Female frogs communicate with males through blinking.

Blinking is a behavior unique to animal taxa with motile eyelids, such as most amphibians and reptiles as well as all birds and mammals1. Eyelid movement has physiological functions, such as lubricating the cornea and washing away dust, but its potential signaling functions are not well understood1,2. The use of eyeblinks as a social signal is currently thought to be restricted to some primates, especially humans and their companion animals, but has not been verified in other taxa1,3,4. Here, through field observation and experiments, we demonstrate that female concave-eared torrent frogs (Odorrana tormota), which inhabit noisy streams, use eyeblinks to communicate with males to urge them to initiate amplexus for mating. Our findings reveal that eyeblinks may serve as a social signal in non-primate species.

Frequency jumps and subharmonic components in calls of female Odorrana tormota differentially affect the vocal behaviors of male frogs.

Studies have demonstrated that the sounds of animals from many taxa with nonlinear phenomena (NLP)-caused by nonlinear characteristics of vocal organ dynamics that lead to nonlinear vocal phenomena-can influence the behavior of receivers. However, the specific functions of different NLP components have received less attention. In most frog species, females produce few or no vocalizations; in contrast, female Odorrana tormota exhibit a diverse range of calls that are rich in NLP components. Previous field playbacks have shown that the female calls can elicit responses from male frogs. Therefore, we conducted a phonotaxis experiment to investigate the differential effects of different NLP calls by female O. tormota on the vocal behavior of male frogs. The results revealed that calls with subharmonics elicited a greater number of short calls and answering calls from male frogs compared to calls with frequency jumps. However, calls with frequency jumps triggered more staccato calls from males than calls with subharmonics. Additionally, during the phonotaxis experiments, we recorded the initial vocalizations of males in response to playbacks of female calls. The majority of males first produced short calls. Under calls with frequency jumps, most of male frogs approaching within 10 cm of the loudspeaker produced staccato calls instead of "meow" calls or short calls. While under calls with subharmonics, most male frogs preferred to produced short calls. Our findings demonstrate that frequency jumps and subharmonic components in the calls of female O. tormota have different effects on male vocal behaviors. The current study lays a foundation for a further understanding of the function of anuran NLP components.

A Non-G-Quadruplex DNA Aptamer Targeting NCL for Diagnosis and Therapy in Bladder Cancer.

Bladder cancer (BC) is a highly aggressive malignant tumor affecting the urinary system, characterized by metastasis and a poor prognosis that often leads to limited therapeutic success. This study aims to develop a novel DNA aptamer for the diagnosis and treatment of BC using a tissue-based systematic evolution of ligands by an exponential enrichment (SELEX) process. By using SELEX, this work successfully generates a new aptamer named TB-5, which demonstrates a remarkable and specific affinity for nucleolin (NCL) in BC tissues and displays marked biocompatibility both in vitro and in vivo. Additionally, this work shows that NCL is a reliable tissue-specific biomarker in BC. Moreover, according to circular dichroism spectroscopy, TB-5 forms a non-G-quadruplex structure, distinguishing it from the current NCL-targeting aptamer AS1411, and exhibits a distinct binding region on NCL compared to AS1411. Notably, this study further reveals that TB-5 activates NCL function by promoting autophagy and suppressing the migration and invasion of BC cells, which occurs by disrupting mRNA transcription processes. These findings highlight the critical role of NCL in the pathological examination of BC and warrant more comprehensive investigations on anti-NCL aptamers in BC imaging and treatment.

Targeting tumor endothelial cells with methyltransferase inhibitors: Mechanisms of action and the potential of combination therapy.

Tumor endothelial cells (TECs) reside in the inner lining of blood vessels and represent a promising target for targeted cancer therapy. DNA methylation is a chemical process that involves the transfer of a methyl group to a specific base in the DNA strand, catalyzed by a DNA methyltransferase (DNMT). DNMT inhibitors (DNMTis) can inhibit the activity of DNMTs, thereby preventing the transfer of methyl groups from s-adenosyl methionine (SAM) to cytosine. Currently, the most viable therapy for TECs is the development of DNMTis to release cancer suppressor genes from their repressed state. In this review, we first outline the characteristics of TECs and describe the development of tumor blood vessels and TECs. Abnormal DNA methylation is closely linked to tumor initiation, progression, and cell carcinogenesis, as evidenced by numerous studies. Therefore, we summarize the role of DNA methylation and DNA methyltransferase and the therapeutic potential of four types of DNMTi in targeting TECs. Finally, we discuss the accomplishments, challenges, and opportunities associated with combination therapy with DNMTis for TECs.

Female large odorous frogs (Odorrana graminea) prefer males with higher nonlinear vocal components.

In anurans, the complexity of courtship calls may affect female mate choice. The current study suggests that nonlinear phenomena (NLP) components can contribute to increasing complexity in courtship calls and attracting female attention. The results of a recent study showed that calls of large odorous frog (Odorrana graminea) contained NLP components. However, whether the nonlinear components of courtship calls in O. graminea improve male attractiveness remains unknown. We hypothesized that female O. graminea would prefer males producing calls with a higher proportion of NLP components (P-NLP-C). To test this hypothesis, we recorded the advertisement calls of 28 males and confirmed that the P-NLP-C was significantly positively related to body size. We also measured the body size of natural amplectant males and non-amplectant males in the field and found that amplectant males had larger body sizes than non-amplectant males, and the results of two-choice amplexus experiments similarly revealed a female preference for males with larger body sizes. Additionally, phonotaxis experiments also revealed that females preferred male calls with a high P-NLP-C. The results suggest that a higher P-NLP-C in calls can enhance male attractiveness, and the P-NLP-C may provide key information about male body conditions for female O. graminea. Our study provides a new insight for better understanding the role of NLP in anuran mate selection.

Aluminum-doping-based method for the improvement of the cycle life of cobalt-nickel hydroxides for nickel-zinc batteries.

The unsatisfactory cycle life of nickel-based cathodes hinders the widespread commercial usage of nickel-zinc (Ni-Zn) batteries. The most frequently used methods to improve the cycle life of Ni-based cathodes are usually complicated and/or involve using organic solvents and high energy consumption. A facile process based on the hydrolysis-induced exchange of the cobalt-based metal-organic framework (Co-MOF) was developed to prepare aluminum (Al)-doped cobalt-nickel double hydroxides (Al-CoNiDH) on a carbon cloth (CC). The entire synthesis process is highly efficient, energy-saving, and has a low negative impact on the environment. Compared to undoped cobalt-nickel double hydroxide (Al-CoNiDH-0%), the as-prepared Al-CoNiDH as the electrode material displays a remarkably improved cycling stability because the Al-doping successfully depresses the transition in the crystal phase and microstructure during the long cycling. Benefiting from the improved performance of the optimal Al-CoNiDH electrode (Al-CoNiDH-5% electrode), the as-constructed aqueous Ni-Zn battery with Al-CoNiDH-5% as the cathode (Al-CoNiDH-5%//Zn) displays more than 14% improvement in the cycle life relative to the Al-CoNiDH-0%//Zn battery. Moreover, this Al-CoNiDH-5%//Zn battery achieves a high specific capacity (264 mAh g-1), good rate capability (72.4% retention at a 30-fold higher current), high electrochemical energy conversion efficiency, superior fast-charging ability, and strong capability of reversible switching between fast charging and slow charging. Furthermore, the as-assembled quasi-solid-state Al-CoNiDH-5%//Zn battery exhibits a decent electrochemical performance and satisfactory flexibility.

Rational design of cobalt-nickel double hydroxides for flexible asymmetric supercapacitor with improved electrochemical performance.

Rational design of micro-nano morphology and suitable crystalline structure are highly desired for metal hydroxides to achieve overall high-performance in the advanced electrodes for flexible supercapacitors. Herein, a novel wisteria flower-like microstructure of cobalt-nickel double hydroxide (CoNi-DH) is successfully constructed on carbon cloth (CC) using an in-situ hydrolysis-induced exchange process between hydroxide ions and organic ligands of the Co-MOF in four different kinds of solutions containing Ni2+. The as-prepared wisteria flower-like microstructure grown on CC shows vertically aligned arrays with high specific area and abundant active sites, which not only guarantee the CoNi-DH active materials to be thoroughly exposed in the electrolyte, resulting in highly effective pseudocapacitive energy storage, but also are beneficial to rapid and reversible redox kinetics and thus give rise to high-rate capability. In addition, compared to Ni(NO3)2, NiCl2, and Ni(CH3COO)2 solutions, the Ni2SO4 solution is found to facilitate the formation of the most regular morphology and the largest interlayer spacing on (003) plane of the layered nickel hydroxide phase in the resultant CoNi-DH. As a result, the optimal CoNi-DH-S@CC (CoNi-DH prepared in Ni2SO4) serves as an advanced electrode to show high-rate capability (only 13% Cs decay after a 15-fold current elevation) and a superior specific capacity (Cs) of 929.4 C g-1, which remarkably exceeds those of CoNi-DH-N (823.1 C g-1, in Ni(NO3)2), CoNi-DH-Cl (798.4 C g-1, in NiCl2), CoNi-DH-C (803.8 C g-1, in Ni(CH3COO)2), and other similar metal hydroxides. Moreover, with this CoNi-DH-S electrode as the positive electrode, the as-prepared asymmetric supercapacitor (ASC) delivers an impressive capacity of 204.8 C g-1, a superior energy density of 42.5 Wh kg-1, and satisfactory cycle life (81.5% reservation after 7500 cycles). As a proof-of-concept application, a quasi-solid-state ASC is further successfully fabricated based on the CoNi-DH-S electrode to exhibit encouraging application potential.

Electrochemically Stable Cobalt⁻Zinc Mixed Oxide/Hydroxide Hierarchical Porous Film Electrode for High-Performance Asymmetric Supercapacitor.

Construction of electrochemically stable positive materials is still a key challenge to accomplish high rate performance and long cycling life of asymmetric supercapacitors (ASCs). Herein, a novel cobalt⁻zinc mixed oxide/hydroxide (CoZn-MOH) hierarchical porous film electrode was facilely fabricated based on a cobalt⁻zinc-based metal⁻organic framework for excellent utilization in ASC. The as-constructed hierarchical porous film supported on conductive Ni foam possesses a rough surface and abundant macropores and mesopores, which allow fast electron transport, better exposure of electrochemically active sites, and facile electrolyte access and ion diffusion. Owing to these structural merits in collaboration, the CoZn-MOH electrode prepared with a zinc feeding ratio up to 45% at 110 min of heating time (CoZn-MOH-45-110) exhibited a high specific capacitance of 380.4 F·g-1, remarkable rate capability (83.6% retention after 20-fold current increase), and outstanding cycling performances (96.5% retention after 10,000 cycles), which exceed the performances of similar active electrodes. Moreover, an ASC based on this CoZn-MOH-45-110 electrode exhibited a high specific capacitance of 158.8 F·g-1, an impressive energy density of 45.8 Wh·kg-1, superior rate capability (83.1% retention after 50-fold current increase), and satisfactory cycling stability (87.9% capacitance retention after 12,000 cycles).

Facile Activation of Commercial Carbon Felt as a Low-Cost Free-Standing Electrode for Flexible Supercapacitors.

High cost, low capacitance, and complicated synthesis process are still the key limitations for carbon-negative materials to meet their industrial production and application in high-energy-density asymmetric supercapacitors (ASCs). In this work, we demonstrate the facile preparation of ultrahigh-surface-area free-standing carbon material from low-cost industrial carbon felt (CF) and its application for flexible supercapacitor electrode with outstanding performance. Through a simple freeze-drying-assisted activation method, the as-prepared activated CF (ACF) was endowed with satisfactory flexibility, ultrahigh specific surface area of 2109 m2 g-1, good electric conductivity (311 S m-1), and excellent wettability to aqueous electrolyte. Owing to these merits, the ACF expressed an ultrahigh areal capacitance of 1441 mF cm-2, a high specific capacitance ( Cs) of 280 F g-1 based on the mass of the whole electrode, and an impressive cycling stability (87% retention after 5000 cycles). When applied as a flexible freestanding electrode for MnO2//ACF ASCs, the ACF-based device provided satisfactory areal energy densities of 0.283 and 0.104 mWh cm-2 in aqueous and quasi-solid electrolytes, respectively. The values outperform many previously reported carbon-based electrochemical devices. The low cost of raw material and the facile fabrication process, together with the high electrochemical performance, make our ACF electrode highly applicable for the mass production of flexible energy-storage devices.

Energy-Saving Synthesis of MOF-Derived Hierarchical and Hollow Co(VO3)2-Co(OH)2 Composite Leaf Arrays for Supercapacitor Electrode Materials.

A one-step and energy-saving method was proposed to synthesize hierarchical and hollow Co(VO3)2-Co(OH)2 composite leaf arrays on carbon cloth, which expressed high capacitance (522 mF cm-2 or 803 F g-1 at the current density of 0.5 mA cm-2), good rate capability (79.5% capacitance retention after a 30-fold increase of the current density) and excellent cycling stability (90% capacitance retention after 15 000 charge-discharge cycles) when tested as a supercapacitor electrode.

Crystal Structure of the Isocitrate Dehydrogenase 2 from Acinetobacter baumannii (AbIDH2) Reveals a Novel Dimeric Structure with Two Monomeric-IDH-Like Subunits.

Monomeric isocitrate dehydrogenases (IDHs) have a single polypeptide sizing around 85 kDa. The IDH2 from the opportunistic bacterium Acinetobacter baumannii (AbIDH2) with a mass of 83 kDa was formerly recognized as a typical monomeric IDH. However, both size exclusion chromatography and analytical ultracentrifugation analysis indicated that AbIDH2 exists as a homodimer in solution. The crystallographic study of the substrate/coenzyme-free AbIDH2 gave a dimeric structure and each subunit contained a domain I and a domain II. The dimeric assembly is mainly stabilized by hydrophobic interactions (16 hydrogen bonds and 11 salt bridges) from the dimer's interface platform, which centered around the three parallel helices (α4, α12, and α17) and one loop from the domain II. Kinetic analysis showed that the dimeric AbIDH2 showed much lower catalytic efficiency (0.39 µM-1·s-1) as compared to the typical monomeric IDHs (~15 µM-1·s-1). Key residues crucial for dimer formation were simultaneously changed to generate the mutant mAbIDH2. The disruption of the hydrophobic forces disassociated the dimeric AbIDH2, making mAbIDH2 a monomeric enzyme. mAbIDH2 sustained specific activity (21.9 ± 2 U/mg) comparable to AbIDH2 (25.4 ± 0.7 U/mg). However, mAbIDH2 proved to be a thermolabile enzyme, indicating that the thermostable dimeric AbIDH2 may have a physiological significance for the growth and pathogenesis of A. baumannii. Phylogenetic analysis demonstrated the existence of numerous AbIDH2 homologous proteins, thus expanding the monomeric IDH protein family.

Synthesis of NiMn-LDH Nanosheet@Ni3S2 Nanorod Hybrid Structures for Supercapacitor Electrode Materials with Ultrahigh Specific Capacitance.

One of the key challenges for pseudocapacitive electrode materials with highly effective capacitance output and future practical applications is how to rationally construct hierarchical and ordered hybrid nanoarchitecture through the simple process. Herein, we design and synthesize a novel NiMn-layered double hydroxide nanosheet@Ni3S2 nanorod hybrid array supported on porous nickel foam via a one-pot hydrothermal method. Benefited from the ultrathin and rough nature, the well-defined porous structure of the hybrid array, as well as the synergetic effect between NiMn-layered double hydroxide nanosheets and Ni3S2 nanorods, the as-fabricated hybrid array-based electrode exhibits an ultrahigh specific capacitance of 2703 F g-1 at 3 A g-1. Moreover, the asymmetric supercapacitor with this hybrid array as a positive electrode and wood-derived activated carbon as a negative electrode demonstrates high energy density (57 Wh Kg-1 at 738 W Kg-1) and very good electrochemical cycling stability.

Point mutation (R153H or R153C) in Escherichia coli isocitrate dehydrogenase: Biochemical characterization and functional implication.

Arginine 132 (R132) mutations to histidine or cysteine frequently occur to cytosolic NADP+ -isocitrate dehydrogenase (IDH1) in secondary glioblastoma multiforme (GBM) patients, in which GBM develops from a lower grade astroctyoma. Mutant enzymes lose the normal IDH activity, but acquire a neomorphic ability of producing 2-hydroxyglutarate (2-HG) from α-ketoglutarate (α-KG). In the present study, the analogous mutations, Arg to His or Cys, were employed to homologous Arg153 of the NADP+ -IDH from Escherichia coli (EcIDH), generating two mutants: EcIDH R153 H and EcIDH R153C. The mutations dramatically reduced the catalytic efficiencies (kcat /Km ) of EcIDH R153H and EcIDH R153C for isocitrate oxidation, which dropped to only 0.6 and 1.5% of the wild-type enzyme, respectively. Neoenzymatic activities of catalyzing α-KG to 2-HG by EcIDH R153H and EcIDH R153C were confirmed by GC/TOF-MS analysis. The Km values of EcIDH R153H and EcIDH R153C displayed for α-KG were 3.3 ± 0.12 and 2.2 ± 0.13 mM, respectively, and the catalytic efficiencies (kcat /Km ) of the two mutants for α-KG were 300 and 450 M-1 s-1 , respectively. As human IDH1 Arg132 mutation is cancer-associated, the present study provides new information for the in-depth investigation of the metabolic influence of EcIDH Arg mutation in vivo.

[Concentrations and health risks of toxic metals in surface dust in kindergartens of Beijing].

Dust intake is an important source of children's metal exposure. To explore the contamination level and health risk of toxic metals in kindergartens, surface dust samples were collected with self-made sampler in representative kindergartens in urban Beijing and concentrations of Pb, Hg, Cd, As were analyzed. It was found that Cd, Hg, Pb accumulated in indoor dust in different degrees with a significant seasonal variation. The geometric means of Pb, Cd, Hg, As concentrations were 63.12 microg x g(-1), 1.67 microg x g(-1), 0.06 microg x g(-1), 0.22 microg x g(-1) in summer and 117.40 microg x g(-1), 4.52 microg x g(-1), 0.95 microg x g(-1), 0.88 microg x g(-1) in winter, respectively. Geo-accumulation indexes calculated for each metal showed a severe contamination of Pb and Cd in indoor surface dusts. The results of exposure and health risk assessment of target substances displayed that the oral intake of dust metals was much higher than that of dermal pathways for children. However, no obvious carcinogenic and non-carcinogenic risks were found for all metals. The Pb, against other species, had the highest non-carcinogenic risk to children, Hazard Index of which was 0.12. Therefore, the health risk of Ph in indoor dust should raise the concern.