The methyltransferase like 3 （METTL3）-containing methyltransferase complex catalyzes the N6-methyladenosine （m6A） formation, a novel epitranscriptomic marker; however, the nature of this complex ...remains largely unknown. Here we report two new components of the human m6A methyltransferase complex, Wilms＇ tumor 1-associating protein （WTAP） and methyltransferase like 14 （METTL14）. WTAP interacts with METTL3 and METTL14, and is required for their localization into nuclear speckles enriched with pre-mRNA processing factors and for catalytic ac- tivity of the m6A methyltransferase in vivo. The majority of RNAs bound by WTAP and METTL3 in vivo represent mRNAs containing the consensus m6A motif. In the absence of WTAP, the RNA-binding capability of METTL3 is strongly reduced, suggesting that WTAP may function to regulate recruitment of the m6A methyltransferase complex to mRNA targets. Furthermore, transcriptomic analyses in combination with photoactivatable-ribonucleoside-en- hanced crosslinking and immunoprecipitation （PAR-CLIP） illustrate that WTAP and METTL3 regulate expression and alternative splicing of genes involved in transcription and RNA processing. Morpholino-mediated knockdown targeting WTAP and/or METTL3 in zebrafish embryos caused tissue differentiation defects and increased apoptosis. These findings provide strong evidence that WTAP may function as a regulatory subunit in the m6A methyltransferase complex and play a critical role in epitranscriptomic regulation of RNA metabolism.
A convenient and rapid detection method for methanol in ethanol remains a major challenge due to their indistinguishable physical properties. Herein, a novel fluorescence probe based on perovskite ...was successfully designed to overcome this bottleneck. We report a new zero‐dimensional (0D) hybrid perovskite of MP2InxSb1−xCl7 ⋅ 6 H2O (MP=2‐methylpiperazine) displaying an unusual green light emission with near‐unity photoluminescence quantum yield. Remarkably, this 0D perovskite exhibits reversible methanol‐response luminescence switching between green and yellow color but fail in any other organic vapors. Even for blended alcohol solutions, the luminescent probe exhibits excellent sensing performance with multiple superiorities of rapid response time (30 s) and ultra‐low detection limit (40 ppm), etc. Therefore, this 0D perovskite can be utilized as a perfect fluorescence probe to detect traces of methanol from ethanol with ultrahigh sensitivity, selectivity and repeatability. To the best of our knowledge, this work represents the first perovskite as fluorescence probe for methanol with wide potential in environmental monitoring and methanol detection, etc.
0D hybrid lead‐free halide displays highly efficient broadband green light emission with a near‐unity photoluminescence quantum yield, and acts as a unique fluorescence sensor for methanol in ethanol with ultrahigh selectivity, sensitivity and repeatability as well as fast response time.
Discovery of earth-abundant electrocatalysts to replace iridium for the oxygen evolution reaction (OER) in a proton exchange membrane water electrolyzer (PEMWE) represents a critical step in reducing ...the cost for green hydrogen production. We report a nanofibrous cobalt spinel catalyst codoped with lanthanum (La) and manganese (Mn) prepared from a zeolitic imidazolate framework embedded in electrospun polymer fiber. The catalyst demonstrated a low overpotential of 353 millivolts at 10 milliamperes per square centimeter and a low degradation for OER over 360 hours in acidic electrolyte. A PEMWE containing this catalyst at the anode demonstrated a current density of 2000 milliamperes per square centimeter at 2.47 volts (Nafion 115 membrane) or 4000 milliamperes per square centimeter at 3.00 volts (Nafion 212 membrane) and low degradation in an accelerated stress test.
Epithelial cell adhesion molecule (EpCAM) is known to be highly expressed in a variety of epithelial carcinomas, and it is involved in cell adhesion and proliferation. However, its expression profile ...and biological function in nasopharyngeal carcinoma (NPC) remains unclear. In this study, higher expression of EpCAM was found in NPC samples compared with non-cancer nasopharyngeal mucosa by qRT-PCR. Additionally, immunohistochemistry (IHC) analysis of NPC specimens from 64 cases showed that high EpCAM expression was associated with metastasis and shorter survival. Multivariate survival analysis identified high EpCAM expression as an independent prognostic factor. Ectopic EpCAM expression in NPC cells promoted epithelial-mesenchymal transition (EMT), induced a cancer stem cell (CSC)-like phenotype, and enhanced metastasis in vitro and in vivo without an effect on cell proliferation. Notably, EpCAM overexpression reduced PTEN expression and increased the level of AKT, mTOR, p70S6K and 4EBP1 phosphorylation. Correspondingly, an AKT inhibitor and rapamycin blocked the effect of EpCAM on NPC cell invasion and stem-like phenotypes, and siRNA targeting PTEN rescued the oncogenic activities in EpCAM knockdown NPC cells. Our data demonstrate that EpCAM regulates EMT, stemness and metastasis of NPC cells via the PTEN/AKT/mTOR pathway.
Polymer electrolytes for lithium polymer batteries Long, Lizhen; Wang, Shuanjin; Xiao, Min ...
Journal of materials chemistry. A, Materials for energy and sustainability,
01/2016, Letnik:
4, Številka:
26
Journal Article
Recenzirano
In this review, state-of-the-art polymer electrolytes are discussed with respect to their electrochemical and physical properties for their application in lithium polymer batteries. We divide polymer ...electrolytes into the two large categories of solid polymer electrolytes and gel polymer electrolytes (GPE). The performance requirements and ion transfer mechanisms of polymer electrolytes are presented at first. Then, solid polymer electrolyte systems, including dry solid polymer electrolytes, polymer-in-salt systems (rubbery electrolytes), and single-ion conducting polymer electrolytes, are described systematically. Solid polymer electrolytes still suffer from poor ionic conductivity, which is lower than 10
−5
S cm
−1
. In order to further improve the ionic conductivity, numerous new types of lithium salt have been studied and inorganic fillers have been incorporated into solid polymer electrolytes. In the section on gel polymer electrolytes, the types of plasticizer and preparation methods of GPEs are summarized. Although the ionic conductivity of GPEs can reach 10
−3
S cm
−1
, their low mechanical strength and poor interfacial properties are obstacles to their practical application. Significant attention is paid to the incorporation of inorganic fillers into GPEs to improve their mechanical strength as well as their transport properties and electrochemical properties.
In this review, state-of-the-art polymer electrolytes are discussed with respect to their electrochemical and physical properties for their application in lithium polymer batteries.
Upon heating, polyesters decompose to small molecules and release flammable volatiles and toxic gases, primarily through chain scission of their ester linkages, and therefore exhibit poor fire‐safety ...properties, thus restricting their applications. Reported herein is an end‐group‐capturing effect of (bis)oxazoline groups, generated from the thermal rearrangement of the N‐(2‐hydroxyphenyl)phthalimide (HPI) moiety which was incorporated into the polyester chain by copolymerization. These copolyesters, as a result, exhibit high efficiency in retarding decomposition by capturing the decomposed products, particularly for the carbonyl‐terminated fragments, thus increasing the fire‐safety properties, such as self‐extinguishing, anti‐dripping, and inhibiting heat release and smoke production. The successful application of this method in both semi‐aromatic and aliphatic polyesters provide promising perspectives to designing versatile fire‐safe polymers.
Captured: End‐group capture of benzoxazole from the thermal rearrangement of a hydroxy‐containing phthalimide group contributes to the fire‐safety features of polyesters. This novel strategy exhibits applicability and efficiency for both semi‐aromatic and aliphatic polyesters, providing a new design approach to fire‐safe polymers.
To address the safety concern for room‐temperature sodium‐sulfur batteries, such as fires easily triggered by organic electrolytes, an applicable non‐flammable electrolyte formula was developed by ...introducing trimethyl phosphate (TMP) into 1.0 M NaClO4‐ethylene carbonate/propylene carbonate electrolyte. It is demonstrated that the electrolyte containing 15 wt.% TMP was a optimized formula, exhibiting nonflammability, thermal stability, electrochemical compatibility and lasting cell performance. Using this optimized electrolyte formula, the sulfur cathode exhibited a stable capacity of 788 mAh g−1 at a rate of 0.1 C and excellent rate capability of 441 and 177 mAh g−1 for 200 cycles at rates of 1 C and 5 C, respectively. When the TMP content further increases to 25 wt.%, the specific capacity of batteries declined significantly due to unstable SEI. Our study can shed light on the development of flame‐retardant electrolyte for room‐temperature sodium‐sulfur or other batteries.
Try to set the night on fire: a nonflammable electrolyte for room‐temperature sodium‐sulfur (RT Na‐S) batteries is prepared by introducing trimethyl phosphate (TMP) into 1.0 M NaClO4‐ethylene carbonate/ propylene carbonate (EC/PC) electrolyte. With 15 wt.% TMP‐contained electrolyte the C/S electrode shows excellent cycling stability with a reversible capacity of 788 mAh g−1 after 80 cycles as well as a good rate performance.
Understanding the dynamics and underlying mechanism of carbon exchange between terrestrial ecosystems and the atmosphere is one of the key issues in global change research. In this study, we ...quantified the carbon fluxes in different terrestrial ecosystems in China, and analyzed their spatial variation and environmental drivers based on the long‐term observation data of ChinaFLUX sites and the published data from other flux sites in China. The results indicate that gross ecosystem productivity (GEP), ecosystem respiration (ER), and net ecosystem productivity (NEP) of terrestrial ecosystems in China showed a significantly latitudinal pattern, declining linearly with the increase of latitude. However, GEP, ER, and NEP did not present a clear longitudinal pattern. The carbon sink functional areas of terrestrial ecosystems in China were mainly located in the subtropical and temperate forests, coastal wetlands in eastern China, the temperate meadow steppe in the northeast China, and the alpine meadow in eastern edge of Qinghai‐Tibetan Plateau. The forest ecosystems had stronger carbon sink than grassland ecosystems. The spatial patterns of GEP and ER in China were mainly determined by mean annual precipitation (MAP) and mean annual temperature (MAT), whereas the spatial variation in NEP was largely explained by MAT. The combined effects of MAT and MAP explained 79%, 62%, and 66% of the spatial variations in GEP, ER, and NEP, respectively. The GEP, ER, and NEP in different ecosystems in China exhibited ‘positive coupling correlation’ in their spatial patterns. Both ER and NEP were significantly correlated with GEP, with 68% of the per‐unit GEP contributed to ER and 29% to NEP. MAT and MAP affected the spatial patterns of ER and NEP mainly by their direct effects on the spatial pattern of GEP.
Bulk-heterojunction organic photovoltaic devices with nonfullerene acceptors (NFAs) exhibit efficient hole transfer with small interfacial energy offset, which results in power conversion ...efficiencies above 17% in single junction devices using the high-performance NFA of Y6. However, the underlying mechanism responsible for the hole transfer channel in the polymer/Y6 blends remains poorly understood. Herein, we report that the hole transfer channel of photocharge generation is mediated by an intra-moiety excited state in a blend of donor polymer PM6 and NFA Y6 using broadband transient absorption (TA) spectroscopy. By comparing the TA data recorded from the solution and film Y6 samples, we identify the ultrafast formation of an intra-moiety excimer state together with the conversion from the primary local excitation on a time scale of ∼0.2 ps in the Y6 film. The intra-moiety excimer state acts as the intermediate for the hole transfer channel, which dissociates into free polarons on a time scale of ∼15 ps in the PM6/Y6 blend at room temperature. The intra-moiety intermediate state, arising from the intermolecular coupling in Y6 domains, is markedly different from the interfacial charge transfer state, which is commonly accepted as the intermediate state for the electron transfer channel. These findings suggest that manipulating the interplay between intra-moiety and interfacial excited species can provide a promising route for further improving device performance.
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