Distinct Properties Research Articles

Abstract B012: TP53 missense mutations and keratin 17 are negative prognostic biomarkers in pancreatic ductal adenocarcinoma

Abstract Background: Cancer patients with similar clinical and pathologic characteristics may have different responses to treatments and survival, which may be attributable to distinct molecular properties of their tumors. In pancreatic ductal adenocarcinomas (PDACs), there is a pressing need to identify prognostic biomarkers that could help us to predict disease progression and patient survival. Our group previously reported that keratin17 (K17) expression is a hallmark of PDACs of patients with the shortest patient survival. Furthermore, there is some evidence suggesting that missense mutations in TP53 are associated with worse survival in patients with PDAC. To date, however, no studies have addressed the differential prognostic value of molecular characterization of TP53 coupled with K17 expression for predicting survival in patients with PDAC. Objective and methods: To fill this gap, we assessed the effect of different TP53 mutations and K17 expression on patient survival, using a clinically annotated cohort of 128 patients containing molecular profiling on patient tumors. K17 Immunohistochemistry (IHC) staining on patient’s formalin-fixed, paraffin-embedded (FFPE) tissue blocks were performed to assess the expression of this marker in tumor cells. K17 IHC scoring was conducted based on a subjective assessment of the overall proportion of stained cells relative to the overall number of tumor cells present in a single representative section from each case. Kaplan-Meier and Cox proportional hazards regression models were analyzed to determine survival differences of patients with PDACs harboring different TP53 mutations and levels of K17 IHC expression, adjusting for patient demographics (age at diagnosis, sex, race/ethnicity) and tumor characteristics (presence of distant metastasis at diagnosis). Results: Tumors were classified as high for K17 when ≥90% of tumor cells showed strong staining. High-K17 cases (n=16;12.50%) had shorter survival compared with low-K17 cases (n=112; 87.50%) (26.80 vs. 16.77 months; P=0.035). The majority of cases harbored missense mutations in TP53 (42.19%), while about one-third harbored truncating TP53 (27.34%) mutations. We found that PDACs with missense TP53 mutations and high K17 were associated with worse patient survival compared to tumors with missense TP53 and low K17 expression (HR=5.27; 95% CI, 1.76-15.82; P=0.003). Similarly, compared with patients with wild-type TP53 and low K17, patients with both missense TP53 mutations and high K17 had significantly worse survival (HR=3.51, 95% CI, 1.45-8.51; P=0.005). Conclusions: Our findings suggest that molecular characterization of specific TP53 mutations coupled with K17 IHC staining may help to determine differences in patient prognosis and identify subgroups with worse patient survival, therefore, potentially guiding future clinical management of patients. Citation Format: Carlos Mauricio Mejia Arbelaez, Gabriella Baraks, Lyanne Oblein, Michael Horowitz, Lynn Matrisian, Kenneth Shroyer, Luisa Fernanda Escobar-Hoyos. TP53 missense mutations and keratin 17 are negative prognostic biomarkers in pancreatic ductal adenocarcinoma [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Pancreatic Cancer; 2023 Sep 27-30; Boston, Massachusetts. Philadelphia (PA): AACR; Cancer Res 2024;84(2 Suppl):Abstract nr B012.

Stability and Electronic Properties of Mixed Rare-Earth Tri-Metallofullerenes YxDy3-x@C80 (x = 1 or 2).

Tri-metallofullerenes, specifically M3@C80 where M denotes rare-earth metal elements, are molecules that possess intriguing magnetic properties. Typically, only one metal element is involved in a given tri-metallofullerene molecule. However, mixed tri-metallofullerenes, denoted as M1xM23-x@C80 (x = 1 or 2, M1 and M2 denote different metal elements), have not been previously discovered. The investigation of such mixed tri-metallofullerenes is of interest due to the potential introduction of distinct properties resulting from the interaction between different metal atoms. This paper presents the preparation and theoretical analysis of mixed rare-earth tri-metallofullerenes, specifically YxDy3-x@C80 (x = 1 or 2). Through chemical oxidation of the arc-discharge produced soot, the formation of tri-metallofullerene cations, namely Y2Dy@C80+ and YDy2@C80+, has been observed. Density functional theory (DFT) calculations have revealed that the tri-metallofullerenes YxDy3-x@C80 (x = 1 or 2) exhibit a low oxidation potential, significantly lower than other fullerenes such as C60 and C70. This low oxidation potential can be attributed to the relatively high energy level of a singly occupied orbital. Additionally, the oxidized species demonstrate a large HOMO-LUMO gap similar to that of YxDy3-xN@C80, underscoring their high chemical stability. Theoretical investigations have uncovered the presence of a three-center two-electron metal-metal bond at the center of Y2DY@C80+ and YDy2@C80+. This unique multi-center bond assists in alleviating the electrostatic repulsion between the metal ions, thereby contributing to the overall stability of the cations. These mixed rare-earth tri-metallofullerenes hold promise as potential candidates for single-molecule magnets.

Sulfonylurea receptor 2 (SUR2), intricate sensors for intracellular Mg-nucleotides.

SUR2, similar to SUR1, is a regulatory subunit of the ATP-sensitive potassium channel (KATP), which plays a key role in numerous important physiological processes and is implicated in various diseases. Recent structural studies have revealed that, like SUR1, SUR2 can undergo ligand-dependent dynamic conformational changes, transitioning between an inhibitory inward-facing conformation and an activating occluded conformation. In addition, SUR2 possesses a unique inhibitory Regulatory helix (R helix) that is absent in SUR1. The binding of the activating Mg-ADP to NBD2 of SUR2 competes with the inhibitory Mg-ATP, thereby promoting the release of the R helix and initiating the activation process. Moreover, the signal generated by Mg-ADP binding to NBD2 might be directly transmitted to the TMD of SUR2, prior to NBD dimerization. Furthermore, the C-terminal 42 residues (C42) of SUR2 might allosterically regulate the kinetics of Mg-nucleotide binding on NBD2. These distinctive properties render SUR2 intricate sensors for intracellular Mg-nucleotides.

Topological star junctions: Linear modes and solitons

We address continuous two-dimensional (2D) star-junctions formed by different numbers of Su–Schrieffer-Heeger (SSH) chains that have one common waveguide in the center of the junction. We show that by changing waveguide shifts in the dimers forming individual SSH chains, one can create a rich variety of modes in the center of the junction. Independently of the relation between non-equal bonds of the SSH chains, the in-gap modes localized in the center of the junction can be considered as topological, either representing extensions of the conventional topological edge stages or being modes induced by a defect at one of the SSH chain edges. Degeneracy of the eigenvalues and structure of the localized modes of fully 2D junctions depend on their symmetry and number of chains, and are different from their 1D counterparts obtained in the tight-binding approximation. In the presence of the focusing nonlinearity of the medium such states give rise to families of solitons with distinct stability properties depending on the number of chains in junction, waveguide shifts, and mode symmetry.

Mechanical Manipulation of Quantum Interference in Single-Molecule Junctions.

Mechanosensitive molecular junctions, where conductance is sensitive to an applied stress such as force or displacement, are a class of nanoelectromechanical systems unique for their ability to exploit quantum mechanical phenomena. Most studies so far relied on reconfiguration of the molecule-electrode interface to impart mechanosensitivity, but this approach is limited and, generally, poorly reproducible. Alternatively, devices that exploit conformational flexibility of molecular wires have been recently proposed. The mechanosensitive properties of molecular wires containing the 1,1'-dinaphthyl moiety are presented here. Rotation along the chemical bond between the two naphthyl units is possible, giving rise to two conformers (transoid and cisoid) that have distinctive transport properties. When assembled as single-molecule junctions, it is possible to mechanically trigger the transoid to cisoid transition, resulting in an exquisitely sensitive mechanical switch with high switching ratio (> 102). Theoretical modeling shows that charge reconfiguration upon transoid to cisoid transition is responsible for the observed behavior, with generation and subsequent lifting of quantum interference features. These findings expand the experimental toolbox of molecular electronics with a novel chemical structure with outstanding electromechanical properties, further demonstrating the importance of subtle changes in charge delocalization on the transport properties of single-molecule devices.

Sensory signature of lignins, new generation of bio-based ingredients in cosmetics

Lignins represent a high interest in cosmetics as promising multifunctional ingredients. Despite this, uncovering the sensory profile of lignin-based emulsions has remained an unexplored frontier. This study aims to bridge this gap by employing expert sensory evaluation and instrumental characterization to assess the sensory attributes of lignin-based emulsions. A comparative analysis with commercial tinted products and discrimination among lignin derivatives were integral components of the research. Results underscored the distinctive sensory properties of lignin emulsions, exhibiting significantly higher “Integrity of shape” (7.0 ± 0.1) compared to commercial products (4.8 ± 0.1). Additionally, lignin emulsions displayed longer play-time until skin absorption (4.3 ± 0.1), contrasting with the quicker absorption of commercial products (2.7 ± 0.4) and their shorter play-time. Depending on application requirements, lignin derivatives offer formulators a versatile sensory toolbox. Discrimination of lignin emulsions on certain texture properties was achieved using various instrumental tools. Despite the complex formulation of commercial products compared to lignin emulsions, similar texture properties were observed, showcasing lignins' potential to replace multiple ingredients in tinted cosmetics. Beyond their established antioxidant, anti-UV, anti-bacterial, and emulsifying properties, this study reveals additional advantageous sensory properties of lignins, positioning them as promising plant-based sensory ingredients in sustainable cosmetic applications.

Quenching of G4-DNA intrinsic fluorescence by ligands.

G-quadruplex (G4) structures formed by the guanine-rich DNA regions exhibit several distinctive optical properties, including UV absorption and circular dichroism spectra. Some G4 DNA possess intrinsic UV fluorescence whose origin is not completely clear to date. In this work, we study the effect of TMPyP4 and Methylene Blue on the intrinsic fluorescence of the dimeric G4 DNA structure formed by two d(G3T)4 sequences. We demonstrate that binding of the ligands results in quenching of the intrinsic fluorescence, although the conformation of the G4 DNA and its dimeric structure remain preserved. The binding sites of the ligands were suggested by the photoinduced oxidation of guanines and analysis of binding isoterms. We discuss how DNA-ligand complexes can affect the intrinsic fluorescence of G4 DNA.

Suction and anisotropy effects on the stiffness characteristics of a compacted lateritic clay from small to large strains

Lateritic clay has distinct properties from other clays due to its high sesquioxide content. Its stiffness characteristics have not been well understood, especially when the soil is unsaturated and anisotropic. This study investigated the stiffness characteristics of compacted lateritic clay through suction-controlled triaxial compression tests equipped with local strain measurements. Both vertically and horizontally cut specimens were tested to determine the evolution of stiffness anisotropy during shearing. Three suctions (0, 10, and 150 kPa) and two confining pressures (50 and 200 kPa) were considered. When strains are relatively small (e.g., less than 0.2%), the secant Young's modulus Esec of vertical specimens is consistently higher than that of horizontal specimens at all suctions and stresses due to the inherent anisotropic structure. The degree of anisotropy increases with increasing suction since suction enhances the stiffness more significantly in vertical specimens than in horizontal specimens. This behaviour may be due to an enhanced force chain in the vertical direction during shearing. As strains increase, the degradation of Esec normalized by the maximum Young's modulus E0 is almost independent of suction and anisotropy. Lateritic clay has a higher degradation rate than other clays with a similar plasticity index because of its aggregated microstructure.

Multi-phase retrieval of methane hydrate in natural sediments by cryogenic x-ray computed tomography.

In this study, we observed natural methane (CH4) hydrate sediments, which are a type of unconventional natural gas resources, using x-ray computed tomography (CT). Because CH4 hydrates are formed by hydrogen bonding of water molecules with CH4, material decomposition becomes challenging when CH4 hydrates coexist with liquid or solid water in natural sediments. Tri-contrast (absorption, refraction, and scattering) imaging was performed via diffraction enhanced x-ray CT optics using monochromatic synchrotron x rays. The quantitative characterization of the contrast changes successfully enabled the decomposition of CH4 hydrates coexisting with frozen seawater (ice) in natural sediments obtained from the Okhotsk Sea. This study reveals complementary structural information about the microtexture and spatial relation among CH4 hydrates, ice, and pores by utilizing the distinct physical properties of x rays when passing through the materials. These results highlight the exceptional capabilities of high-resolution multicontrast x-ray tomography in materials science and geoscience applications.

Biosensing Applications of Molecularly Imprinted-Polymer-Based Nanomaterials

In the realm of sensing technologies, the appeal of sensors lies in their exceptional detection ability, high selectivity, sensitivity, cost-effectiveness, and minimal sample usage. Notably, molecularly imprinted polymer (MIP)-based sensors have emerged as focal points of interest spanning from clinical to environmental applications. These sensors offer a promising avenue for rapid, selective, reusable, and real-time screening of diverse molecules. The preparation technologies employed in crafting various polymer formats, ranging from microparticles to nanomaterials, wield a profound influence. These techniques significantly impact the assembly of simplified sensing systems, showcasing remarkable compatibility with other technologies. Moreover, they are poised to play a pivotal role in the realization of next-generation platforms, streamlining the fabrication of sensing systems tailored for diverse objectives. This review serves as a comprehensive exploration, offering concise insights into sensors, the molecular imprinting method, and the burgeoning domain of MIP-based sensors along with their applications. Delving into recent progress, this review provides a detailed summary of advances in imprinted-particle- and gel-based sensors, illuminating the creation of novel sensing systems. Additionally, a thorough examination of the distinctive properties of various types of MIP-based sensors across different applications enriches the understanding of their versatility. In the concluding sections, this review highlights the most recent experiments from cutting-edge studies on MIP-based sensors targeting various molecules. By encapsulating the current state of research, this review acts as a valuable resource, offering a snapshot of the dynamic landscape of MIP-based sensor development and its potential impact on diverse scientific and technological domains.

Survey of Main Group Metals and Metalloids in Cancer Treatment

Cancer is one of the leading causes of human death among all major diseases. Metal-based complexes are considered as the most promising vital part in the existing arsenal of cytotoxic candidates used in cancer therapy and diagnostics. The efforts of many scientific groups resulted in the development of numerous metal-based compounds featuring different biologically active organic ligands in order to modulate their bioactivity. Along with the main representatives as potential therapeutic agents, such as the complexes Pt(II)/Pt(IV), Pd(II), Ru(II)/Ru(III), Ag(I), Au(I)/Au(III), Ti(IV), V(IV) and Ga(III), many other transition metal and lanthanide complexes possessing antiproliferative activity are widely discussed in the literature. However, such drugs remain outside the scope of this review. The main purpose of the current study is to review the potential activity of main group metal- and metalloid-based complexes against the most common cancer cell types, such as carcinomas (lung, liver, breast, kidney, gastric, colorectal, bladder, ovarian, cervical, prostate, etc.); sarcomas; blastomas; lymphomas; multiple myeloma; and melanoma. Overcoming the long disregard of organometallic compounds of metals and metalloids from the main groups, a growing number of emerging anticancer agents remarkably prove this field offers an extensive variety of new options for the design of innovative unexplored chemopharmaceutics. Moreover, some of the metal complexes and organometallic compounds from these elements can exhibit entirely different, specific modes of action and biological targets. Obviously, exploitation of their distinct properties deserves more attention.

Light-front puzzles

Light-front formulations of quantum field theories have many advantages for computing electroweak matrix elements of strongly interacting systems and other quantities that are used to study hadronic structure. The theory can be formulated in Hamiltonian form so non-perturbative calculations of the strongly interacting initial and final states are in principle reduced to linear algebra. These states are needed for calculating parton distribution functions and other types of distribution amplitudes that are used to understand the structure of hadrons. Light-front boosts are kinematic transformations so the strongly interacting states can be computed in any frame. This is useful for computing current matrix elements involving electroweak probes where the initial and final hadronic states are in different frames related by the momentum transferred by the probe. Finally in many calculations the vacuum is trivial so the calculations can be formulated in Fock space. The advantages of light front-field theory would not be interesting if the light-front formulation was not equivalent to the covariant or canonical formulations of quantum field theory. Many of the distinguishing properties of light-front quantum field theory are difficult to reconcile with canonical or covariant formulations of quantum field theory. This paper discusses the resolution of some of the apparent inconsistencies in canonical, covariant and light-front formulations of quantum field theory. The puzzles that will be discussed are (1) the problem of inequivalent representations (2) the problem of the trivial vacuum (3) the problem of ill-posed initial value problems (4) the problem of rotational covariance (5) the problem of zero modes and (6) the problem of spontaneously broken symmetries.

Review of electrocatalytic reduction of CO2 on carbon supported films

Carbon capture and conversion are becoming increasingly important as atmospheric CO2 concentrations rise and their adverse effects become increasingly evident. CO2 conversion/utilization-related research has gained renewed interest on a variety of platforms, including thermal, solar, biological, photochemical, and electrochemical conversions. Electrochemical routes, using suitable catalysts, are potentially suitable for commercial purposes owing to ease of integration with solvent-based carbon capture processes. This paper summarizes and evaluates the studies conducted within the past decade regarding the feasibility of carbon-based supports utilized in electrocatalytic carbon dioxide reduction. CO2 conversion has been reviewed in a number of reports, focusing on specific sections, such as metallic/bimetallic catalysts, CO2 solubility, and the fabrication of electrodes and electrochemical cells. The number of publications addressing various carbon-based electrocatalysts is increasing, but these materials have not yet been reviewed. Herein, we are focused on three types of electrocatalyst materials: metals, metal-oxides, non-oxides, and combinations thereof with carbon. The scope of this study includes the following: i) carbon-based materials and how they are characterized by distinctive properties, ii) electrocatalytic CO2 conversion techniques, and iii) research cases for carbon allotrope-supported composites used in CO2 reduction. The advancement in analytical tools that provide insight into liquid-phase reactions will benefit the development of catalysts and electrodes that will be effective in converting CO2 into the desired products. Such developments will also be applicable to other systems involving liquid electrolytes or solvents for performing reactions on catalyst surfaces.

Biochemical, Biophysical, and Structural Analysis of an Unusual DyP from the Extremophile Deinococcus radiodurans.

Dye-decolorizing peroxidases (DyPs) are heme proteins with distinct structural properties and substrate specificities compared to classical peroxidases. Here, we demonstrate that DyP from the extremely radiation-resistant bacterium Deinococcus radiodurans is, like some other homologues, inactive at physiological pH. Resonance Raman (RR) spectroscopy confirms that the heme is in a six-coordinated-low-spin (6cLS) state at pH 7.5 and is thus unable to bind hydrogen peroxide. At pH 4.0, the RR spectra of the enzyme reveal the co-existence of high-spin and low-spin heme states, which corroborates catalytic activity towards H2O2 detected at lower pH. A sequence alignment with other DyPs reveals that DrDyP possesses a Methionine residue in position five in the highly conserved GXXDG motif. To analyze whether the presence of the Methionine is responsible for the lack of activity at high pH, this residue is substituted with a Glycine. UV-vis and RR spectroscopies reveal that the resulting DrDyPM190G is also in a 6cLS spin state at pH 7.5, and thus the Methionine does not affect the activity of the protein. The crystal structures of DrDyP and DrDyPM190G, determined to 2.20 and 1.53 Å resolution, respectively, nevertheless reveal interesting insights. The high-resolution structure of DrDyPM190G, obtained at pH 8.5, shows that one hydroxyl group and one water molecule are within hydrogen bonding distance to the heme and the catalytic Asparagine and Arginine. This strong ligand most likely prevents the binding of the H2O2 substrate, reinforcing questions about physiological substrates of this and other DyPs, and about the possible events that can trigger the removal of the hydroxyl group conferring catalytic activity to DrDyP.

Structure and Function of Auxin Transporters.

Auxins, a group of central hormones in plant growth and development, are transported by a diverse range of transporters with distinct biochemical and structural properties. This review summarizes the current knowledge on all known auxin transporters with respect to their biochemical and biophysical properties and the methods used to characterize them. In particular, we focus on the recent advances that were made concerning the PIN-FORMED family of auxin exporters. Insights derived from solving their structures have improved our understanding of the auxin export process, and we discuss the current state of the art on PIN-mediated auxin transport, including the use of biophysical methods to examine their properties. Understanding the mechanisms of auxin transport is crucial for understanding plant growth and development, as well as for the development of more effective strategies for crop production and plant biotechnology.

Additive manufacturing of multi-materials with interfacial component gradient by in-situ powder mixing and laser powder bed fusion

Defects (e.g., pores and cracks) and high stress concentration derived from the significant mutation in materials are the critical challenge for multi-material structures fabricated by laser powder bed fusion (LPBF). Introducing a transition zone between dissimilar materials with a composition gradient at the interface may be a promising approach to resolve or minimize these problems. In this work, three distinct CuSn10 copper alloy (CuA)/316 L stainless steel (SS) multi-material gradient structures (i.e., CS, SC-1, and SC-2) were fabricated by a LPBF system with in-situ powder mixing and feeding capability. A buffer layer material based on the mixture of the two base materials was introduced at the interface between CuA and SS. The effects of the building strategies and interfacial composition gradient transition paths on the interfacial bonding characteristics were investigated. The microstructure evolution and the underlying interfacial bonding mechanisms were discussed. It was found that the interfacial bonding behaviors were critically dependent on the occurrence of liquid metal embrittlement induced by Cu penetration into Fe grains, as well as the width and microstructure gradient of the diffusion zone and high stress concentration at the interface. A non-uniform melting behavior of CuA and SS powders could be induced by the distinct thermal-physical properties between the two materials, which could lead to lack-of-fusion pores at the interface. In the CS sample, printing SS on the CuA with a buffer layer material could inhibit the formation of Cu-penetration cracks and increase the width of the diffusion zone, which may enhance the interfacial metallurgical bonding. This work may enhance the essential comprehension of improving interfacial bonding strength of LPBF-processed multi-material structures.

Pore-Networked Soft Materials Based on Metal-Organic Polyhedra.

ConspectusThe last two decades have witnessed a tremendous development of crystalline microporous adsorbents in a wide range of applications including molecular adsorption, storage and separation, purification, as well as catalysis. The main players as porous materials that have contributed to the developments are extended molecular frameworks (e.g., metal-organic frameworks, MOFs; covalent-organic frameworks, COFs) or discrete porous molecules (e.g., metal-organic cages, MOCs; porous organic cages, POCs) thanks to the high degrees of freedom in their structural designability and tunability. To overcome the processability issue originating from their powder forms after synthesis, one main strategy is to hybridize the microporous adsorbents as pore-containing fillers with solvents or polymers as processable matrices to produce porous soft materials, such as porous liquids, gels/aerogels, and mixed-matrix membranes, depending on the form of matrix used. Nevertheless, the fabrication of "ideal" hybrid materials relies on the homogeneous distribution of the pore-containing fillers within the matrices. It is still challenging to find a versatile way to solve the aggregation issues of fillers and their insufficient interaction with the matrices, which are concerned with inhibiting the translation of the distinctive properties of microporous adsorbents into the obtained hybrid soft materials.Herein, we describe a new bottom-up approach for the fabrication of "pore-networked soft materials" based on the concept of directly interconnecting the pore-containing fillers into a continuous pore network within the matrices. The advantages of the pore-networking strategy lie in two main aspects: (i) the elimination of the need to struggle with the aggregation issue of fillers due to their overall interconnection throughout the matrices; (ii) the generation of continuous pore networks that guarantee the efficient molecular mass transfer in the materials. In this Account, we summarize our state-of-the-art progress of pore-networked soft materials based on the use of MOCs, alternatively called metal-organic polyhedra (MOPs) herein, as pore units for the pore network construction. The good solubility of MOPs in organic solvents allows them to be feasibly processed in solution, wherein the coordination of MOPs with organic linkers leads to the formation of linked MOP gels featuring not only intrinsic MOP cavities but also tunable extrinsic porosities generated between linked MOPs through the control of MOP/linker structures and network connectivity. Furthermore, the matrix of the linked MOP network, here referred to as the continuous phase with respect to the entire porous MOP network, is not limited to the solvents. We anticipate that the implementation of air, liquids, and polymers as the matrices could result in different forms of pore-networked soft materials like aerogels, foams, gels, monoliths, and membranes. For instance, we demonstrate the fabrication of linked MOP aerogel and permanently porous gel with their potential applications on selective CO2 photoreduction and gas sorption, respectively. We believe that the pore-network strategies will advance the development of porous soft materials featuring unique advantages and properties beyond the current hybrid systems.

Integrated untargeted metabolomic and transcriptomic analyses reveal OMT genes controlling polymethoxyflavonoid biosynthesis in the pericarp of Citrus reticulata ‘Chachi’

The dried pericarp of Citrus reticulata 'Chachi' (CRC) is commonly utilized in Traditional Chinese Medicine (TCM) and food consumption. Geqingpi (GQP), Sihuaqingpi (SHQP) and Guangchenpi (CRP) are TCM materials derived from different developmental stages of CRC pericarp, each possessing distinct medicinal properties. However, there is currently limited study on the active substances in these three stages. Metabolome data suggested that the discrepancies in flavonoid content, particularly polymethoxyflavonoids (PMFs), predominantly contribute to the variations across the three periods. Additionally, through multivariate statistical analysis, 7 potential biomarkers were identified and nobiletin (NOB) possessed the most significant contribution. O-methyltransferases (OMTs) play a crucial role to catalyze the formation of -OCH3 in PMFs. The analysis of transcriptome and genome data revealed the presence of 93 CrOMTs in CRC and 43 were expressed on pericarp. Further investigation identified that 28 of these genes were potentially responsible for catalyzing the biosynthesis of important PMFs such as NOB, sinensetin (SIN), and 3,3′,4′,5,6,7,8-heptamethoxyflavone (HEP). Our results may provide a new perspective for the study of GQP, SHQP and CRP, as well as the regulatory mechanism of PMFs in CRC.

Panoply of Ni-Doping-Induced Reconstructions, Electronic Phases, and Ferroelectricity in 1T-MoS2.

The distorted phases of monolayer 1T-MoS2 have distinct electronic properties, with potential applications in optoelectronics, catalysis, and batteries. We theoretically investigate the use of Ni-doping to generate distorted 1T phases and find not only the ones usually reported but also two further phases (3 × 3 and 4 × 4), depending on the concentration and the substitutional or adatom doping site. Corresponding pristine phases are stable after removal of dopants, which might offer a potential route to experimental synthesis. We find large ferroelectric polarizations, most notably in 3 × 3 which─compared to the recently measured 1T″─has 100 times greater ferroelectric polarization, a lower energy, and a larger band gap. Doped phases include exotic multiferroic semimetals, ferromagnetic polar metals, and improper ferroelectrics with only in-plane polarization switchable. The pristine phases have unusual multiple gaps in the conduction bands with possible applications for intermediate band solar cells, transparent conductors, and nonlinear optics.

A mechanically durable slippery liquid-infused porous surface based on distinctive ‘jaboticaba-like’ TiO2/sepiolite nanocomposites with superior hot water repellency and anti-corrosion for protecting various substrates

Slippery liquid infused porous surfaces (SLIPS) are widely utilized due to their omniphobicity and distinctive slippery properties. Fragile mechanical properties and unstable lubricant layer of SLIPS have a substantial impact on its long-term application performance. Herein, a pre-oil-infused mechanically robust organic/inorganic composite superhydrophobic surface (SC) for SLIPS with hierarchical roughness was obtained by in-situ growing a significant amount TiO2 nanospheres on the surface of sepiolite (SEP) fiber structures via hydrogen bonding, Ti-O-Si covalent bonding, and electrostatic power, resulting in a unique bionic “jaboticaba-like” structure on SC. Through hydrogen bonding, the hydroxyl groups on the TiO2 surface can also interact with the cross-linked polymer PVDF-HFP (polyethylene fluoride hexafluoropropylene). In the presence of multiple interactions, SC could resist 300 cycles of a rigorous Taber rubbing test with a 500 g weight and yet retain superhydrophobicity. The prepared SLIPS have exceptional hot water (boiling water) resistance, strong shear stability (8000 rpm/min), and water jetting resistance (40 kPa). Corrosion current density of SLIPS and SC was decreased by roughly 4 orders of magnitude and 3 orders of magnitude, respectively, after exposure to 3.5 wt% NaCl solution as compared to bare aluminum substrate. SLIPS have higher long-term corrosion resistance compared to SC. Owing to the “jaboticaba-like” hierarchical structure, SLIPS have great oil-locking capabilities, as well as good mechanical stability and long-term corrosion resistance. This article offers recommendations for developing tough SLIPS for future engineering applications.