Direct Observation of Dynamic Bond Evolution in Single-Atom Pt/C3 N4 Catalysts.

Single-atom catalysts are promising platforms for heterogeneous catalysis, especially for clean energy conversion, storage, and utilization. Although great efforts have been made to examine the bonding and oxidation state of single-atom catalysts before and/or after catalytic reactions, when information about dynamic evolution is not sufficient, the underlying mechanisms are often overlooked. Herein, we report the direct observation of the charge transfer and bond evolution of a single-atom Pt/C3 N4 catalyst in photocatalytic water splitting by synchronous illumination X-ray photoelectron spectroscopy. Specifically, under light excitation, we observed Pt-N bond cleavage to form a Pt0 species and the corresponding C=N bond reconstruction; these features could not be detected on the metallic platinum-decorated C3 N4 catalyst. As expected, H2 production activity (14.7 mmol h-1 g-1 ) was enhanced significantly with the single-atom Pt/C3 N4 catalyst as compared to metallic Pt-C3 N4 (0.74 mmol h-1 g-1 ).

Mass spectrometry enumeration of filamentous M13 bacteriophage.

In the last decade, filamentous M13 bacteriophage has emerged into numerous biotechnological applications as a promising nontoxic and self-assembling biomaterial with specific binding properties. This raises a question about its upscale production that consequently requires an accurate phage enumeration during the various protocol developments. However, traditional methods of measuring phage concentration are mainly biological in nature and therefore time and labor intensive. These traditional methods also demonstrate poor reproducibility and are semi-quantitative at best. In the present work, we capitalized on mass spectrometry based absolute protein quantitation. We have optimized the quantitation conditions for a major coat protein, pVIII. Enumeration of M13 bacteriophage can be further performed using the determined molar concentration of pVIII, Avogadro's number, and known copy number of pVIII per phage. Since many different phages have well-defined copy number of capsid proteins, the proposed approach can be simply applied to any phage with known copy number of a specific capsid protein.

Fullerene-Directed Synthesis of Flowerlike Cu3(PO4)2 Crystals for Efficient Photocatalytic Degradation of Dyes.

Biomineralization is a typical methodology developed by nature to produce calcium-based materials. A method mimicking this process has nowadays become popular for the preparation of artificial organic-inorganic hybrids. Here, Cu3(PO4)2 crystals with a flowerlike morphology have been prepared using water-soluble derivatives of fullerene C60 as templates. In a typical system, flowerlike crystals of Cu3(PO4)2 (denoted FLCs-Cu) were obtained by simply dropping an aqueous solution of CuSO4 into phosphate-buffered saline (PBS) containing a highly water-soluble multiadduct of C60 (fullerenol). The best condition for the preparation of FLCs-Cu appeared at 0.20 mg·mL-1 fullerenol and 0.10 mol·L-1 PBS. During the formation of FLCs-Cu, fullerenol acts as a template and its content in FLCs-Cu is trace (less than 5% by atom) as confirmed by scanning electron microscopy mapping and thermogravimetric analysis. This feature makes fullerenol reusable, and the FLCs-Cu can be prepared repeatedly using the same fullerenol aqueous solution at least 10 times without a noticeable change in the morphology. The N2 adsorption/desorption isotherm showed that the doping of fullerenol increased the specific surface area of the Cu3(PO4)2 crystal. When fullerenol was replaced by C60 monoadducts that are cofunctionalized with a pyrrolidine cation and oligo(poly(ethylene oxide)) chains, FLCs-Cu can form as well, indicating that the strategy of using water-soluble C60 derivative as a template to get FLCs-Cu is universal. As a typical example of practical applications, the photocatalytic activity of the FLCs-Cu was investigated toward the degradation of dyes including rhodamine B and rhodamine 6G. In both cases, efficient photodegradation has been confirmed.

Single-Cell Mass Spectrometry of Subpopulations Selected by Fluorescence Microscopy.

Specific subpopulations in a heterogeneous collection of cells, for example, cancer stem cells in a tumor, are often associated with biological or medical conditions. Fluorescence microscopy, based on biomarkers labeled with fluorescent probes, is a widely used technique for the visualization and selection of such cells. Phenotypic differences for these subpopulations at the molecular level can be identified by their untargeted analysis by single-cell mass spectrometry (MS). Here, we combine capillary microsampling MS with fluorescence microscopy for the analysis of metabolite and lipid levels in single cells to discern the heterogeneity of subpopulations corresponding to mitotic stages. The distributions of ATP, reduced glutathione (GSH), and UDP- N-acetylhexosamine (UDP-HexNAc) levels in mitosis reveal the presence of 2-3 underlying subpopulations. Cellular energy is found to be higher in metaphase compared to prometaphase and slightly declines in anaphase, telophase, and cytokinesis. The [GTP]/[GDP] ratio in cytokinesis is significantly higher than in prometaphase and anaphase. Pairwise correlations between metabolite levels show that some molecules within a group, including certain amino acids and nucleotide sugars, are strongly correlated throughout mitosis, but this is not related to their pathway distances. Correlations are observed between monophosphates (AMP and GMP), diphosphates (ADP and GDP), and triphosphates (ATP and GTP) of different nucleosides. In contrast, there is low correlation between diphosphates and triphosphates of the same nucleoside (ADP and ATP).

Fullerenols Revisited: Highly Monodispersed Photoluminescent Nanomaterials as Ideal Building Blocks for Supramolecular Chemistry.

Fullerenols have been known for decades; however, the photoluminescent (PL) properties and applications in supramolecular chemistry of these molecules have not been well addressed. Herein, a strategy has been developed to purify the as-prepared fullerenols, and the photoluminescence and capabilities of these molecules to form supramolecular self-assemblies were systematically studied. It was found that fullerenols show wavelength-dependent emission with an absolute fluorescent quantum yield of approximately 3.5 %. The PL characteristics are reminiscent of carbon dots, especially those obtained by using the top-down method. The studied fullerenols can be used to detect Cu2+ ions with a limit of detection down to 3.50 µm. In addition, the amphiphilicity of the fullerenols can be readily tuned by ionic complexation with cationic surfactants, such as 1-tetradecyl-3-methylimidazoliumbromide (C14 mimB) and tetradecyltrimethylammonium bromide (TTAB). On increasing the concentration of the surfactant, the transition of aggregates was induced from highly ordered vesicles to honeycomb-structured crystals and finally to giant micelles. After the formation of supramolecular self-assemblies, enhancement of photoluminescence was observed, which can be ascribed to the suppression of intramolecular vibrations and motion combined with the loosely packed self-assembly array. This study provides a facile way to generate PL nanoarchitectures, which may find applications in fluorescent sensing, drug delivery, and optoelectronics.

Single-Cell Mass Spectrometry Approaches to Explore Cellular Heterogeneity.

Compositional diversity is a fundamental property in cell populations. Single-cell analysis promises new insight into this cellular heterogeneity on the genomic, transcriptomic, proteomic, and metabolomic levels. Mass spectrometry (MS) is a label-free technique that enables the multiplexed analysis of proteins, peptides, lipids, and metabolites in individual cells. The abundances of these molecular classes are correlated with the physiological states and environmental responses of the cells. In this Minireview, we discuss recent advances in single-cell MS techniques with an emphasis on sampling and ionization methods developed for volume-limited samples. Strategies for sample treatment, separation methods, and data analysis require special considerations for single cells. Ongoing analytical challenges include subcellular heterogeneity, non-normal statistical distributions of cellular properties, and the need for high-throughput, high molecular coverage and minimal perturbation.

Energy Charge, Redox State, and Metabolite Turnover in Single Human Hepatocytes Revealed by Capillary Microsampling Mass Spectrometry.

Metabolic analysis of single cells to uncover cellular heterogeneity and metabolic noise is limited by the available tools. In this study, we demonstrate the utility of capillary microsampling electrospray ionization mass spectrometry with ion mobility separation for nontargeted analysis of single cells. On the basis of accurate mass measurements and collision cross-section determination, a large number of chemical species, 22 metabolites and 54 lipids, were identified. To assess the cellular response to metabolic modulators, the adenylate energy charge (AEC) levels for control and rotenone treated cells were evaluated. A significant reduction in the AEC values was observed for rotenone treated cells. For the cells under oxidative stress, the mean value for the [reduced glutathione (GSH)]/[oxidized glutathione (GSSG)] ratio was significantly decreased, whereas the distribution of the [uridine diphosphate N-acetylhexosamine (UDP-HexNAc)]/[uridine diphosphate hexose (UDP-hexose)] ratio exhibited dramatic tailing to higher values. Lipid turnover rates were studied by pulse-chase experiments at the single cell level.

In situ metabolic analysis of single plant cells by capillary microsampling and electrospray ionization mass spectrometry with ion mobility separation.

Advances in single cell analysis techniques have demonstrated cell-to-cell variability in both homogeneous and heterogeneous cell populations strengthening our understanding of multicellular organisms and individual cell behaviour. However, additional tools are needed for non-targeted metabolic analysis of live single cells in their native environment. Here, we combine capillary microsampling with electrospray ionization (ESI) mass spectrometry (MS) and ion mobility separation (IMS) for the analysis of various single A. thaliana epidermal cell types, including pavement and basal cells, and trichomes. To achieve microsampling of different cell types with distinct morphology, custom-tailored microcapillaries were used to extract the cell contents. To eliminate the isobaric interferences and enhance the ion coverage in single cell analysis, a rapid separation technique, IMS, was introduced that retained ions based on their collision cross sections. For each cell type, the extracted cell material was directly electrosprayed resulting in ∼200 peaks in ESI-MS and ∼400 different ions in ESI-IMS-MS, the latter representing a significantly enhanced coverage. Based on their accurate masses and tandem MS, 23 metabolites and lipids were tentatively identified. Our results indicated that profound metabolic differences existed between the trichome and the other two cell types but differences between pavement and basal cells were hard to discern. The spectra indicated that in all three A. thaliana cell types the phenylpropanoid metabolism pathway had high coverage. In addition, metabolites from the subpathway, sinapic acid ester biosynthesis, were more abundant in single pavement and basal cells, whereas compounds from the kaempferol glycoside biosynthesis pathway were present at significantly higher level in trichomes. Our results demonstrate that capillary microsampling coupled with ESI-IMS-MS captures metabolic differences between A. thaliana epidermal cell types, paving the way for the non-targeted analysis of single plant cells and subcellular compartments.

Reversing electron transfer in a covalent triazine framework for efficient photocatalytic hydrogen evolution.

Covalent triazine-based frameworks (CTFs) have emerged as some of the most important materials for photocatalytic water splitting. However, development of CTF-based photocatalytic systems with non-platinum cocatalysts for highly efficient hydrogen evolution still remains a challenge. Herein, we demonstrated, for the first time, a one-step phosphidation strategy for simultaneously achieving phosphorus atom bonding with the benzene rings of CTFs and the anchoring of well-defined dicobalt phosphide (Co2P) nanocrystals (∼7 nm). The hydrogen evolution activities of CTFs were significantly enhanced under simulated solar-light (7.6 mmol h-1 g-1), more than 20 times higher than that of the CTF/Co2P composite. Both comparative experiments and in situ X-ray photoelectron spectroscopy reveal that the strong interfacial P-C bonding and the anchoring of the Co2P cocatalyst reverse the charge transfer direction from triazine to benzene rings, promote charge separation, and accelerate hydrogen evolution. Thus, the rational anchoring of transition-metal phosphides on conjugated polymers should be a promising approach for developing highly efficient photocatalysts for hydrogen evolution.

A compact pulsed power driver with precisely shaped current waveforms for magnetically driven loading experiments.

Magnetically driven loading techniques based on high current pulsed power drivers are very important tools for researching material dynamic behaviors and high-pressure physics. Based on the technologies of a Marx generator energy storage and low impedance coaxial cable energy transmission, a compact high current pulsed power driver CQ-7 was developed and established at the Institute of Fluid Physics, China Academy of Engineering Physics, which can generate precisely shaped current waveforms for magnetically driven loading experiments. CQ-7 is composed of 256 two-stage Marx generators in parallel with low impedance, high voltage coaxial cables for current output. The 256 Marx generators are divided into 16 groups, and each separate group can be individually triggered to discharge and shape currents in sequence by a low jitter, high voltage pulse trigger with 16 output signals. The electrical parameters of CQ-7 are a capacitance of 20.48 µF, an inductance of 4.12 nH, and a resistance of 3.35 mΩ in a short circuit. When working at the charging voltage of ±40-±60 kV, CQ-7 can deliver a peak current from 5 to 7 MA to the short-circuit loads with a rising time of 400-700 ns at different discharging time sequences. Two different experiments were conducted to test the performance of CQ-7: magnetically driven high velocity flyer plates and solid liner implosion. The results show that CQ-7 can accelerate the aluminum flyer plate with a size of 12 × 8 × 1 mm3 to more than 7.5 km/s and uniformly drive the aluminum liner with an inner diameter of 6.2 mm and a thickness of 0.4 mm to more than 9.5 km/s. Furthermore, these experiments indicate that CQ-7 is a robust platform for material dynamics and high-pressure physics.

Correction of coupled higher-order modes in the S-parameter characterization of wideband cavity beam position monitors.

Wideband RF cavity beam position monitors (CBPM) have been increasingly employed for short bunch interval operations in several linear accelerators. At a few nanoseconds of bunch spacing, the loaded quality factor of the CBPM TM110 dipole eigenmode is required to be sufficiently low to minimize the signal interference between consecutive bunches. Moreover, the bunched beam also couples to several unwanted higher-order modes (HOM), such as the TM210 and TE111 eigenmodes, which also may result in an error of the bunch position measurement if no precautions are taken. In the fabrication phase of CBPMs, the mode coupling can alter the TM110 mode frequency and therefore causes an error in its tuning, e.g., 0.3% for a 4.875 GHz CBPM with QL = 22.5. This error needs to be identified so that the precise tuning is enabled since the dipole mode frequency becomes critical for the position evaluations as the signal processing is relatively phase-sensitive. This paper presents an approach to extract the pure unperturbed frequency of the dipole mode, not altered by the response to coupled HOMs. An analytic model based on the superposition law applied to electromagnetic fields has been developed to characterize the response of coupled HOMs in the S-parameter measurement. The model has been further verified with numerical simulation in the CST-Studio software by analyzing an approximate single-mode response CBPM. The correction method was applied on a wideband CBPM prototype for the pre-research plan of future high repetition rate hard XFEL at the Chinese Academy of Engineering Physics.

Neuropeptide Localization in Lymnaea stagnalis: From the Central Nervous System to Subcellular Compartments.

Due to the relatively small number of neurons (few tens of thousands), the well-established multipurpose model organism Lymnaea stagnalis, great pond snail, has been extensively used to study the functioning of the nervous system. Unlike the more complex brains of higher organisms, L. stagnalis has a relatively simple central nervous system (CNS) with well-defined circuits (e.g., feeding, locomotion, learning, and memory) and identified individual neurons (e.g., cerebral giant cell, CGC), which generate behavioral patterns. Accumulating information from electrophysiological experiments maps the network of neuronal connections and the neuronal circuits responsible for basic life functions. Chemical signaling between synaptic-coupled neurons is underpinned by neurotransmitters and neuropeptides. This review looks at the rapidly expanding contributions of mass spectrometry (MS) to neuropeptide discovery and identification at different granularity of CNS organization. Abundances and distributions of neuropeptides in the whole CNS, eleven interconnected ganglia, neuronal clusters, single neurons, and subcellular compartments are captured by MS imaging and single cell analysis techniques. Combining neuropeptide expression and electrophysiological data, and aided by genomic and transcriptomic information, the molecular basis of CNS-controlled biological functions is increasingly revealed.

Identification of Metabolites in Single Cells by Ion Mobility Separation and Mass Spectrometry.

Non-targeted metabolic analysis of single cells by mass spectrometry (MS) is important for understanding individual cell functions and characterizing cell-to-cell heterogeneity. However, identifying biomolecules in single cells presents significant challenges due to the low picoliter volume samples and the structural diversity of metabolites. Capillary microsampling electrospray ionization (ESI) MS with ion mobility separation (IMS) enables the analysis of single cells under ambient conditions with minimum sample pretreatment and improved specificity. Here, we describe a protocol for the analysis of the metabolic makeup, and the identification of ions produced from single cells by capillary microsampling ESI-IMS-MS.

Quantitative Proteomic Analysis of Biogenesis-Based Classification for Extracellular Vesicles.

Extracellular vesicles (EVs) are traditionally divided into two major groups: (i) large vesicles originating from plasma membrane and called microvesicles, and (ii) small vesicles originating from the endoplasmic membrane and called exosomes. However, it is increasingly clear that the actual composition of a particular EV preparation cannot be adequately described with these two simple terms and is much more complex. Since the cell membrane origin of EVs predetermines their biological functions, the understanding of EV biogenesis is important for accurate interpretation of observed results. In the present study, we propose to take advantage of selective expression of some proteins in plasma or endosomal membranes and to use these proteins as plasma membrane-specific or endosomal membrane-specific markers. We have demonstrated that a quantitative mass spectrometry analysis allows simultaneous measurement of plasma membrane-specific and endosomal membrane-specific proteins in microvesicles and exosomes obtained after differential ultracentrifugation. Before mass spectrometry analysis, we also used sonicated platelets as a model of mixed EVs and multidetector asymmetrical-flow field-flow fractionation as an analytical method to verify a possible cross contamination of obtained microvesicles and exosomes. Based on the quantitative appearance of membrane-specific protein markers in EV preparations from human plasma and from human ARPE-19 cell medium, we concluded that there is no actual size limitation and both microvesicles and exosomes can be represented by large and small vesicles.

Photoluminescent and pH-responsive supramolecular structures from co-assembly of carbon quantum dots and zwitterionic surfactant micelles.

The co-assembly of negatively charged carbon quantum dots (CQDs) and a zwitterionic surfactant (tetradecyldimethylamine oxide, C14DMAO) in water has been investigated, which results in the formation of a new class of photoluminescent and pH-responsive self-assemblies. Instead of a direct binding mode, the surfactant unimers self-associate into micelles before interacting with the CQDs. Each of the micelles carries a small amount of positive charge due to the partial protonation of C14DMAO (C14DMAO + H+ = C14DMAOH+). For aqueous solutions containing 0.1 mg mL-1 CQDs, two types of structures have been confirmed upon the addition of C14DMAO, i.e., supramolecular polymers and vesicles. Between them, a variety of intermediate structures are observed, including ribbons, oligomers of vesicles and helixes. Due to the reversible protonation/deprotonation of the zwitterionic surfactant, both the supramolecular polymers and vesicles exhibit reversible changes toward the variation of pH, providing opportunities to facilely adjust their properties wherever necessary. As the CQDs evenly distribute in the micelle matrix, the self-quenching of the CQDs has been significantly suppressed and their photoluminescence has been well preserved. The supramolecular polymers have been further selected as hosts to accommodate rhodamine 6G, which is used as a model drug, and the controlled release stimulated by pH has been realized.

Note: Stability and lifetime of scandium deuteride film cathode in a vacuum arc ion source.

This paper reports the properties of the plasma and gas produced in a vacuum arc discharge with scandium deuteride (ScD1.8) film cathodes. The thickness of the ScD1.8 film influences the quantity of the gases released from the cathode material. The deuterium gas releasing in the discharge process was in a depth range from the cathode surface to the cathode interior, that is, between 3 and 6 µm. Surprisingly, after discharge, the deuterium ion ratio remains the same in the film with different thicknesses. That indicates that the release of deuterium gas in a 3 µm-thick ScD1.8 film is enough for ionization. In addition, as the number of discharge increases, the stability of atomic fraction ratio gets worse and the ratio of deuterium ions decreases.

Subcellular Peptide Localization in Single Identified Neurons by Capillary Microsampling Mass Spectrometry.

Single cell mass spectrometry (MS) is uniquely positioned for the sequencing and identification of peptides in rare cells. Small peptides can take on different roles in subcellular compartments. Whereas some peptides serve as neurotransmitters in the cytoplasm, they can also function as transcription factors in the nucleus. Thus, there is a need to analyze the subcellular peptide compositions in identified single cells. Here, we apply capillary microsampling MS with ion mobility separation for the sequencing of peptides in single neurons of the mollusk Lymnaea stagnalis, and the analysis of peptide distributions between the cytoplasm and nucleus of identified single neurons that are known to express cardioactive Phe-Met-Arg-Phe amide-like (FMRFamide-like) neuropeptides. Nuclei and cytoplasm of Type 1 and Type 2 F group (Fgp) neurons were analyzed for neuropeptides cleaved from the protein precursors encoded by alternative splicing products of the FMRFamide gene. Relative abundances of nine neuropeptides were determined in the cytoplasm. The nuclei contained six of these peptides at different abundances. Enabled by its relative enrichment in Fgp neurons, a new 28-residue neuropeptide was sequenced by tandem MS.

Effect of progesterone and its synthetic analogs on reproduction and embryonic development of a freshwater invertebrate model.

The presence of a mixture of progestogens at ng/L concentration levels in surface waters is a worldwide problem. Only a few studies explore the effect of progestogen treatment in a mixture as opposed to individual chemicals to shed light on how non-target species respond to these contaminants. In the present study, we used an invertebrate model species, Lymnaea stagnalis, exposed to a mixture of four progestogens (progesterone, levonorgestrel, drospirenone, and gestodene) in 10ng/L concentration for 3 weeks. Data at both physiological and cellular/molecular level were analyzed using the ELISA technique, stereomicroscopy combined with time lapse software, and capillary microsampling combined with mass spectrometry. The treatment of adult Lymnaeas caused reduced egg production, and low quality egg mass on the first week, compared to the control. Starting from the second week, the egg production, and the quality of egg mass were similar in both groups. At the end of the third week, the egg production and the vitellogenin-like protein content of the hepatopancreas were significantly elevated in the treated group. At the cellular level, accelerated cell proliferation was observed during early embryogenesis in the treated group. The investigation of metabolomic changes resulted significantly elevated hexose utilization in the single-cell zygote cytoplasm, and elevated adenylate energy charge in the egg albumen. These changes suggested that treated snails provided more hexose in the eggs in order to improve offspring viability. Our study contributes to the knowledge of physiological effect of equi-concentration progestogen mixture at environmentally relevant dose on non-target aquatic species.

Diffusion and distribution of deuterium in scandium deuteride thin films under irradiation of deuterium ion beam.

Scandium deuteride (ScDx) thin films, as an alternative target for deuterium-deuterium (D-D) reaction, are a very important candidate for detection and diagnostic applications. Albeit with their superior thermal stability, the ignorance of the stability of ScDx under irradiation of deuterium ion beam hinders the realization of their full potential. In this report, we characterize ScDx thin films with scanning electron microscopy (SEM) and X-ray diffraction (XRD), Rutherford backscattering spectroscopy (RBS) and elastic recoil detection analysis (ERDA). We found with increased implantation of deuterium ions, accumulation and diffusion of deuterium are enhanced. Surprisingly, the concentration of deuterium restored to the value before implantation even at room temperature, revealing a self-healing process which is of great importance for the long-term operation of neutron generator.

Coupling and decoupling of the accelerating units for pulsed synchronous linear accelerator.

A pulsed synchronous linear accelerator (PSLA), based on the solid-state pulse forming line, photoconductive semiconductor switch, and high gradient insulator technologies, is a novel linear accelerator. During the prototype PSLA commissioning, the energy gain of proton beams was found to be much lower than expected. In this paper, the degradation of the energy gain is explained by the circuit and cavity coupling effect of the accelerating units. The coupling effects of accelerating units are studied, and the circuit topologies of these two kinds of coupling effects are presented. Two methods utilizing inductance and membrane isolations, respectively, are proposed to reduce the circuit coupling effects. The effectiveness of the membrane isolation method is also supported by simulations. The decoupling efficiency of the metal drift tube is also researched. We carried out the experiments on circuit decoupling of the multiple accelerating cavity. The result shows that both circuit decoupling methods could increase the normalized voltage.