Molecular Nature Research Articles

Potassium extrusion by plant cells: evolution from an emergency valve to a driver of long-distance transport.

The ability to accumulate nutrients is a hallmark for living creatures and plants evolved highly effective nutrient transport systems, especially for the uptake of potassium (K+). However, plants also developed mechanisms that enable the rapid extrusion of K+ in combination with anions. The combined release of K+ and anions is probably an ancient extrusion system, as it is found in the Characeae that are closely related to land plants. We postulate that the ion extrusion mechanisms have developed as an emergency valve, which enabled plant cells to rapidly reduce their turgor, and prevent them from bursting. Later in evolution, seed plants adapted this system for various responses, such as the closure of stomata, long-distance stress waves, dropping of leaves by pulvini, and loading of xylem vessels. We discuss the molecular nature of the transport proteins that are involved in ion extrusion-based functions of plants and describe the functions that they obtained during evolution.

Synergistic Electronic and Carbonyl Proximity Effects in Electrochemical Hydrogen Evolution Catalyzed by Tetrakis(ethoxycarbonyl)porphyrin Metal Complexes

Abstract Electrocatalytic properties of a series of tetrakis(ethoxycarbonyl)porphyrin (TECP) 3d-metal complexes, and the influence of ester groups on the hydrogen evolution reaction (HER), were investigated using trifluoroacetic acid in a 0.1 M [Bu4N]PF6 DMF solution. [Co(TECP)], [Ni(TECP)], and [Cu(TECP)] exhibited three redox couples, with reversibility decreasing at more negative potentials. The third reduction couple was predominantly ligand-centered. Upon addition of TFA, the second reduction waves became catalytic, increasing proportionally with TFA concentration, indicating that the molecular nature of the [M(TECP)] complexes plays a role in facilitating HER. Electrochemical and catalytic studies revealed that [Cu(TECP)] demonstrated the highest Faradaic efficiency (FE) of 98% and the lowest overpotential (0.7 V) while maintaining strong acid tolerance. [Co(TECP)] became effective at overpotentials exceeding 800 mV, suggesting the predominance of EECC pathway at more negative potential. The roles of the ester groups extended beyond a simple inductive effect, as confirmed by controlled potential electrolysis and spectroelectrochemical analyses. The superior HER activity of [Cu(TECP)] compared to [Cu(TPrP)] and [Cu(TPP)] highlights the contribution of the carbonyl groups to catalytic performance. This work underscores the importance of ester groups placement within the porphyrin framework and suggests that meso-ester groups can influence both the stability and catalytic performance, paving the way for further investigations

Einstein–Perrin dilemma on the Brownian motion (Avogadro’s number) resolved?

The general recognition of the existence of atoms and molecules occurred only at the beginning of the twentieth century. Many researchers contributed to this, but the ultimate proof of the molecular nature of matter that convinced even the last sceptics was the confirmation of Albert Einstein’s statistical-fluctuation theory of Brownian motion, a part of his comprehension of interdisciplinary atomism, by Jean Perrin’s experiments on colloidal gamboge particles. Einstein noticed a difference between the values of Avogadro’s constant derived from Perrin’s experiments and Planck’s calculation from black-body radiation. Einstein assumed the incorrectly evaluated size of the gamboge spherules to be a culprit of the difference and asked Perrin to check the assumption with additional experiments and using the viscosity formula introduced in his own dissertation. The result was a discrepancy that neither Einstein nor Perrin settled any further. In this communication, based on the survey of developments in colloid and polymer science and their comparison with relevant experiments, an explanation of the dilemma is given that now, after more than a century, proves Einstein correct. The comparison was de facto possible during his lifetime.

Promising tools for future drug discovery and development in antiarrhythmic therapy.

Arrhythmia refers to irregularities in the rate and rhythm of the heart, with symptoms spanning from mild palpitations to life-threatening arrhythmias and sudden cardiac death (SCD). The complex molecular nature of arrhythmias complicates the selection of appropriate treatment. Current therapies involve the use of antiarrhythmic drugs (class I-IV) with limited efficacy and dangerous side effects and implantable pacemakers and cardioverter-defibrillators with hardware-related complications and inappropriate shocks. The number of novel antiarrhythmic drug in the development pipeline has decreased substantially during the last decade and underscores uncertainties regarding future developments in this field. Consequently, arrhythmia treatment poses significant challenges, prompting the need for alternative approaches. Remarkably, innovative drug discovery and development technologies show promise in helping advance antiarrhythmic therapies. Here, we review unique characteristics and the transformative potential of emerging technologies that offer unprecedented opportunities for transitioning from traditional antiarrhythmics to next-generation therapies. We assess stem cell technology, emphasizing the utility of innovative cell profiling using multi-omics, high-throughput screening, and advanced computational modeling in developing treatments tailored precisely to individual genetic and physiological profiles. We offer insights into gene therapy, peptide and peptibody approaches for drug delivery. We finally discuss potential strengths and weaknesses of such techniques in reducing adverse effects and enhancing overall treatment outcomes, leading to more effective, specific, and safer therapies. Altogether, this comprehensive overview introduces innovative avenues for personalized rhythm therapy, with particular emphasis on drug discovery, aiming to advance the arrhythmia treatment landscape and the prevention of SCD. Significance Statement Arrhythmias and sudden cardiac death account for 15-20% of deaths worldwide. However, current antiarrhythmic therapies are ineffective and with dangerous side effects. Here, we review the field of arrhythmia treatment underscoring the slow progress in advancing the cardiac rhythm therapy pipeline and the uncertainties regarding evolution of this field. We provide information on how emerging technological and experimental tools can help accelerate progress and address the limitations of antiarrhythmic drug discovery.

Contribution of specific extracellular organic matter on membrane fouling in ultrafiltration and coagulation-ultrafiltration of algae-laden water

This study explores the specific impact of bound and dissolved extracellular organic matter (bEOM and dEOM), and their collective influence with algal cells on membrane fouling during ultrafiltration (UF) and coagulation-UF of algae-laden water. By characterizing the organic properties and adsorptive behaviors of bEOM and dEOM, and analyzing their subsequent impacts, we clarify their roles and contributions to membrane fouling. Our analyses revealed that bEOM, characterized by its higher molecular weight (MW) and hydrophobic nature, contains more protein-like substances compared to dEOM. Quartz Crystal Microbalance with Dissipation (QCM-D) analysis highlights significant differences in their adsorption behaviors, with bEOM demonstrating greater adhesion and higher adsorptive fouling potential. Despite bEOM's lower concentration relative to dEOM, at a ratio of 0.12–1, their contributions to irreversible membrane resistance are nearly identical, at 30.7% and 30.9% respectively, in the UF of algae-laden water. Coagulation pretreatment effectively reduces bEOM's fouling potential by forming larger flocs, thus minimizing its contact with the membrane. In terms of irreversible membrane resistance, the contributions are 6.5% from cells, 24.8% from bEOM, and 68.6% from dEOM. The presence of dEOM complicates coagulation efficiency due to its low MW components and high hydrophilicity. Using the Hermia model, atomic force microscopy (AFM), and scanning electron microscopy (SEM), we demonstrated how bEOM and dEOM modify membrane fouling mechanisms, particularly by influencing cake layer formation. These insights emphasize the distinct and significant contributions of bEOM and dEOM to membrane fouling, necessitating targeted strategies for their management to enhance the efficiency and sustainability of UF systems in water treatment facilities.

Cytoplasmic strings in human blastocysts: hypotheses of their role and implications for embryo selection.

What are the implications of the presence cytoplasmic strings (Cyt-S) and their quantity and dynamics for the pre-implantation development of human blastocysts? Cyt-S are common in human embryos and are associated with faster blastocyst development, larger expansion, and better morphological quality. Cyt-S are dynamic cellular projections connecting inner cell mass and trophectoderm (TE) cells, that can be observed during blastocyst expansion. Their prevalence in human embryos has been estimated to be between 44% and 93%. Data relevant to their clinical implications and role in development are lacking, limited, or controversial. Retrospective study conducted at a single IVF center between May 2013 and November 2014 and involving 124 pre-implantation genetic testing for aneuploidy cycles in a time-lapse incubator with ≥1 blastocyst biopsied and vitrified (N = 370 embryos assessed). These cycles resulted in 87 vitrified-warmed single-euploid blastocyst transfers. ICSI, continuous blastocyst culture (Days 5-7), TE biopsy of fully expanded blastocysts without Day 3 zona pellucida drilling, qPCR to assess uniform full-chromosome aneuploidies, and vitrification were all performed. Only vitrified-warmed euploid single-embryo-transfers were conducted. Blastocyst morphological quality was defined according to Gardner's criteria. The AI-based software CHLOE™ (Fairtility) automatically registered timings from time of starting blastulation (tSB) to biopsy (t-biopsy, i.e. blastocyst full-expansion) as hours-post-insemination (hpi), embryo area (including zona pellucida in µm2), and spontaneous blastocyst collapses. One senior embryologist manually annotated Cyt-S presence, quantity, timings, and type (thick cell-to-cell connections and/or threads). All significant associations were confirmed through regression analyses. All couples', cycles', and embryos' main features were also tested for associations with Cyt-S presence, quantity, and dynamics. About 94.3% of the patients (N = 117/124) had ≥1 embryo with Cyt-S. Out of a total of 370 blastocysts, 55 degenerated between blastulation and full-expansion (N = 55/370, 14.9%). The degeneration rate among embryos with ≥1 Cyt-S was 10.8% (N = 33/304), significantly lower than that of embryos without Cyt-S (33.3%, N = 22/66, P < 0.01). Of the remaining 315 viable blastocysts analyzed, 86% (N = 271/315; P < 0.01) had ≥1 Cyt-S, on average 3.5 ± 2.1 per embryo ranging 1-13. The first Cyt-S per viable embryo appeared at 115.3 ± 12.5 hpi (85.7-157.7), corresponding to 10.5 ± 5.8 h (0.5-31) after tSB. Overall, we analyzed 937 Cyt-S showing a mean duration of 3.8 ± 2.7 h (0.3-20.9). Cyt-S were mostly threads (N = 508/937, 54.2%) or thick cell-to-cell connections becoming threads (N = 382/937, 40.8%) than thick bridges (N = 47/937, 5.0%). The presence and quantity of Cyt-S were significantly associated with developmentally faster (on average 6-12 h faster) and more expanded (on average 2700µm2-larger blastocyst's area at t-biopsy) embryos. Also, the presence and duration of Cyt-S were associated with better morphology. Lastly, while euploidy rates were comparable between blastocysts with and without Cyt-S, all euploid blastocysts transferred from the latter group failed to implant (N = 10). Cyt-S presence and dynamics were assessed manually on seven focal planes from video frames recorded every 15 min. The patients included were mostly of advanced maternal age. Only associations could be reported, but no causations/consequences. Lastly, larger datasets are required to better assess Cyt-S associations with clinical outcomes. Cyt-S are common during human blastocyst expansion, suggesting their physiological implication in this process. Their presence, quantity and dynamics mirror embryo viability, and morphological quality, yet their role is still unknown. Future basic science studies are encouraged to finally describe Cyt-S molecular nature and biophysical properties, and Artificial Intelligence tools should aid these studies by incorporating Cyt-S assessment. None. N/A.

Excess Molar Volume and Deviations in Viscosity of the Binary Liquid Mixtures Containing 1,3-Dioxolane + Alkanols at T = 298.15k

Thermodynamic and transport properties of liquid and liquid mixtures have been used to understand the intermolecular interactions between the components of the mixture. The sound velocity, density and viscosity of binary liquid mixtures are important from practical and theoretical point of view to understand the liquid theory. In the present study sound velocity, density and viscosity have been measured of binary mixtures of 1, 3-dioxolane with pentanol, hexanol, heptanol, octanol, nonanol and decanol over the entire range of mole fraction at 298.15K, and atmospheric pressure. From these experimental measurements the excess molar volume (V&amp;lt;sub&amp;gt;m&amp;lt;/sub&amp;gt;&amp;lt;SUP&amp;gt;E&amp;lt;/SUP&amp;gt;), excess viscosity (η&amp;lt;SUP&amp;gt;E&amp;lt;/SUP&amp;gt;), acoustic impedance (Z&amp;lt;SUP&amp;gt;E&amp;lt;/SUP&amp;gt;) and excess adiabatic compressibility (β&amp;lt;sub&amp;gt;ad&amp;lt;/sub&amp;gt;&amp;lt;SUP&amp;gt;E&amp;lt;/SUP&amp;gt;), have been calculated. The excess molar volume (V&amp;lt;sub&amp;gt;m&amp;lt;/sub&amp;gt;&amp;lt;SUP&amp;gt;E&amp;lt;/SUP&amp;gt;), excess viscosity (η&amp;lt;SUP&amp;gt;E&amp;lt;/SUP&amp;gt;), acoustic impedance (Z&amp;lt;SUP&amp;gt;E&amp;lt;/SUP&amp;gt;) and excess adiabatic compressibility (β&amp;lt;sub&amp;gt;ad&amp;lt;/sub&amp;gt;&amp;lt;SUP&amp;gt;E&amp;lt;/SUP&amp;gt;), have been analyzed in terms of interactions arising due to structural effect, charge-transfer complexes and dipole-dipole interaction between unlike molecules. These deviations have been correlated by a polynomial Redlich-Kister equation. The excess properties are found to be eighter negative or positive depending on the molecular interactions and nature of the liquid mixtures. Excess properties provide important information in understanding the solute-solvent interaction in a solution. The excess molar volume (V&amp;lt;sub&amp;gt;m&amp;lt;/sub&amp;gt;&amp;lt;SUP&amp;gt;E&amp;lt;/SUP&amp;gt;), excess viscosity (η&amp;lt;SUP&amp;gt;E&amp;lt;/SUP&amp;gt;), acoustic impedance (Z&amp;lt;SUP&amp;gt;E&amp;lt;/SUP&amp;gt;) and excess adiabatic compressibility (β&amp;lt;sub&amp;gt;ad&amp;lt;/sub&amp;gt;&amp;lt;SUP&amp;gt;E&amp;lt;/SUP&amp;gt;), values have been interpreted to terms of the nature of intermolecular interactions between constituent molecules of mixtures.

Reconstructing of the geometry of Atg13 and Atg101 molecules while assembling the complex

Aim. Associated subproteins which constitute the ATG1 multi-protein complex in plants and mammals, including ULK1 in humans, are orchestral protein kinase atg-units in resistance to stress stimuli across their different nature. The goals of this endeavour were to characterize the molecular nature of the interaction of ATG13 with ATG101, followed by in silico docking to catch the plausible ensuing integration into a multimeric complex ULK1/ATG1, which initiates the assembly of a PAS-preautophagosomal structure in the first step of autophagy initiation. Methods. Protein structures were modeled by homology using AlphaFold, and molecular dynamics (MD) was performed using GROMACS 5.0 with the Charmm36. Results. By implementing computer modeling methods, a complex of protein kinase atg-units for both ATG13 and ATG101 proteins, reflecting the interaction interface and conformational properties, was constructed for detailed interpretation while forming the forthcoming assembly of the ULK1/ATG1 multi-protein platform. Conclusions. This study provides a high-quality model platform for further sequential studies of protein-protein docking and protein-protein interactions with the possibility of reconstructing a model of the full ULK1/ATG1 complex to identify ATG8 binding sites.

Milling-Induced "Turn-off" Luminescence in Copper Nanoclusters.

Atomically precise copper nanoclusters (NCs) attract research interest due to their intense photoluminescence, which enables their applications in photonics, optoelectronics, and sensing. Exploring these properties requires carefully designed clusters with atomic precision and a detailed understanding of their atom-specific luminescence properties. Here, we report two copper NCs, [Cu4(MNA)2(DPPE)2] and [Cu6(MNA-H)6], shortly Cu4 and Cu6, protected by 2-mercaptonicotinic acid (MNA-H2) and 1,2-bis(diphenylphosphino)ethane (DPPE), showing "turn-off" mechanoresponsive luminescence. Single-crystal X-ray diffraction reveals that in the Cu4 cluster, two Cu2 units are appended with two thiols, forming a flattened boat-shaped Cu4S2 kernel, while in the Cu6 cluster, two Cu3 units form an adamantane-like Cu6S6 kernel. High-resolution electrospray ionization mass spectrometry studies reveal the molecular nature of these clusters. Lifetime decay profiles of the two clusters show the average lifetimes of 0.84 and 1.64 μs, respectively. These thermally stable Cu NCs become nonluminescent upon mechanical milling but regain their emission upon exposure to solvent vapors. Spectroscopic data of the clusters match well with their computed electronic structures. This work expands the collection of thermally stable and mechanoresponsive luminescent coinage metal NCs, enriching the diversity and applications of such materials.

The Molecular Nature of Redox-Conductive Metal-Organic Frameworks.

ConspectusRedox-conductive metal-organic frameworks (RC-MOFs) are a class of porous materials that exhibit electrical conductivity through a chain of self-exchange reactions between molecularly defined, neighboring redox-active units of differing oxidation states. To maintain electroneutrality, this electron hopping transport is coupled to the translocation of charge balancing counterions. Owing to the molecular nature of the redox active components, RC-MOFs have received increasing attention for potential applications in energy storage, electrocatalysis, reconfigurable electronics, etc. While our understanding of fundamental aspects that govern electron hopping transport in RC-MOFs has improved during the past decade, certain fundamental aspects such as questions that arise from the coupling between electron hopping and diffusion migration of charge balancing counterions are still not fully understood.In this Account, we summarize and discuss our group's efforts to answer some of these fundamental questions while also demonstrating the applicability of RC-MOFs in energy-related applications. First, we introduce general design strategies for RC-MOFs, fundamentals that govern their charge transport properties, and experimental diagnostics that allow for their identification. Selected examples with redox-active organic linkers or metallo-linkers are discussed to demonstrate how the molecular characteristics of the redox-active units inside RC-MOFs are retained. Second, we summarize experimental techniques that can be used to characterize charge transport properties in a RC-MOF. The apparent electron diffusion coefficient, Deapp, that is frequently determined in the field and obtained in large perturbation, transient experiments will be discussed and related to redox conductivity, σ, that is obtained in a steady state setup. It will be shown that both MOF-intrinsic (topology, pore size, and apertures) and experimental (nature of electrolyte, solvent) factors can have noticeable impact on electrical conductivity through RC-MOFs. Lastly, we summarize our progress in utilizing RC-MOFs as electrochromic materials, materials for harvesting minority carriers from illuminated semiconductors and within electrocatalysis. In the latter case, recent work on multivariate RC-MOFs in which redox active linkers are used to "wire" redox catalysts in the crystal interiors will be presented, offering opportunities to independently optimize charge transport and catalytic function.The ambition of this Account is to inspire the design of new RC-MOF systems, to aid their identification, to provide mechanistic insights into the governing ion-coupled electron hopping transport mode of conductivity, and ultimately to promote their applications in existing and emerging areas. With basically unlimited possibilities of molecular engineering tools, together with research in both fundamental and applied fields, we believe that RC-MOFs will attract even more attention in the future to unlock their full potential.

Heterogeneous Photo-Fenton Degradation of Azo Dyes over a Magnetite-Based Catalyst: Kinetic and Thermodynamic Studies

Textile wastewater containing dyes poses significant environmental hazards. Advanced oxidative processes, especially the heterogeneous photo-Fenton process, are effective in degrading a wide range of contaminants due to high conversion rates and ease of catalyst recovery. This study evaluates the heterogeneous photodegradation of the azo dyes Acid Red 18 (AR18), Acid Red 66 (AR66), and Orange 2 (OR2) using magnetite as a catalyst. The magnetic catalyst was synthesized via a hydrothermal process at 150 °C. Experiments were conducted at room temperature, investigating the effect of catalyst dosage, pH, and initial concentrations of H2O2 and AR18 dye. Kinetic and thermodynamic studies were performed at 25, 40, and 60 °C for the three azo dyes (AR18, AR66, and OR2) and the effect of the dye structures on the degradation efficiency was investigated. At 25 °C for 0.33 mmolL−1 of dye at pH 3.0, using 1.4 gL−1 of the catalyst and 60 mgL−1 of H2O2 under UV radiation of 16.7 mWcm−2, the catalyst showed 62.3% degradation for AR18, 79.6% for AR66, and 83.8% for OR2 in 180 min of reaction. The oxidation of azo dyes under these conditions is spontaneous and endothermic. The pseudo-first-order kinetic constants indicated a strong temperature dependence with an order of reactivity of the type OR2 &gt; AR66 &gt; AR18, which is associated with the molecular size, steric hindrance, aromatic conjugation, electrostatic repulsion, and nature of the acid–base interactions on the catalytic surface.

A structural determinant of the behavior of water at hydration and nanoconfinement conditions.

The molecular nature of the phases that conform the two-liquid scenario is elucidated in this work in the light of a molecular principle governing water structuring, which unveils the relevance of the contraction and reorientation of the second molecular shell to allow for the existence of coordination defects in water's hydrogen bond network. In turn, such principle is shown to also determine the behavior of hydration and nanoconfined water while enabling to define conditions for wettability (quantifying hydrophobicity and predicting drying transitions), thus opening the possibility to unravel the active role of water in central fields of research.

Large TRAPPC11 gene deletions as a cause of muscular dystrophy and their estimated genesis

BackgroundTransport protein particle (TRAPP) is a multiprotein complex that functions in localising proteins to the Golgi compartment. The TRAPPC11 subunit has been implicated in diseases affecting muscle, brain, eye and...

Predicting isovector charmonium-like states from X(3872) properties

Using chiral effective field theory, we predict that there must be isovector charmonium-like DD¯∗\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ D{\\overline{D}}^{\\ast } $$\\end{document} hadronic molecules with JPC = 1++ denoted as Wc1. The inputs are the properties of the X(3872), including its mass and the ratio of its branching fractions of decays into J/ψρ0 and J/ψω. The predicted states are virtual state poles of the scattering matrix, pointing at a molecular nature of the X(3872) as well as its spin partners. They should show up as either a mild cusp or dip at the DD¯∗\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ D{\\overline{D}}^{\\ast } $$\\end{document} thresholds, explaining why they are elusive in experiments. The so far negative observation also indicates that the X(3872) is either a bound state with non-vanishing binding energy or a virtual state, only in these cases the X(3872) signal dominates over that from the Wc10\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ {W}_{c1}^0 $$\\end{document}. The pole positions are 3881.2−0.0+0.8\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ {3881.2}_{-0.0}^{+0.8} $$\\end{document}−i1.6−0.9+0.7\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ i{1.6}_{-0.9}^{+0.7} $$\\end{document} MeV for Wc10\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ {W}_{c1}^0 $$\\end{document} on the fourth Riemann sheet of the D0D¯∗0\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ {D}^0{\\overline{D}}^{\\ast 0} $$\\end{document}-D+D∗− coupled-channel system, and 3866.9−7.7+4.6\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ {3866.9}_{-7.7}^{+4.6} $$\\end{document}− i(0.07 ± 0.01) MeV for Wc1±\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ {W}_{c1}^{\\pm } $$\\end{document} on the second Riemann sheet of the DD¯∗±\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ {\\left(D{\\overline{D}}^{\\ast}\\right)}^{\\pm } $$\\end{document} single-channel system. The findings imply that the peak in the J/ψπ+π− invariant mass distribution is not purely from the X(3872) but contains contributions from Wc10\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ {W}_{c1}^0 $$\\end{document} predicted here. The states should have isovector heavy quark spin partners with JPC = 0++, 2++ and 1+−, with the last one corresponding to Zc. We suggest to search for the charged 0++, 1++ and 2++ states in J/ψπ±π0.

Production of Lactic Acid via Catalytic Transfer Dehydrogenation of Glycerol Catalyzed by Base Metal Salt Ferrous Chloride and Its NNN Pincer-Iron Complexes.

NNN-Bis(imino) pyridine-based pincer-Fe(II) complexes with an expected trigonal bipyramidal (TBP) geometry equilibrated to a rearranged ion pair of an octahedral dicationic Fe complex containing two bis(imino)pyridine ligands that are neutralized by a tetrahedral dianionic-[FeCl4]2-. Single-crystal X-ray diffraction (SCXRD), high-resolution mass spectrometry (HRMS), and UV-visible (UV-vis) studies suggested that the equilibrium was dictated by the sterics of the R group on the imine N, with the less-crowded groups tilting the equilibrium to the ion pair and the bulky ones favoring the TBP geometry. Electron paramagnetic resonance (EPR) and Evan's magnetic moment measurements indicated that the complexes were paramagnetic with Fe(II) in a high-spin state. In solution, over a period of 7 days, these Fe(II) complexes oxidized to a mixture of low-spin and high-spin Fe(III) species. These pincer-Fe(II) were found to be highly active toward the transformation of biodiesel waste glycerol to value-added lactic acid (LA). Particularly, (Ph2NNN)FeCl2 (0.1 mol %) gave 91% LA with a 99% selectivity at 140 °C using 1.2 equiv of NaOH. With 0.0001 mol % (Ph2NNN)FeCl2, very high turnovers (74% LA, 98% selectivity, 740 000 turnover number (TON) at 4405 turnovers per hour (TOs/h)) were obtained after 7 days. EPR indicated Fe(III) species to be the active catalyst, a few of which were detected by HRMS. Experiments with Hg are suggestive of the mostly homogeneous molecular nature of the catalyst with a minor contribution from heterogeneous Fe nanoparticles.

Rare earth metallic elements in plants: assessing benefits, risks and mitigating strategies.

Rare earth elements (REEs) comprises of a uniform group of lanthanides and scandium (Sc) and yttrium (Y) finding their key importance in agriculture sectors, electronic and defense industries, and renewable energy production. The immense application of REEs as plant growth promoters has led to their undesirable accumulation in the soil system raising concerns for REE pollution as upcoming stresses. This review mainly addresses the chemistry of REEs, uptake and distribution and their biphasic responses in plant systems and possible plausible techniques that could mitigate/alleviate REE contamination. It extends beyond the present understanding of the biphasic impacts of rare earth elements (REEs) on physio-biochemical attributes. It not only provides landmarks for further exploration of the interrelated phytohormonal and molecular biphasic nature but also introduces novel approaches aimed at mitigating their toxicities. By delving into innovative strategies such as recycling, substitution, and phytohormone-assisted mitigation, the review expands upon existing knowledge of REEs whilst also offering pathways to tackle the challenges associated with REE utilization.

A plastic aggrecan barrier modulated by peripheral energy state gates metabolic signal access to arcuate neurons

The hypothalamic arcuate nucleus (ARH) contains neurons vital for maintaining energy homeostasis that sense and respond to changes in blood-borne metabolic hormones. Despite its juxtaposition to the median eminence (ME), a circumventricular organ lacking a blood-brain barrier and thus exposed to circulating molecules, only a few ventral ARH neurons perceive these extravasating metabolic signals due to a poorly understood ME/ARH diffusion barrier. Here, we show in male mice that aggrecan, a perineural-net proteoglycan deposited by orexigenic ARH neurons, creates a peculiar ventrodorsal diffusion gradient. Fasting enhances aggrecan deposition more dorsally, reinforcing the diffusion barrier, particularly around neurons adjacent to fenestrated capillary loops that enter the ARH. The disruption of aggrecan deposits results in unregulated diffusion of blood-borne molecules into the ARH and impairs food intake. Our findings reveal the molecular nature and plasticity of the ME/ARH diffusion barrier, and indicate its physiological role in hypothalamic metabolic hormone sensing.

Zbtb11 interacts with Otx2 and patterns the anterior neuroectoderm in Xenopus.

The zinc finger and BTB domain-containing 11 gene (zbtb11) is expressed in the Xenopus anterior neuroectoderm, but the molecular nature of the Zbtb11 protein during embryonic development remains to be elucidated. Here, we show the role of Zbtb11 in anterior patterning of the neuroectoderm and the cooperative action with the transcription factor Otx2. Both overexpression and knockdown of zbtb11 caused similar phenotypes: expanded expression of the posterior gene gbx2 in the neural plate, and later microcephaly with reduced eyes, suggesting that a proper level of zbtb11 expression is necessary for normal patterning of the neuroectoderm, including eye formation. Co-immunoprecipitation assays showed that Zbtb11 formed a complex with itself and with a phosphomimetic and repressive form of Otx2, suggesting that Zbtb11 forms a dimer or oligomer and interacts with Otx2 in a phosphorylation-dependent manner. Reporter analysis further showed that Zbtb11 enhanced the activity of the phosphomimetic Otx2 to repress a silencer element of the posterior gene meis3. These data suggest that Zbtb11 coordinates with phosphorylated Otx2 to specify the anterior neuroectoderm by repressing posterior genes.

Constraining the low-energy S=−2 meson-baryon interaction with two-particle correlations

In this paper we present a novel method to extract information on hadron-hadron interactions using for the first time femtoscopic data to constrain the low-energy constants of a QCD effective Lagrangian. This method offers a new way to investigate the nonperturbative regime of QCD in sectors where scattering experiments are not feasible, such as the multistrange and charm ones. As an example of its application, we use the very precise K−Λ correlation function data, recently measured in pp collisions at LHC, to constrain the strangeness S=−2 meson-baryon interaction. The model obtained delivers new insights on the molecular nature of the Ξ(1620) and Ξ(1690) states. Published by the American Physical Society 2024

Maternal regulation of the vertebrate oocyte-to-embryo transition.

Maternally-loaded factors in the egg accumulate during oogenesis and are essential for the acquisition of oocyte and egg developmental competence to ensure the production of viable embryos. However, their molecular nature and functional importance remain poorly understood. Here, we present a collection of 9 recessive maternal-effect mutants identified in a zebrafish forward genetic screen that reveal unique molecular insights into the mechanisms controlling the vertebrate oocyte-to-embryo transition. Four genes, over easy, p33bjta, poached and black caviar, were found to control initial steps in yolk globule sizing and protein cleavage during oocyte maturation that act independently of nuclear maturation. The krang, kazukuram, p28tabj, and spotty genes play distinct roles in egg activation, including cortical granule biology, cytoplasmic segregation, the regulation of microtubule organizing center assembly and microtubule nucleation, and establishing the basic body plan. Furthermore, we cloned two of the mutant genes, identifying the over easy gene as a subunit of the Adaptor Protein complex 5, Ap5m1, which implicates it in regulating intracellular trafficking and yolk vesicle formation. The novel maternal protein Krang/Kiaa0513, highly conserved in metazoans, was discovered and linked to the function of cortical granules during egg activation. These mutant genes represent novel genetic entry points to decipher the molecular mechanisms functioning in the oocyte-to-embryo transition, fertility, and human disease. Additionally, our genetic adult screen not only contributes to the existing knowledge in the field but also sets the basis for future investigations. Thus, the identified maternal genes represent key players in the coordination and execution of events prior to fertilization.