Tunable Atomically Wide Electrostatic Barriers Embedded in a Graphene WSe2 Heterostructure

Inducing and controlling electrostatic barriers in two-dimensional (2D) quantum materials has shown extraordinary promise to enable control of charge carriers, and is key for the realization of nanoscale electronic and optoelectronic devices1-10. Because of their atomically thin nature, the 2D materials have a congenital advantage to construct the thinnest possible p-n junctions1,3,7,9,10. To realize the ultimate functional unit for future nanoscale devices, creating atomically wide electrostatic barriers embedded in 2D materials is desired and remains an extremely challenge. Here we report the creation and manipulation of atomically wide electrostatic barriers embedded in graphene WSe2 heterostructures. By using a STM tip, we demonstrate the ability to generate a one-dimensional (1D) atomically wide boundary between 1T-WSe2 domains and continuously tune positions of the boundary because of ferroelasticity of the 1T-WSe2. Our experiment indicates that the 1D boundary introduces atomically wide electrostatic barriers in graphene above it. Then the 1D electrostatic barrier changes a single graphene WSe2 heterostructure quantum dot from a relativistic artificial atom to a relativistic artificial molecule

γ-Tocotrienol Induces Paraptosis-Like Cell Death in Human Colon Carcinoma SW620 Cells

Colorectal cancer is one of the most serious illnesses among diagnosed cancer. As a new type of anti-cancer composition from tocotrienol-rich fraction of palm oil, γ-tocotrienol is widely used in anti-cancer research. The objectives of this study were to investigate the effects of γ-tocotrienol on human colon cancer SW620 and HCT-8 cells. We showed that treatment with different concentrations of γ-tocotrienol resulted in a dose dependent inhibition of cell growth. Cell death induced by γ-tocotrienol was mediated by a paraptosis-like cell death in SW620 and HCT-8 cells. Real-time RT-PCR and western blot analyses showed that γ-tocotrienol inhibited the expression level of β-catenin, cyclin D1 and c-jun. These data suggest that a paraptosis-like cell death induced by γ-tocotrienol in SW620 cells is associated with the suppression of the Wnt signaling pathway, which offers a novel tool for treating apoptosis-resistance colon cancer

High optical transmittance of aluminum ultrathin film with hexagonal nanohole arrays as transparent electrode

We fabricate samples of aluminum ultrathin films with hexagonal nanohole arrays and characterize the transmission performance. High optical transmittance larger than 60% over a broad wavelength range from 430 nm to 750 nm is attained experimentally. The Fano-type resonance of the excited surface plasmon plaritons and the directly transmitted light attribute to both of the broadband transmission enhancement and the transmission suppression dips

A wear-resistant metastable CoCrNiCu high-entropy alloy with modulated surface and subsurface structures

Sliding friction-induced subsurface structures and severe surface oxidation can be the major causes influencing the wear resistance of ductile metallic materials. Here, we demonstrated the role of subsurface and surface structures in enhancing the wear resistance of an equiatomic metastable CoCrNiCu high-entropy alloy (HEA). The CoCrNiCu HEA is composed of a CoCrNi-rich face-centered cubic (FCC) dendrite phase and a Cu-rich FCC inter-dendrite phase. Copious Cu-rich nano-precipitates are formed and distributed uniformly inside the dendrites after tuning the distribution and composition of the two phases by thermal annealing. Although the formation of nano-precipitates decreases the hardness of the alloy due to the loss of solid solution strengthening, these nano-precipitates can be deformed to form continuous Cu-rich nanolayers during dry sliding, leading to a self-organized nano-laminated microstructure and extensive hardening in the subsurface. In addition, the nano-precipitates can facilitate the formation of continuous and compacted glaze layers on the worn surface, which are also beneficial for the reduction of the wear rate of CoCrNiCu. The current work can be extended to other alloy systems and might provide guidelines for designing and fabricating wear-resistant alloys in general

Gallic acid pyridine monosolvate

In the title compound (systenatic name: 3,4,5-trihy­droxy­benzoic acid pyridine monosolvate), C5H5N·C7H6O5, the gallic acid mol­ecule is essentially planar (r.m.s deviation = 0.0766 Å for non-H atoms) and is linked to the pyridine mol­ecule by an O—H⋯N hydrogen bond. An intra­molecular O—H⋯O hydrogen bond occurs in the gallic acid mol­ecule. The gallic acid and pyridine mean planes make a dihedral angle 12.6 (3)°. Inter­molecular O—H⋯O and O—H⋯N hydrogen bonding involving the hy­droxy and carboxyl groups and the pyridine mol­ecule, and π–π inter­actions between inversion-related pyridines [centroid–centroid distance = 3.459 (6) Å] and between pyridine and benzene rings [centroid–centroid distance = 3.548 (6) Å], lead to a three-dimensional network in the crystal

Genomic diversity among Basmati rice (Oryza sativa L) mutants obtained through 60Co gamma radiations using AFLP markers

Mutation breeding can be considered successful in obtaining new cultivars and broadening the genetic base of rice crop. In order to obtain new varieties of rice with improved agronomic and grain characteristics, gamma radiation (60Co) has been used to generate novel mutants of the Basmati rice. In this study rice cultivars; Basmati-370 and Basmati-Pak, were exposed to different doses of gamma radiations and stable mutants along with parents were studied for genomic diversity on the basis of molecular marker (AFLP). Morphological data showed that mutants of Basmati-370 performed well for yield and yield components and grain physical parameters whereas, the mutant EL-30-2-1 has extra long rain trait as compared to the parent (Basmati-Pak). The genetic variations determined through AFLP revealed a total of 282 scorable bands, out of which 108 (37.81%) were polymorphic. The number of fragments produced by various primers combinations ranged from 11 - 26 with an average of 17.63fragments per primer combination. Maximum 26 bands were amplified with P-AAG/M-CAG primer combination and minimum one band was amplified with P-ATG/M-CTA primer combination. Two groups of genotypes were detected; group-A had DM-1-30-3-99, DM-1-30-34-99 and EF-1-20-52-04 mutants along with parent Basmati-370, whereas the group-B contained EL-30-2-1 and parent Basmati-Pak. The results of AFLP analysis indicated that the rate of polymorphism was 4.43% (DM-1-30-3-99), 4.25% (DM-1-30-34-99) and 6.38% (EF-1-20-52-04) among the genomes of mutants and parent Basmati-370, respectively, whereas polymorphism rate was 5.32% between genome of EL-30-2-1 and Basmati-Pak. The study further confirmed that the use of gamma radiations is an effective approach for creating new rice germplasm

Sodium-glucose cotransporter 2 inhibitors (SGLT2i) and cardiac arrhythmias:a systematic review and meta-analysis

Following publication of the original article [1], the authors noticed an error in the second author’s name. The name of the second author, "Gregory Y. H. Lip", was incorrectly written as "Gregory-Y H Lip". This has been corrected with this erratum. The original article [1] has been corrected

Bioactivities of berberine metabolites after transformation through CYP450 isoenzymes

<p>Abstract</p> <p>Background</p> <p>Berberine (BBR) is a drug with multiple effects on cellular energy metabolism. The present study explored answers to the question of which CYP450 (Cytochrome P450) isoenzymes execute the phase-I transformation for BBR, and what are the bioactivities of its metabolites on energy pathways.</p> <p>Methods</p> <p>BBR metabolites were detected using LC-MS/MS. Computer-assistant docking technology as well as bioassays with recombinant CYP450s were employed to identify CYP450 isoenzymes responsible for BBR phase-I transformation. Bioactivities of BBR metabolites in liver cells were examined with real time RT-PCR and kinase phosphorylation assay.</p> <p>Results</p> <p>In rat experiments, 4 major metabolites of BBR, berberrubine (M1), thalifendine (M2), demethyleneberberine (M3) and jatrorrhizine (M4) were identified in rat's livers using LC-MS/MS (liquid chromatography-tandem mass spectrometry). In the cell-free transformation reactions, M2 and M3 were detectable after incubating BBR with rCYP450s or human liver microsomes; however, M1 and M4 were below detective level. CYP2D6 and CYP1A2 played a major role in transforming BBR into M2; CYP2D6, CYP1A2 and CYP3A4 were for M3 production. The hepatocyte culture showed that BBR was active in enhancing the expression of insulin receptor (InsR) and low-density-lipoprotein receptor (LDLR) mRNA, as well as in activating AMP-activated protein kinase (AMPK). BBR's metabolites, M1-M4, remained to be active in up-regulating InsR expression with a potency reduced by 50-70%; LDLR mRNA was increased only by M1 or M2 (but not M3 and M4) with an activity level 35% or 26% of that of BBR, respectively. Similarly, AMPK-α phosphorylation was enhanced by M1 and M2 only, with a degree less than that of BBR.</p> <p>Conclusions</p> <p>Four major BBR metabolites (M1-M4) were identified after phase-I transformation in rat liver. Cell-free reactions showed that CYP2D6, CYP1A2 and CYP3A4 seemed to be the dominant CYP450 isoenzymes transforming BBR into its metabolites M2 and M3. BBR's metabolites remained to be active on BBR's targets (InsR, LDLR, and AMPK) but with reduced potency.</p