Protein Interactome Analysis of the Type IX Secretion System Identifies PorW as the Missing Link between the PorK/N Ring Complex and the Sov Translocon

The T9SS is a newly identified protein secretion system of the Fibrobacteres - Chlorobi - Bacteroidetes superphylum used by pathogens associated with diseases of humans, fish, and poultry for the secretion and cell surface attachment of virulence factors. The T9SS comprises three known modules: (i) the trans-envelope core module comprising the PorL/M motor and the PorK/N ring, (ii) the outer membrane Sov translocon, and (iii) the cell surface attachment complex.

Permian Ages of “Younger Granites” from Mounio Province (Gouré area, Southeastern Niger)

African formations intruded by the “Younger Granites” ring complex. In the study area, the “Younger Granites” are represented by volcanic to acid plutonic rocks with hyperalkaline trends (pyroclastic rocks, rhyolites, microgranites, granites, syenites), forming in the North, a circular structure called Gouré ring complex. Preliminary geochronological datings of the Mounio granites have yielded Carboniferous ages. However, recent investigations carried out in this province have identified structures similar to Pan-African deformation structures, such as folds and several generations of schistosity/foliation. Analysis of the relationship between deformation and magmatism has removed any ambiguity regarding the relative age of the deformation. This study focuses on the radiometric dating of the “Younger Granites” of Gouré area, in order to update the geochronological data. Thus, three samples (pyroclastitic rock, rhyolite, microgranite) were dated by the K-Ar method on total rock using a mass spectrometertype MI 1201 IG. Radiometric dating results assign a Lower Permian age (293-287 Ma) to the “Younger Granites” Ring Complex of the Mounio Province in Niger, classically considered to be Carboniferous in age.

Dysregulation of Microtubule Nucleating Proteins in Cancer Cells

In cells, microtubules typically nucleate from microtubule organizing centers, such as centrosomes. γ-Tubulin, which forms multiprotein complexes, is essential for nucleation. The γ-tubulin ring complex (γ-TuRC) is an efficient microtubule nucleator that requires additional centrosomal proteins for its activation and targeting. Evidence suggests that there is a dysfunction of centrosomal microtubule nucleation in cancer cells. Despite decades of molecular analysis of γ-TuRC and its interacting factors, the mechanisms of microtubule nucleation in normal and cancer cells remains obscure. Here, we review recent work on the high-resolution structure of γ-TuRC, which brings new insight into the mechanism of microtubule nucleation. We discuss the effects of γ-TuRC protein dysregulation on cancer cell behavior and new compounds targeting γ-tubulin. Drugs inhibiting γ-TuRC functions could represent an alternative to microtubule targeting agents in cancer chemotherapy.

Mineralogical Criteria for Genetic Relationship of Igneous and Carbonatite Rocks of the Tomtor Massif (Siberian Platform)

The Tomtor massif, located in the north-east of the Siberian Platform, is a polychronous zonal-ring complex of alkaline ultrabasic rocks and carbonatites containing a unique deposit of Nb and REE. A comparative analysis of the typomorphic features of minerals of different types of silicate rocks and carbonatites of the Tomtor massif is given in order to establish their convergent features. In order to exclude the mutual influence of rocks formed at different times on each other, samples were taken from different dispersed independent pipe-like bodies of melteigites, a sheet body of alkaline picrites and a transverse dike of carbonatite located south of the Tomtor massif, as well as from alkaline syenites from the southern margin of the massif. It is shown that interesting convergent features are identified in the rock-forming and accessory minerals, including rare-metal ore minerals of different silicate igneous rocks and carbonatite formations. Rock-forming minerals - pyroxenes, micas, feldspars, feldspathopids, garnets, as well as basic and rare carbonates, oxide ore minerals, including Cr-containing spinelides, and sulfide and other exotic phases have such features. The confirmation of the convergence of a group of obvious high-temperature early magmatic elements-MgO, Cr, and Ni - with a group of CaO, CO2, H2O, P2O5, and Y components forming carbonatite derivatives was the most interesting nuance in this regard. Existence of such polychromous complicated ore-magmatic ring complexes as Tomtor massif indicates occurrence of intraplate deep large magma-generating hearths in lithosphere mantle. Such easily fusible hearths, conserved in lithosphere mantle of residual melts of kimberlite, alkali-picrites, carbonatite compositions, under the subsequent favorable geodynamic settings, are subject to rapid flotation, undergoing decompression melting and forming concentric-zonal platform complexes of alkali ultrabasic rocks with carbonatites

Sutureless “Contact Lens Sandwich” Technique for Amniotic Membrane Therapy of Central Corneal Ulcers

Purpose To describe a new technique for sutureless and glue-free amniotic membrane transplantation (AMT) and to investigate its effectiveness to treat corneal persistent epithelial defects (PEDs), compared to bandage contact lens (BCL) application alone. Methods We performed AMT with “contact lens sandwich technique” (CLS-AMT) in 8 consecutive patients with central/para-central (up to 4.00 mm from the geometrical centre) PED/ulceration and we retrospectively compared the results with 11 BCL procedures. Results The procedures were performed successfully with no complications. CLS-AMT showed significantly shorter healing time than BCL (24.0 ± 19.1 vs 42.9 ± 14.6 days; P < 0.05, Mann-Whitney test). Recurrence rates were 12% and 27% for CLS-AMT and BCL, respectively. Conclusion CLS-AMT technique, based on the suction effect due to the superposition of a bandage contact lens on the AM-ring complex, represents a quick, low cost, easy to perform and nearly non-invasive AMT technique. This approach is able to provide adequate fixation of AM, and it seems to be a safe and effective treatment for patients with PEDs.

Exploring the Expression and Prognostic Value of the TCP1 Ring Complex in Hepatocellular Carcinoma and Overexpressing Its Subunit 5 Promotes HCC Tumorigenesis

T-complex protein-1 ring complex (TRiC), also known as Chaperonin Containing T-complex protein-1 (CCT), is a multisubunit chaperonin required for the folding of nascent proteins. Mounting evidence suggests that TRiC also contributes to the development and progression of tumors, but there are limited studies on pathogenic functions in hepatocellular carcinoma (HCC). We comprehensively evaluated the expression pattern and biological functions of TRiC subunits using The Cancer Genome Atlas and The Human Protein Atlas. Expression levels of TRiC subunits TCP1, CCT2/3/4/5/6A/7/8 were significantly upregulated in HCC tissues at both transcript and protein levels, which predicted shorter overall survival (OS). Moreover, high mutation rates were found in several CCT subunits, and patients with altered CCT genes exhibited poorer clinical outcomes. Functional enrichment analysis showed that co-regulated genes were preferentially involved in ‘protein folding’ and ‘microtubule-based process’, while genes co-expressed with CCT subunits were primarily involved in ‘ribosome’ and ‘spliceosome’. Knockout of CCT5 in a HCC cell line reduced while overexpression enhanced proliferation rate, cycle transition, migration, and invasion. In conclusion, these findings suggest that subunits of the TRiC may be potential biomarkers for the diagnosis of HCC and play an important role in the occurrence and development of HCC.

Hydration dynamics gives the distinctive brown color in the "brown ring" nitrate test

The chemistry of the brown-ring test has been investigated for nearly a century. Though recent studies have focused on solid state structure determination and the measurement of spectra, mechanistic details and kinetics, the aspects of solution structure and dynamics remain unknown. From ab initio molecular dynamics simulations of the brown-ring complex in aqueous solution, we have identified that the classically established pseudo-octahedral [Fe(H2O)5(NO)]2+ complex is in equilibrium with a square-pyramidal [Fe(H2O)4(NO)]2+ complex through the exchange of one of the coordinated H2O molecules. We also find, using ab-initio multi-reference methods, that the mixture of these two complexes is what gives the distinctive brown coloration to the brown-ring test. We show that its UV-vis spectrum can be theoretically reproduced only by accounting these two species and not the [Fe(H2O)5(NO)]2+ complex alone. The energetics of the two complexes are also investigated with multi-reference methods.

Hydration dynamics gives the distinctive brown color in the "brown ring" nitrate test

The brown ring test is one of the most popular and visually appealing reagent tests, commonly known to chemistry undergrads and familiar even to school students. The exact composition, mechanism and structure of the complex has been investigated for nearly a century. Recent studies have elucidated its UV-vis, EPR and Mossbauer spectra, mechanistic details and kinetics, followed by crystallization and structure determination in solid state. Nonetheless these studies were unable to address the aspects of solution structure and dynamics of the brown ring complex. We have conducted ab initio molecular dynamics simulations of the classic brown ring complex in aqueous solution. In the process from the simulation trajectory, we have identified that the classically established pseudo-octahedral [Fe(H2O)5(NO)]2+ complex is in chemical equilibrium with the square-pyramidal [Fe(H2O)4(NO)]2+ complex through the exchange of one of the coordinated H2O molecules. The dynamics in aqueous solution between the penta-aqua and tetra-aqua complexes in the brown ring system has to our knowledge never been suggested earlier. Interestingly we find, using ab initio multi-reference quantum chemical methods i.e. CASSCF/NEVPT2 and CASPT2 calculations, that the mixture of these two complexes is what gives the distinctive brown coloration to the brown ring test. We show that its UV-vis spectrum can be theoretically reproduced only by accounting these two species, and not solely the classically established [Fe(H2O)5(NO)]2+ complex. The energetics of the penta-aqua and tetra-aqua complexes is also investigated at the level of multi-reference quantum chemical methods.

Pd Doped on TCH@SBA-15 Nanocomposites: Fabrication and Application as a New Organometallic Catalyst in the Three-Component Synthesis of N-Benzo-imidazo- or -thiazole-1,3-thiazolidinones

In this study, Pd(II)/TCH@SBA-15 nanocomposites were synthesized by the grafting of 3-chloropropyltriethoxysilane and thiocarbohydrazide on SBA-15 and subsequent deposition of palladium acetates through the ligand–metal coordination method. The structure and morphology of this nanoporous nanocomposite was thoroughly identified by Fourier transform infrared spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, thermogravimetric analysis, atomic absorption spectroscopy, and Brunauer–Emmett–Teller instrumental analyses. Furthermore, the catalytic activity of this nanocomposite was investigated in the three-component synthesis of 3-benzimidazolyl or benzothiazoleyl-1,3-thiazolidin-4-ones via a reaction of 2-aminobenzimidazole or 2-aminobenzothiazole, aromatic aldehydes, and thioglycolic acid in an acetone–H2O mixture under green conditions. The Pd/TCH@SBA-15 nanocatalyst is demonstrated to exhibit a high catalyzing activity in the three-component reaction of the synthesis of N-heterocyclic thiazolidinones with good to excellent yields. One of the advantages of the suggested method is the direct application of the thiocarbohydrazide ligand to stabilize Pd nanoparticles through formation of a stable ring complex without creating an additional Schiff base step. Moreover, this organometallic nanocatalyst can be recycled several times with no notable leaching or loss of performance.