiivisuus eivät ole riittäviä paikantamaan keuhkojen ääreisosien toimintaa tai rakennetta. Keuhkojen toimintaa voidaan tutkia aiempaa tarkemmin synkrotronilla tuotettuun röntgensäteilyyn perustuvalla funktionaalisella tietokonetomografialla (TT), joka perustuu kontrastiaineen, xenonin, K-reunan vähennystekniikkaan (KES). Tekniikalla voidaan tuottaa samanaikaisesti sekä perinteisiä TT-kuvia keuhkorakenteen tutkimiseen että xenonin tiheyskuvia, joista saadaan kvantitatiivista tietoa kuten absoluuttisia tiheyksiä tai hengityskuvia paikallisen keuhkotuuletuksen määrittämiseen. Väitöskirjatyössä KES-TT analyysiä kehitettiin määrittämään keuhkojen toiminnan paikallisia muutoksia astmankaltaisessa tai allergeenin aiheuttamassa reaktiossa terveillä ja astmaattisilla kaneilla. Myös tupakansavun vaikutusta näihin reaktioihin testattiin. Lisäksi tutkittiin suonensisäisesti annetun tai hengitetyn astmareaktiota aiheuttavan lääkkeen vaikutuksen eroa keuhkojen toimintaan. Kuvauksessa käytetyn synkrotronisäteilyn annos määritettiin sekä teoreettisesti että mittaamalla. Säteilyannoksen ja kuvanlaadun keskinäistä riippuvuutta tutkittiin. Löydösten perusteella KES-TT menetelmän avulla voidaan tutkia sekä funktionaalisesti keuhkojen tuuletuksen jakautumista ja sen muutoksia paikallisesti että saada tietoa keuhkojen anatomiasta. Kehittämällä laitteistoa ja optimoimalla rekonstruktioalgoritmit on mahdollista soveltaa KES-TT tekniikkaa myös ihmiskeuhkojen kuvaukseen.

In the coronavirus (CoV), the envelope spike (S) glycoprotein is responsible for CoV cell entry and host-to-host transmission. The S is a multifunctional glycoprotein that mediates both attachment of CoV particles to cell surface receptor molecules as well as membrane penetration by fusion. Receptor-binding domains (RBD) have been identified in the S of diverse CoV; they usually contain antigenic determinants targeted by antibodies that neutralize CoV infections. To penetrate host cells, the CoV can use various cell surface molecules, although they preferentially bind to ectoenzymes. Several crystal structures have determined the folding of CoV RBD and the mode by which they recognize cell entry receptors. Here we review the CoV-receptor complex structures reported to date, and highlight the distinct receptor recognition modes, common features, and key determinants of the binding specificity. Structural studies have established the basis for understanding receptor recognition diversity in CoV, its evolution and the adaptation of this virus family to different hosts. CoV responsible for recent outbreaks have extraordinary potential for cross-species transmission; their RBD bear large platforms specialized in recognition of receptors from different species, which facilitates host-to-host circulation and adaptation to man.

The interdependence between training and magnetization reversal in granular Co-CoO exchange bias (EB) systems prepared by O ion implantation in Co thin films is demonstrated by polarized neutron reflectometry. While high-fluence O-implanted thin films show reduced relative training values and no asymmetry in magnetization reversal (all reversals take place by domain wall nucleation and motion), low-fluence O ion implantation results in an increased relative training and a magnetization reversal asymmetry between the first descending and the first ascending branches. Whereas the untrained decreasing field reversal occurs mainly by domain wall nucleation and motion, traces of a domain rotation contribution are evidenced in the increasing field reversal. This is explained by the evolution of the CoO structure and the contribution of the out-of-plane magnetization with ion implantation. The amount of incorporated O, which determines the threshold between both behaviors, is around 20 at.%. This reveals that the interdependence between training and magnetization reversal is insensitive to the morphology of the constituents (i.e., granular or layered), indicating that this is an intrinsic EB effect, which can be conveniently tailored by the interplay between the intrinsic properties of the investigated materials and ion implantation.

The spin state of organic-based magnets at interfaces is to a great extent determined by the organic environment and the nature of the spin-carrying metal center, which is further subject to modifications by the adsorbate-substrate coupling. Direct chemical doping offers an additional route for tailoring the electronic and magnetic characteristics of molecular magnets. Here we present a systematic investigation of the effects of alkali metal doping on the charge state and crystal field of 3d metal ions in Cu, Ni, Fe, and Mn phthalocyanine (Pc) monolayers adsorbed on Ag. Combined X-ray absorption spectroscopy and ligand field multiplet calculations show that Cu(II), Ni(II), and Fe(II) ions reduce to Cu(I), Ni(I), and Fe(I) upon alkali metal adsorption, whereas Mn maintains its formal oxidation state. The strength of the crystal field at the Ni, Fe, and Mn sites is strongly reduced upon doping. The combined effect of these changes is that the magnetic moment of high- and low-spin ions such as Cu and Ni can be entirely turned off or on, respectively, whereas the magnetic configuration of MnPc can be changed from intermediate (3/2) to high (5/2) spin. In the case of FePc a 10-fold increase of the orbital magnetic moment accompanies charge transfer and a transition to a high-spin state. © 2014 American Chemical Society.

A challenge for microbial pathogens is to assure that their translocated effector proteins target only the correct host cell compartment during infection. The Legionella pneumophila effector vacuolar protein sorting inhibitor protein D (VipD) localizes to early endosomal membranes and alters their lipid and protein composition, thereby protecting the pathogen from endosomal fusion. This process requires the phospholipase A1 (PLA1) activity of VipD that is triggered specifically on VipD binding to the host cell GTPase Rab5, a key regulator of endosomes. Here, we present the crystal structure of VipD in complex with constitutively active Rab5 and reveal the molecular mechanism underlying PLA1 activation. An active site-obstructing loop that originates from the C-terminal domain of VipD is repositioned on Rab5 binding, thereby exposing the catalytic pocket within the N-terminal PLA1 domain. Substitution of amino acid residues located within the VipD–Rab5 interface prevented Rab5 binding and PLA1 activation and caused a failure of VipD mutant proteins to target to Rab5-enriched endosomal structures within cells. Experimental and computational analyses confirmed an extended VipD-binding interface on Rab5, explaining why this L. pneumophila effector can compete with cellular ligands for Rab5 binding. Together, our data explain how the catalytic activity of a microbial effector can be precisely linked to its subcellular localization.

The respiratory pathogen Streptococcus pneumoniae has evolved efficient mechanisms to resist oxidative stress conditions and to displace other bacteria in the nasopharynx. Here we character ize at physiological, functional and structural levels two novel surface-exposed thioredoxin-family lipoproteins, Etrx1 and Etrx2. The impact of both Etrx proteins and their r edox partner methionine sulfoxide reductase SpMsrAB2 on pneumococcal pathogenesis was assessed in mouse virulence studies and phagocytosis assays. The results demonstrate that loss of function of either both Etrx proteins or SpMsrAB2 dramatically attenuated pneumococcal virulence in the acute mouse pneumonia model and that Etrx proteins compensate each other. The deficiency of Etrx proteins or SpMsrAB2 further enhanced bacterial uptake by macrophages, and accelerated pneumococcal killing by H2O2 or free methionine sulfoxides (MetSO). Moreover, the absence of both Etrx redox pathways provokes an accumulation of oxidized SpMsrAB2 in vivo. Taken together our results reveal insights into the role of two extracellular electron pathways required for reduction of SpMsrAB2 and surface-exposed MetSO. Identification of this system and its target proteins paves the w ay for the design of novel a ntimicrobials

The behaviour of the Pd phase in three way catalysts (TWCs) having a Ce-Zr oxide as a promoter component has been examined under CO/NO cycling conditions. In order to extract information on the role of the noble metal and the metal-promoter interface, two catalysts in, respectively, the presence or the absence of the promoter and having a similar Pd particle size were analyzed by a synchronous multitechnique approach using X-ray absorption (XAS) or high energy X-ray diffraction (HXRD) in combination with diffuse reflectance Fourier transform infrared spectroscopy (DRIFTS) and mass spectrometry (MS). From a structural point of view it is shown that the promoter oxide strongly influences Pd behaviour, limiting morphological (size/shape) and structural (formation of carbide/oxide phases) modifications occurring under dynamic conditions in the absence of the promoter. Activity measurements show that these phenomena have important chemical consequences in terms of CO/NO pollutant metal coverage(s), the occurrence of NO and/or CO dissociation steps as well as the subsequent transformation of the pollutants into CO2 and N2.

We have performed a deep spectroscopic study of incommensurate satellite reflections (h, k, l) ± (0,0.278, 0) on a TbMnO3 single crystal in order to shed light on its physical origin. Resonant x-ray scattering experiments at the Mn K-edge and Tb L3-edge have been performed at different temperatures and azimuthal angles, analyzing the outgoing light polarization. Our experimental results agree with a magnetic origin for A and C-type reflections, while F and G-type have the hallmarks of anisotropic tensor susceptibility (ATS) reflections, so that they come purely from the structural modulation.

Structural and electronic properties of TbMn1-xCoxO3 samples have been characterized by means of x-ray and neutron diffraction and x-ray absorption spectroscopic techniques. Crystallographic structure was refined from diffraction data, and samples show the orthorhombic distorted perovskite structure (Pbnm), being isostructural to TbMnO3, except for x=0.4, 0.5 and 0.6, where an ordered double perovskite structure (P21/n) is found. The electronic configuration of Mn and Co ions was obtained along the series from the chemical shift of the edge on x-ray absorption spectra, at the Mn and Co K-edges. Our results agree with a charge redistribution between Mn and Co ions, yielding a mixed valence state Mn3+/Mn4+ and Co3+/Co2+ for the whole series.

This work studies the effects of copper doping on the properties of the (K0.44Na0.52Li0.04)(Nb0.86Ta 0.10Sb0.04)O3 piezoelectric ceramic material. Cu2+ incorporation into the perovskite structure produces a transformation of the crystalline lattice from tetragonal to orthorhombic symmetry together with an increase of the secondary phase. The grain size of the ceramic samples is increased due to the formation of a liquid phase during sintering, which increases with the Cu2+ content. EDS analysis reveals that the secondary-phase regions present a Cu and Nb-rich composition, indicating that the Cu-excess accommodates through the formation of this secondary phase. Cu-doping induces a rapid increase of the orthorhombic- tetragonal phase transition temperature, while the tetragonal-cubic phase transition temperature is decreased, the latter becoming more diffuse with the increase of Cu content. The piezoelectric properties of the material are reduced with the copper concentration, whereas the mechanical quality factor increases by a factor of nearly four. © 2012 Elsevier Ltd and Techna Group S.r.l.

Inositol phosphates (InsPs) are signaling molecules with multiple roles in cells. In particular Ins(1,2,3,4,5,6)P6 (InsP6) is involved in mRNA export and editing or chromatin remodeling among other events. InsP6 accumulates as mixed salts (phytate) in storage tissues of plants and plays a key role in their physiology. Human diets that are exclusively grain-based provide an excess of InsP6 that, through chelation of metal ions, may have a detrimental effect on human health. Ins(1,3,4,5,6)P5 2-kinase (InsP5 2-kinase or Ipk1) catalyses the synthesis of InsP6 from InsP5 and ATP, and is the only enzyme that transfers a phosphate group to the axial 2-OH of the myo-inositide. We present the first structure for an InsP5 2-kinase in complex with both substrates and products. This enzyme presents a singular structural region for inositide binding that encompasses almost half of the protein. The key residues in substrate binding are identified, with Asp368 being responsible for recognition of the axial 2-OH. This study sheds light on the unique molecular mechanism for the synthesis of the precursor of inositol pyrophosphates.

The structural and magnetic properties of 1.8 nm Co particles dispersed in a Mn matrix by co-depositing pre-formed mass-selected Co clusters with an atomic vapour of Mn onto a common substrate have been studied by using EXAFS (extended x-ray absorption fine structure), XMCD (x-ray magnetic circular dichroism), magnetometry, and theoretical modelling. At low Co volume fraction (5%) Co@Mn shows a significant degree of alloying and the well-defined particles originally deposited become centres of high Co concentration CoMn alloy that evolves from pure Co at the nanoparticle centre to the pure Mn matrix within a few nm. Each inhomogeneity is a core-shell particle with a Co-rich ferromagnetic core in contact with a Co-depleted antiferromagnetic shell. The XMCD reveals that the Co moment localized on the Co atoms within the Co-rich cores is much smaller than the ferromagnetic moment of the Co nanoparticles deposited at the same volume fraction in Ag. Electronic structure calculations indicate that the small magnitude of the core Co moment can be understood only if significant alloying occurs. Monte Carlo modelling replicates the exchange bias (EB) behaviour observed at low temperature from magnetometry measurements. We ascribe EB to the interaction between the ferromagnetic Co-rich cores and the antiferromagnetic Mn-rich shells.

The physical properties of many multiphase systems are determined by coarsening phenomena. From raindrops to polycrystal grains and foams, the formation and stability of these systems continuously evolve towards lower-energy configurations through events such as coalescence, Ostwald ripening and drainage. Here we propose a procedure to identify and characterise key topological transformations of coarsening phenomena using a physically-based fluid dynamic framework. In situ, real-time foaming processes of a polymeric matrix reinforced with two morphologically different nanofillers, carbon nanotubes and graphene sheets were observed by synchrotron X-ray radioscopy. We obtained detailed information on the evolution of the growth patterns and coarsening events. Filled samples showed differences in both trend and speed compared with the unfilled sample. Furthermore, we found different dominating coarsening phenomena due to the wetting nature of carbon nanoparticles. Our procedure can be extended to sequences of any type of 2D projection or 3D images and to other multiphase systems. © the Owner Societies 2009.

RNA virus replication is an error-prone event caused by the low fidelity of viral RNA-dependent RNA polymerases. Replication fidelity can be decreased further by the use of mutagenic ribonucleoside analogs to a point where viral genetic information can no longer be maintained. For foot-and-mouth disease virus, the antiviral analogs ribavirin and 5-fluorouracil have been shown to be mutagenic, contributing to virus extinction through lethal mutagenesis. Here, we report the x-ray structure of four elongation complexes of foot-and-mouth disease virus polymerase 3D obtained in presence of natural substrates, ATP and UTP, or mutagenic nucleotides, ribavirin triphosphate and 5-fluorouridine triphosphate with different RNAs as template-primer molecules. The ability of these complexes to synthesize RNA in crystals allowed us to capture different successive replication events and to define the critical amino acids involved in (i) the recognition and positioning of the incoming nucleotide or analog; (ii) the positioning of the acceptor base of the template strand; and (iii) the positioning of the 3′-OH group of the primer nucleotide during RNA replication. The structures identify key interactions involved in viral RNA replication and provide insights into the molecular basis of the low fidelity of viral RNA polymerases. © 2007 by The National Academy of Sciences of the USA.

We have employed time-resolved X-ray diffraction with picosecond temporal resolution to measure the time-dependent rocking curves of laser-irradiated asymmetrically cut single InSb crystals. Coherent acoustic phonons were excited in the crystals by irradiation with 800-nm, 100-fs laser pulses at irradiances between 0.25 and 12??mJ/cm 2 . The induced time-dependent strain profiles (corresponding to the coherent phonons) were monitored by diffracting collimated, monochromatic pulses of X-rays from the irradiated crystals. Recording of the diffracted radiation with a fast low-jitter X-ray streak camera resulted in an overall temporal resolution of better than 2??ps. The strain associated with the coherent phonons modifies the rocking curve of the crystal in a time-dependent manner, and the rocking curve is recorded by keeping the angle of incidence of the X-rays upon the crystal fixed, but varying the energy of the incident X-rays around a central energy of 8.453??keV (corresponding to the peak of the rocking curve of the unperturbed crystal). The observed time-dependent diffraction from the irradiated crystals is in reasonable agreement with simulations over a wide range of energies from the unperturbed rocking-curve peak.

In situ> conductivity measurements on Al-Pd-Mn quasicrystals have been combined with synchrotron x-ray-diffraction experiments for studying its behavior during phase transformations. In order to confidently reduce the possible contribution to the conductivity of defects and grain boundaries, single-crystal samples have been annealed in situ under UHV conditions. This combined experiment allows us to affirm unambiguously that the structural state of the i-Al-Pd-Mn single crystal influences the electrical conductivity. ©2003 American Physical Society

This article is from 'Physics of X-Ray Multilayer Structures' AD-A255 383, p16-19.

International audience, ID24 is the energy dispersive beamline of the European Synchrotron Radiation Facility dedicated to X-ray Absorption Spectroscopy (XAS). Since 2000, a complete refurbishment program has started, including source upgrade, mirrors replacement, polychromator optimization and detection improvements. These have made possible the development of new applications in a variety of different fields, ranging from the measurement of tiny atom displacements to time resolved techniques, from measurements under extreme conditions to micro-XAS studies.