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With the increasing incidence of oral cancer in the world, it has become a hotspot to explore the pathogenesis and prevention of oral cancer. It has been proved there is a strong link between periodontal pathogens and oral cancer. However, the specific molecular and cellular pathogenic mechanisms remain to be further elucidated. Emerging evidence suggests that periodontal pathogens‐induced epithelial–mesenchymal transition (EMT) is closely related to the progression of oral cancer. Cells undergoing EMT showed increased motility, aggressiveness and stemness, which provide a pro‐tumour environment and promote malignant metastasis of oral cancer. Plenty of studies proposed periodontal pathogens promote carcinogenesis via EMT. In the current review, we discussed the association between the development of oral cancer and periodontal pathogens, and summarized various mechanisms of EMT caused by periodontal pathogens, which are supposed to play an important role in oral cancer, to provide targets for future research in the fight against oral cancer. [ABSTRACT FROM AUTHOR]

A series of isostructural Ln3O2(CN3) (Ln=La, Eu, Gd, Tb, Ho, Yb) oxoguanidinates was synthesized under high‐pressure (25–54 GPa) high‐temperature (2000–3000 K) conditions in laser‐heated diamond anvil cells. The crystal structure of this novel class of compounds was determined via synchrotron single‐crystal X‐ray diffraction (SCXRD) as well as corroborated by X‐ray absorption near edge structure (XANES) measurements and density functional theory (DFT) calculations. The Ln3O2(CN3) solids are composed of the hitherto unknown CN35− guanidinate anion—deprotonated guanidine. Changes in unit cell volumes and compressibility of Ln3O2(CN3) (Ln=La, Eu, Gd, Tb, Ho, Yb) compounds are found to be dictated by the lanthanide contraction phenomenon. Decompression experiments show that Ln3O2(CN3) compounds are recoverable to ambient conditions. The stabilization of the CN35− guanidinate anion at ambient conditions provides new opportunities in inorganic and organic synthetic chemistry. [ABSTRACT FROM AUTHOR]

Porphyromonas gingivalis (P. gingivalis) is a pivotal pathogen of periodontitis. Our previous studies have confirmed that mitochondrial dysfunction in the endothelial cells caused by P. gingivalis was dependent on Drp1, which may be the mechanism of P. gingivalis causing endothelial dysfunction. Nevertheless, the signalling pathway induced the mitochondrial dysfunction remains unclear. The purpose of this study was to investigate the role of the RhoA/ROCK1 pathway in regulating mitochondrial dysfunction caused by P. gingivalis. P. gingivalis was used to infect EA.hy926 cells (endothelial cells). The expression and activation of RhoA and ROCK1 were assessed by western blotting and pull‐down assay. The morphology of mitochondria was observed by mitochondrial staining and transmission electron microscopy. Mitochondrial function was measured by ATP content, mitochondrial DNA and mitochondrial permeability transition pore openness. The phosphorylation and translocation of Drp1 were evaluated using western blotting and immunofluorescence. The role of the RhoA/ROCK1 pathway in mitochondrial dysfunction was investigated using RhoA and ROCK1 inhibitors. The activation of RhoA/ROCK1 pathway and mitochondrial dysfunction were observed in P. gingivalis‐infected endothelial cells. Furthermore, RhoA or ROCK1 inhibitors partly prevented mitochondrial dysfunction caused by P. gingivalis. The increased phosphorylation and mitochondrial translocation of Drp1 induced by P. gingivalis were both blocked by RhoA and ROCK1 inhibitors. In conclusion, we demonstrate that the RhoA/ROCK1 pathway was involved in mitochondrial dysfunction caused by P. gingivalis by regulating the phosphorylation and mitochondrial translocation of Drp1. Our research illuminated a possible new mechanism by which P. gingivalis promotes endothelial dysfunction. [ABSTRACT FROM AUTHOR]

Non‐metal nitrides are an exciting field of chemistry, featuring a significant number of compounds that can possess outstanding material properties. These properties mainly rely on maximizing the number of strong covalent bonds, with crosslinked XN6 octahedra frameworks being particularly attractive. In this study, the phosphorus–nitrogen system was studied up to 137 GPa in laser‐heated diamond anvil cells, and three previously unobserved phases were synthesized and characterized by single‐crystal X‐ray diffraction, Raman spectroscopy measurements and density functional theory calculations. δ‐P3N5 and PN2 were found to form at 72 and 134 GPa, respectively, and both feature dense 3D networks of the so far elusive PN6 units. The two compounds are ultra‐incompressible, having a bulk modulus of K0=322 GPa for δ‐P3N5 and 339 GPa for PN2. Upon decompression below 7 GPa, δ‐P3N5 undergoes a transformation into a novel α′‐P3N5 solid, stable at ambient conditions, that has a unique structure type based on PN4 tetrahedra. The formation of α′‐P3N5 underlines that a phase space otherwise inaccessible can be explored through materials formed under high pressure. [ABSTRACT FROM AUTHOR]

Protein engineering through directed evolution is an effective way to obtain proteins with novel functions with the potential applications as tools for diagnosis or therapeutics. Many natural proteins have undergone directed evolution in vitro in the test tubes in the laboratories worldwide, resulting in the numerous protein variants with novel or enhanced functions. we constructed here an SH2 variant library by randomizing 8 variable residues in its phosphotyrosine (pTyr) binding pocket. Selection of this library by a pTyr peptide led to the identification of SH2 variants with enhanced affinities measured by EC50. Fluorescent polarization was then applied to quantify the binding affinities of the newly identified SH2 variants. As a result, three SH2 variants, named V3, V13 and V24, have comparable binding affinities with the previously identified SH2 triple‐mutant superbinder. Biolayer Interferometry assay was employed to disclose the kinetics of the binding of these SH2 superbinders to the phosphotyrosine peptide. The results indicated that all the SH2 superbinders have two‐orders increase of the dissociation rate when binding the pTyr peptide while there was no significant change in their associate rates. Intriguingly, though binding the pTyr peptide with comparable affinity with other SH2 superbinders, the V3 does not bind to the sTyr peptide. However, variant V13 and V24 have cross‐reactivity with both pTyr and sTyr peptides. The newly identified superbinders could be utilized as tools for the identification of pTyr‐containing proteins from tissues under different physiological or pathophysiological conditions and may have the potential in the therapeutics. [ABSTRACT FROM AUTHOR]

This letter proposes a fully domain‐independent WiFi‐based gesture recognition system based on the multi‐label adversarial network. Unlike pioneer machine learning works, our system does not require retraining in the target domain, which benefits from our key idea of eliminating fully domain information such as orientations, locations, environment information. The system proposed by us includes three parts: Feature extractor, domain discriminator, and gesture recogniser. The feature extractor attempts to deceive the domain discriminator based on the adversarial network structure so that it is difficult to judge the input domain label, thereby obtaining domain‐independent features and realising fully domain‐independent gesture recognition. Extensive experiments are conducted on the Widar 3.0 dataset and our dataset to evaluate system performance. The results show that our system can achieve an in‐domain recognition accuracy of 93.2% and a cross‐domain recognition accuracy of 87.1%, which is superior to other state‐of‐the‐art works. [ABSTRACT FROM AUTHOR]

Invited for the cover of this issue are Dominique Laniel (University of Edinburgh), Florian Trybel (University of Linköping), and their colleagues. The image depicts a bridge built of the newly discovered δ‐P3N5 solid with the structure featuring PN6 units, a previously missing connection between the carbon group elements nitrides and chalcogens nitrides. Read the full text of the article at 10.1002/chem.202201998. [ABSTRACT FROM AUTHOR]

Now, the discovery of the -P SB 3 sb N SB 5 sb and PN SB 2 sb phosphorus nitrides - formed under high pressure and both composed of the elusive PN SB 6 sb octahedron - builds a long-sought-after bridge between these two groups of nitrides. Keywords: high-pressure high-temperature synthesis; non-metal nitrides; PN6 octahedra; synchrotron single-crystal X-ray diffraction; ultra-incompressibility EN high-pressure high-temperature synthesis non-metal nitrides PN6 octahedra synchrotron single-crystal X-ray diffraction ultra-incompressibility 1 1 1 11/10/22 20221107 NES 221107 B For the last 30 years b , the lack of a binary phosphorus nitride containing PN SB 6 sb octahedra formed a scientific chasm between carbon-group and oxygen-group nitrides, both featuring a variety of solids with XN SB 6 sb units (X being a non-metal element). High-pressure high-temperature synthesis, non-metal nitrides, PN6 octahedra, synchrotron single-crystal X-ray diffraction, ultra-incompressibility. [Extracted from the article]

Transition metal nitrides, particularly those of 5d metals, are known for their outstanding properties, often relevant for industrial applications. Among these metal elements, tungsten is especially attractive given its low cost. In this high‐pressure investigation of the W–N system, two novel ultra‐incompressible tungsten nitride superconductors, namely W2N3 and W3N5, are successfully synthesized at 35 and 56 GPa, respectively, through a direct reaction between N2 and W in laser‐heated diamond anvil cells. Their crystal structure is determined using synchrotron single‐crystal X‐ray diffraction. While the W2N3 solid's sole constituting nitrogen species are N3‐ units, W3N5 features both discrete N3‐ as well as N24‐ pernitride anions. The bulk modulus of W2N3 and W3N5 is experimentally determined to be 380(3) and 406(7) GPa, and their ultra‐incompressible behavior is rationalized by their constituting WN7 polyhedra and their linkages. Importantly, both W2N3 and W3N5 are recoverable to ambient conditions and stable in air. Density functional theory calculations reveal W2N3 and W3N5 to have a Vickers hardness of 30 and 34 GPa, and superconducting transition temperatures at ambient pressure (50 GPa) of 11.6 K (9.8 K) and 9.4 K (7.2 K), respectively. Additionally, transport measurements performed at 50 GPa on W2N3 corroborate with the calculations. [ABSTRACT FROM AUTHOR]

Non‐metal nitrides are an exciting field of chemistry, featuring a significant number of compounds that can possess outstanding material properties. These properties mainly rely on maximizing the number of strong covalent bonds, with crosslinked XN6 octahedra frameworks being particularly attractive. In this study, the phosphorus–nitrogen system was studied up to 137 GPa in laser‐heated diamond anvil cells, and three previously unobserved phases were synthesized and characterized by single‐crystal X‐ray diffraction, Raman spectroscopy measurements and density functional theory calculations. δ‐P3N5 and PN2 were found to form at 72 and 134 GPa, respectively, and both feature dense 3D networks of the so far elusive PN6 units. The two compounds are ultra‐incompressible, having a bulk modulus of K0=322 GPa for δ‐P3N5 and 339 GPa for PN2. Upon decompression below 7 GPa, δ‐P3N5 undergoes a transformation into a novel α′‐P3N5 solid, stable at ambient conditions, that has a unique structure type based on PN4 tetrahedra. The formation of α′‐P3N5 underlines that a phase space otherwise inaccessible can be explored through materials formed under high pressure. [ABSTRACT FROM AUTHOR]

Invited for the cover of this issue are Dominique Laniel (University of Edinburgh), Florian Trybel (University of Linköping), and their colleagues. The image depicts a bridge built of the newly discovered δ‐P3N5 solid with the structure featuring PN6 units, a previously missing connection between the carbon group elements nitrides and chalcogens nitrides. Read the full text of the article at 10.1002/chem.202201998. [ABSTRACT FROM AUTHOR]

Non‐metal nitrides are an exciting field of chemistry, featuring a significant number of compounds that can possess outstanding material properties. These properties mainly rely on maximizing the number of strong covalent bonds, with crosslinked XN6 octahedra frameworks being particularly attractive. In this study, the phosphorus–nitrogen system was studied up to 137 GPa in laser‐heated diamond anvil cells, and three previously unobserved phases were synthesized and characterized by single‐crystal X‐ray diffraction, Raman spectroscopy measurements and density functional theory calculations. δ‐P3N5 and PN2 were found to form at 72 and 134 GPa, respectively, and both feature dense 3D networks of the so far elusive PN6 units. The two compounds are ultra‐incompressible, having a bulk modulus of K0=322 GPa for δ‐P3N5 and 339 GPa for PN2. Upon decompression below 7 GPa, δ‐P3N5 undergoes a transformation into a novel α′‐P3N5 solid, stable at ambient conditions, that has a unique structure type based on PN4 tetrahedra. The formation of α′‐P3N5 underlines that a phase space otherwise inaccessible can be explored through materials formed under high pressure. [ABSTRACT FROM AUTHOR]