Internal Site Research Articles

Enhancement of hydrogen bonds between proteins and polyphenols through magnetic field treatment: Structure, interfacial properties, and emulsifying properties

In food systems, proteins and polyphenols typically coexist in a non-covalent manner. However, the inherent rigid structure of proteins may hinder the binding sites of polyphenols, thereby limiting the strength of their interaction. In the study, magnetic field (MF) treatment was used to enhance non-covalent interactions between coconut globulin (CG) and tannic acid (TA) to improve protein flexibility, enhancing their functional properties without causing oxidation of polyphenols. Based on protein structure results, the interaction between CG and TA caused protein structure to unfold, exposing hydrophobic groups. Treatment with a MF, particularly at 3 mT, further promoted protein unfolding, as evidenced by a decrease in α-helix structure and an increase in coil random. These structural transformations led to the exposure of the internal binding site bound to TA and strengthening the CG-TA interaction (polyphenol binding degree increased from 62.3 to 68.2%). The characterization of molecular forces indicated that MF treatment strengthened hydrogen bonding-dominated non-covalent interactions between CG and TA, leading to improved molecular flexibility of the protein. Specifically, at a MF treatment at 3 mT, CG-TA colloidal particles with small size and high surface hydrophobicity exhibited optimal interfacial activity and wettability (as evidenced by a three-phase contact angle of 89.0°). Consequently, CG-TA-stabilized high internal phase Pickering emulsions (HIPPEs) with uniform droplets and dense gel networks at 3 mT. Furthermore, the utilization of HIPPEs in 3D printing resulted in consistent geometric shapes, uniform surface textures, and distinct printed layers, demonstrating superior printing stability. As a result, MF treatment at 3 mT was identified as the most favorable. This research provides novel insights into how proteins and polyphenols interact, thereby enabling natural proteins to be utilized in a variety of food applications.

Residual Debris within Internal Features of As-received New Dental Implants.

To investigate residual debris within internal features of new 'as received' dental implants. A total of 15 new dental implants representing various dental implant brands were obtained in sealed containers from the manufacturers. Batch numbers and implant types were documented. In a controlled setting, implants were carefully unpacked, and their internal aspects were visually examined. Further analysis involved light microscopy imaging to document and photograph any foreign material. The internal aspect of the implants were sampled with both an endodontic paper cone and a fine bristle brush swab. These were inserted into the implant, rotated three times, then removed and examined under a microscope at 30x magnification. Post sampling some of the brushes/swabs were washed with alcohol to remove debris that could be further examined under magnification. Inspection of the implants without magnification revealed no visible foreign materials. However, under light microscopy (x10 and x30), all 15 implants exhibited small black particles at various internal sites, including connections, threads, and deep within screw channels. Swabs evaluated at magnification detected what appeared to be metal particles in all 15 implants, ranging from distinct metal shards to smaller particles. This study suggests that implant manufacturers have not effectively removed all machining debris from within implant bodies, potentially producing prosthetic and clinical complications.

Simulating the Motion Underlying the Mechanism of Thioredoxin Reductase.

Thioredoxin reductase (TrxR) is an essential antioxidant in most cells; it reduces thioredoxin (Trx) and several more substrates, utilizing NADPH. However, the enzyme's internal active site is too small to accommodate the Trx substrate. Thus, TrxR evolved a disulfide shuttle that can carry reducing equivalents from the active site to the docking site of thioredoxin on the enzyme surface. Yet, in all available atomic structures of TrxR, access to the active site by the shuttle is sterically blocked. We find with computational dynamics that thermal motion at 37 °C allows the oxidized shuttle x to transiently access the active site. Once the shuttle is reduced, it becomes polar. Again, with molecular dynamics, we show that the polar shuttle will move outward toward the solution interface, whereas the oxidized, neutral shuttle will not. This work provides physical evidence for crucial steps in the enzyme mechanism that thus far were just conjectures. The total shuttle motion, from the active site toward the surface, is over 20 Å. TrxR may thus also be termed a molecular machine.

Post-polio syndrome - somatosensory dysfunction and its relation to pain: a pilot study with quantitative sensory testing.

To explore and characterize somatosensory dysfunction in patients with post-polio syndrome and chronic pain, by conducting examinations with Quantitative Sensory Testing. A cross-sectional, descriptive, pilot study conducted during 1 month. Six patients with previously established post-polio syndrome and related chronic pain. All subjects underwent a neurological examination including neuromuscular function, bedside sensory testing, a thorough pain anamnesis, and pain drawing. Screening for neuropathic pain was done with 2 questionnaires. A comprehensive Quantitative Sensory Testing battery was conducted with z-score transformation of obtained data, enabling comparison with published reference values and the creation of sensory profiles, as well as comparison between the study site (more polio affected extremity) and internal control site (less affected extremity) for each patient. Derived sensory profiles showed signs of increased prevalence of sensory aberrations compared with reference values, especially Mechanical Pain Thresholds, with significant deviation from reference data in 5 out of 6 patients. No obvious differences in sensory functions were seen between study sites and internal control sites. Post-polio syndrome may be correlated with a mechanical hyperalgesia/allodynia and might be correlated to a somatosensory dysfunction. With lack of evident side-to-side differences, the possibility of a generalized dysfunction in the somatosensory system might be considered.

The role of defects in high-silica zeolite hydrolysis and framework healing

The stability of high silica zeolites under standard laboratory and mild steaming conditions is understood to be due to the lack of hydrophilic Al-O-Si moieties, which can be targeted by water via hydrolysis reactions with relatively low barriers. However, in hydrophobic high-silica and siliceous frameworks, the specific interactions between water and the internal framework sites are incompletely understood. In particular, the behaviour of common internal defects, including partial hydrolysis species and silanol nests are not established, despite their expected role in accelerating the decomposition of the framework. In this work, we utilise machine learning potentials combined with density functional calculations to rigorously sample the hydrolysis processes in siliceous zeolites with topologies CHA and MFI under low water conditions and quantify the effect of defects. Internal silanol defect sites are found to accelerate zeolite decomposition primarily by bypassing the initial, high-barrier hydrolysis step. Subsequent steps proceed with lower reaction barriers. However, all reaction steps are found to be highly activated, and unlikely to occur rapidly at room temperature under conditions of low internal water concentration. Exchange-healing routes, which reverse hydrolysis while incorporating oxygen from water molecules are found to be competitive along the entire hydrolysis pathway in CHA, providing an additional source of stabilization against hydrolytic decomposition.

2′-O-methylation at internal sites on mRNA promotes mRNA stability

2'-O-methylation (Nm) is a prominent RNA modification well known in noncoding RNAs and more recently also found at many mRNA internal sites. However, their function and base-resolution stoichiometry remain underexplored. Here, we investigate the transcriptome-wide effect of internal site Nm on mRNA stability. Combining nanopore sequencing with our developed machine learning method, NanoNm, we identify thousands of Nm sites on mRNAs with a single-base resolution. We observe a positive effect of FBL-mediated Nm modification on mRNA stability and expression level. Elevated FBL expression in cancer cells is associated with increased expression levels for 2'-O-methylated mRNAs of cancer pathways, implying the role of FBL in post-transcriptional regulation. Lastly, we find that FBL-mediated 2'-O-methylation connects to widespread 3' UTR shortening, a mechanism that globally increases RNA stability. Collectively, we demonstrate that FBL-mediated Nm modifications at mRNA internal sites regulate gene expression by enhancing mRNA stability.

Clovis organizational dynamics at a Late Glacial campsite in the central Great Lakes: Belson site excavations 2020-2021.

The Belson site is located on an outwash plain draining the Early Algonquin stage of the central Great Lakes (coinciding with the Older Dryas stadial period around 14,000 Cal B.P) southwest across Lower Michigan into the Ohio tributaries. By 13,000 Cal B.P the St. Joseph River had incised multiple channels into this plain. On a terrace just north of a now-abandoned channel, a detailed surface study by Talbot from 2005-2018 showed several flake clusters largely of Attica chert, procured about 235 km southwest of Belson. A study of the surface sample was published by the authors in 2021 and indicated that the points were made with the Clovis technological pattern. Excavations in 2020-21 revealed hundreds of buried flakes and multiple tools in the lower, less-disturbed terrace sediment. Plotting of this material indicates successive occupations below the ploughed deposit and covering more than 30 m2. The buried assemblages are similar to the published surface assemblage with the addition of more small scrapers and manufacturing debris. Several of the buried tools have traces of proteins from a range of mammals, suggesting a broad-spectrum subsistence strategy. The documentation of a succession of little disturbed deposits with precisely recorded micro-debris will allow for testing of models describing settlement choice and developing dynamics of internal site organization. Initial analysis of recovered data provides support for an 'outcrop centered' model where high-quality chert outcrops serve as central places on the landscape. Samples of sediment and charcoal for identification and dating await study.

Internal sites of actuation and activation in thin elastic films and membranes of finite thickness.

Functionalized thin elastic films and membranes frequently feature internal sites of net forces or stresses. These are, for instance, active sites of actuation, or rigid inclusions in a strained membrane that induce counterstress upon externally imposed deformations. We theoretically analyze the geometry of isotropic, flat, thin, linearly elastic films or membranes of finite thickness, laterally extended to infinity. At the mathematical core of such characterizations are the fundamental solutions for localized force and stress singularities associated with corresponding Green's functions. We derive such solutions in three dimensions and place them into the context of previous two-dimensional calculations. To this end, we consider both no-slip and stress-free conditions at the top and/or bottom surfaces. We provide an understanding for why the fully free-standing thin elastic membrane leads to diverging solutions in most geometries and compare these situations to the truly two-dimensional case. A no-slip support of at least one of the surfaces stabilizes the solution, which illustrates that the divergences in the fully free-standing case are connected to global deformations. Within the aforementioned framework, our results are important for associated theoretical characterizations of thin elastic films, whether supported or free-standing, and of membranes subject to internal or external forces or stresses.

Structural and Biochemical Characterization of the Nucleosome Containing Variants H3.3 and H2A.Z.

Variant H3.3, along with H2A.Z, is notably enriched at promoter regions and is commonly associated with transcriptional activation. However, the specific molecular mechanisms through which H3.3 influences chromatin dynamics at transcription start sites, and its role in gene regulation, remain elusive. Using a combination of biochemistry and cryo-electron microscopy (cryo-EM), we show that the inclusion of H3.3 alone does not induce discernible changes in nucleosome DNA dynamics. Conversely, the presence of both H3.3 and H2A.Z enhances DNA's flexibility similarly to H2A.Z alone. Interestingly, our findings suggest that the presence of H3.3 in the H2A.Z nucleosome provides slightly increased protection to DNA at internal sites within the nucleosome. These results imply that while H2A.Z at active promoters promotes the formation of more accessible nucleosomes with increased DNA accessibility to facilitate transcription, the simultaneous presence of H3.3 offers an additional mechanism to fine-tune nucleosome accessibility and the chromatin environment.

Steric interaction of iridium sites towards efficient oxygen and hydrogen evolution

Transition metal materials that loaded with trace of Iridium (Ir) are widely accepted as effective catalysts for oxygen evolution (OER) and hydrogen evolution reaction (HER), in which the Ir atoms exposed on the surface can directly affect the electrocatalytic reaction. However, this neglects the Ir – Ir interaction of distinct locations, which may be benefit for the fine-tuning of electronic structure. Herein, we changed the locations (surface and inside) of Ir atoms in the cobalt oxide (Co3O4@NC), and investigated their alkaline OER and HER performances. Combined with X-ray photoelectron spectroscopy (XPS), X-ray absorption spectroscopy (XAS) and theoretical calculations, we infer that the steric interaction induced by the surface – internal Ir sites can weaken the Ir-O bond and optimize the adsorption of intermediates on catalyst surface with a negative shift of d-band center, enabling the surface-Ir sites with lower energy barrier for water dissociation and hydrogen adsorption for HER. Therefore, the as-prepared Irw-Co3O4@NC with surface − inside Ir distribution significantly improve the HER without degrading OER performance, with low overpotential of −173 / −71 mV for HER at −10 mA/cm2 in 0.1 M KOH / 1.0 M KOH, and 244 / 249 mV at 10 mA/cm2 for OER.

Automated Analysis of Split Kidney Function from CT Scans Using Deep Learning and Delta Radiomics.

Background: Differential kidney function assessment is an important part of preoperative evaluation of various urological interventions. It is obtained through dedicated nuclear medical imaging and is not yet implemented through conventional Imaging. Objective: We assess if differential kidney function can be obtained through evaluation of contrast-enhanced computed tomography(CT) using a combination of deep learning and (2D and 3D) radiomic features. Methods: All patients who underwent kidney nuclear scanning at Mayo Clinic sites between 2018-2022 were collected. CT scans of the kidneys were obtained within a 3-month interval before or after the nuclear scans were extracted. Patients who underwent a urological or radiological intervention within this time frame were excluded. A segmentation model was used to segment both kidneys. 2D and 3D radiomics features were extracted and compared between the two kidneys to compute delta radiomics and assess its ability to predict differential kidney function. Performance was reported using receiver operating characteristics, sensitivity, and specificity. Results: Studies from Arizona & Rochester formed our internal dataset (n = 1,159). Studies from Florida were separately processed as an external test set to validate generalizability. We obtained 323 studies from our internal sites and 39 studies from external sites. The best results were obtained by a random forest model trained on 3D delta radiomics features. This model achieved an area under curve (AUC) of 0.85 and 0.81 on internal and external test sets, while specificity and sensitivity were 0.84,0.68 on the internal set, 0.70, and 0.65 on the external set. Conclusion: This proposed automated pipeline can derive important differential kidney function information from contrast-enhanced CT and reduce the need for dedicated nuclear scans for early-stage differential kidney functional assessment. Clinical Impact: We establish a machine learning methodology for assessing differential kidney function from routine CT without the need for expensive and radioactive nuclear medicine scans.

Balanced Mass Transfer and Active Sites Density in Hierarchical Porous Catalytic Metal-Organic Framework for Enhancing Redox Reaction in Lithium-Sulfur Batteries.

Developing highly efficient catalysts, characterized by controllable pore architecture and effective utilization of active sites, is paramount in addressing the shuttle effect and sluggish redox kinetics of lithium polysulfides (LiPSs) in lithium-sulfur batteries (LSBs), which, however, remains a formidable challenge. In this study, a hierarchical porous catalytic metal-organic framework (HPC-MOF) with both appropriate porosity and abundant exposed catalytic sites is achieved through time-controlled precise pore engineering. It is revealed that the evolution of the porous structure and catalytic site density is time-dependent during the etching processes. The moderately etched HPC-MOF-M attains heterogeneous pores at various scales, where large apertures ensure fast mass transfer and micropores inherit high-density catalytic sites, enhancing utilization and catalytic kinetics at internal catalytic sites. Capitalizing on these advantages, LSB incorporating the HPC-MOF-M interlayer demonstrates a 164.6% improvement in discharge capability and an 83.3% lower decay rate over long-term cycling at 1.0C. Even under high sulfur loading of 7.1 mg cm-2 and lean electrolyte conditions, the LSB exhibits stable cycling for over 100 cycles. This work highlights the significance of balancing the relationship between mass transfer and catalytic sites through precise chemical regulation of the porous structure in catalytic MOFs, which are anticipated to inspire the development of advanced catalysts for LSBs.

Constructing Co@C nanoparticles with chainmail-structure for highly efficient hydroformylation of 1-hexene

Constructing highly active noble-metal-free heterogeneous catalysts is the crux for the hydroformylation of long-chain α-olefins. Herein, novel chainmail-structured cobalt oxide nanoparticles (CoO@C|SBA-15) are fabricated by the channel confinement strategy, which display excellent activity for the 1-hexene hydroformylation. Specifically, the obtained catalyst shows 100% 1-hexene conversion and 94% heptanal selectivity, as well as up to 2.0 linear to branch (l/b) ratio, outperforming most of heterogeneous noble metal catalysts. Remarkably, in-situ DRIFT spectra combined with density functional theory calculations disclosed the metallic Co derived from in-situ reconstruction of CoO is the key active site for 1-hexene hydroformylation. Specifically, the reconstructed Co site is responsible for the adsorption of 1-hexene, and the graphite carbon layer promotes the adsorption of H2 and CO by interacting with the reconstructed Co. Moreover, the graphite carbon layer provides a strong protective effect on the internal cobalt active sites and thus enhances the catalytic stability during the harsh condition. This work provides a new method for designing the low-cost heterogeneous catalyst and emphasizes the intrinsic active sites for 1-hexene hydroformylation reaction.

Theoretical prediction of low-energy photoelectron spectra of AlnNi- clusters (n = 1-13).

Mixed-metal clusters have long been studied because of their peculiar properties and how they change with cluster size, composition, and charge state and their potential roles in catalysis. The characterization of these clusters is therefore a very important issue. One of the main experimental tools for characterizing their electronic structure is photoelectron spectroscopy. Theoretical computation completes the task by fully determining the structural properties and matching the theoretical predictions to the measured spectra. We present density functional theory computations of the structural, magnetic, and electronic properties of negatively charged mixed AlnNi- clusters with up to 13 Al atoms. The lowest energy structures of the anionic clusters with up to 7 atoms are also found to be low-energy isomers of the neutral counterparts found in the literature. The 13-atom cluster is found to be a quartet and a perfect icosahedron. The predicted photoelectron spectra are also presented and can be used to interpret future experimental data. We also presented indicators that can be used to determine the potential of these systems for single-atom catalysis. These indicators point to smaller clusters to be more reactive as the gap between the Fermi energy and the center of the d-band increases with cluster size and that Ni occupies an internal site for n = 11-13. We speculate that reactivity can be enhanced if one adds an additional Ni atom. The DFT calculations were performed using the Becke exchange and Perdew-Wang/91 correlation functionals (BPW91), a DFT-optimized all-electron basis set for the aluminum atom, and the Stuttgart small core pseudopotential for the Ni atom. All of the computations used the Gaussian 03 software.

Facile synthesis of amine hybrid silica aerogel globule via wet casting assisted self-catalysed sol-gel process for CO2 capture including direct air capture

Amine hybrid silica aerogel globule (AHSAG) for CO2 capture including direct air capture (DAC) was firstly synthesized via wet casting assisted self-catalyzed sol-gel process. AHSAG has abundant interpenetrating macropores, which favors diffusion of CO2 into internal amine sites and can enhance CO2 adsorption kinetics and capacity. The optimal CO2 adsorption capacity of AHSAG with dry 100% and 400 ppm CO2 are 3.82 (30 °C) and 1.86 mmol/g (55 °C), respectively. Corresponding amine efficiencies are 0.478 and 0.233. The effect of temperature on CO2 adsorption capacity is attributed to simultaneous enhancement of mass transfer kinetics and adsorption thermodynamics. The highest CO2 adsorption rate of AHSAG is achieved at 70 and 55 °C with 100% and 400 ppm CO2, respectively. The trend of CO2 adsorption rate with temperature is attributed to the synergistic effect of diffusion kinetics and desorption. Based on experimental CO2 adsorption kinetics, adsorption mechanism in 400 ppm CO2 was estimated with different diffusion models. Both film diffusion resistance and intraparticle diffusion resistance are involved in CO2 capture of AHSAG from air under given condition to control the overall adsorption process. Three kinetics models were used to fit the experimental data of AHSAG for DAC, and the Avrami model showed the best fitting within the whole adsorption period. Comparing with its state-of-the-art counterparts, AHSAG offers significant advantages for practical DAC, such as high adsorption capacity and amine efficiency, fast adsorption kinetics, and excellent cyclic stability.

Elucidating the role of ferric chloride on carbon capture from low-strength municipal wastewater in high-rate activated sludge process: Parameter optimization and crucial mechanism

To enhance organics capture efficiency from low-strength municipal wastewater of China, FeCl3 enhanced high-rate activated sludge (FC-HRAS) process was established in this work. Effects of sludge concentration and FeCl3 dosage on carbon capture in FC-HRAS were investigated. The optimum sludge concentration of 2.0 g/L and FeCl3 dosage of 30 mg Fe/L were obtained, with total COD removal efficiency of 76.8%. Carbon balance analysis showed that FC-HRAS increased organics capture proportion by 91.8% while reducing loss from oxidative metabolism compared to HRAS. The potential mechanism of enhanced carbon capture for FC-HRAS was further explored. Adding Fe(III) caused coagulation of organics by increasing the Zeta potential in wastewater. Impacted by charge neutralization “compression” and coagulation floc “encirclement”, sludge particle sizes decreased, leading to increases of internal surface area and adsorption site of sludge for binding with bacteria; it facilitated the biological flocculation of FC-HRAS. Meanwhile, Fe(III) binding with proteins in EPS induced formation of “protein shell – β polysaccharides kernel” sludge structure and reduction of sludge negative charge, which intensified sludge stability and agglomeration. These factors explained the increase in organics capture proportion. The decrease in metabolism loss of organics could be attributed to the increase in organics transfer resistance in sludge EPS and selective elimination of heteromorphic bacteria (e.g., denitrifiers) in sludge. This work provided guidance for energy-neutral and cost-saving wastewater treatment in China.

WDR4 promotes HCC pathogenesis through N7-methylguanosine by regulating and interacting with METTL1

BackgroundThe N7-methylguanosine (m7G), a modification at defined internal positions within tRNAs and rRNAs, is correlated with tumor progression. Methyltransferase like 1 (METTL1)/ WD repeat domain 4 (WDR4) mediated tRNA m7G modification, which could alter many oncogenic mRNAs translation to promote progress of multiple cancer types. However, whether and how the internal mRNA m7G modification is involved in tumorigenesis remains unclear. MethodsThe immunohistochemistry assay was conducted to detect the expression of WDR4 and METTL1 in hepatocellular carcinoma (HCC) and the expression of both genes whether contributes to the prognosis of the survival rate of HCC patients. Then, CCK8, colony formation assays and tumor xenograft models were conducted to determine the effects of WDR4 on HCC cells in vitro and vivo. Besides, dot blot assay, m7G-MeRIP-seq and RNA-seq analysis were conducted to determine whether WDR4 contributes to m7G modification and underlying mechanism in HCC cells. Finally, rescue and CO-IP assay were conducted to explore whether WDR4 and METTL1 proteins form a complex in Huh7 cells. ResultsWDR4 modulates m7G modification at the internal sites of tumor-promoting mRNAs by forming the WDR4-METTL1 complex. WDR4 knockdown downregulated the expression of mRNA and protein levels of METTL1 gene and thus further modulate the formation of WDR4-METTL1 complex indirectly. METTL1 expression was markedly correlated with WDR4 expression in HCC tissues. HCC patients with high expression of both genes had a poor prognosis. ConclusionsWDR4 may contribute to HCC pathogenesis by interacting with and regulating the expression of METTL1 to synergistically modulate the m7G modification of target mRNAs in tumor cells.

Very high cycle fatigue of laser powder bed fused Al-Cu-Mg-Ag-TiB2 (A20X) Alloy: Stress relief and aging treatments

This study presents a comprehensive exploration of the fatigue response in the very high cycle fatigue (VHCF) regime for an additively manufactured (i.e., laser powder bed fused) A20X aluminum alloy. Although the need for high-performance materials with exceptional fatigue qualities has increased dramatically, the VHCF behavior of Al-Cu-Mg-Ag-TiB2 (A20X) structures remains largely unknown. A series of ultrasonic fatigue tests were performed to assess the prolonged fatigue life of the A20X alloy (in the VHCF domain where the number of cycles to failure is beyond 10 million cycles). The VHCF response, assessed through ultrasonic fatigue testing, was investigated by examining the stress-life (S-N) curves in a statistical framework, the fatigue crack initiation and propagation behavior, and the fracture surfaces. An asymptotic trend was experimentally found at 109 cycles, with a stress amplitude of 110 MPa for stress-relieved (SR) and 125 MPa for artificially aged (T7) materials, indicating the presence of an endurance limit. Furthermore, fracture surfaces showed the typical fisheye morphology, with a fine granular area (FGA) containing an internal crack-initiating site. The findings of this paper can assist in optimizing fatigue and durability design allowable for applications for extended fatigue life in the VHCF domains.

Aspirin-Mediated Acetylation of SIRT1 Maintains Intestinal Immune Homeostasis.

Aspirin, also named acetylsalicylate, can directly acetylate the side-chain of lysine in protein, which leads to the possibility of unexplained drug effects. Here, the study used isotopic-labeling aspirin-d3 with mass spectrometry analysis to discover that aspirin directly acetylates 10 HDACs proteins, including SIRT1, the most studied NAD+-dependent deacetylase. SIRT1 is also acetylated by aspirin in vitro. It is also identified that aspirin directly acetylates lysine 408 of SIRT1, which abolishes SIRT1 deacetylation activity by impairing the substrates binding affinity. Interestingly, the lysine 408 of SIRT1 can be acetylated by CBP acetyltransferase in cells without aspirin supplement. Aspirin can inhibit SIRT1 to increase the levels of acetylated p53 and promote p53-dependent apoptosis. Moreover, the knock-in mice of the acetylation-mimic mutant of SIRT1 show the decreased production of pro-inflammatory cytokines and maintain intestinal immune homeostasis. The study indicates the importance of the acetylated internal functional site of SIRT1 in maintaining intestinal immune homeostasis.

Hierarchical core-shell structured CoZn-MOFs derived materials anode with raspberry-like shape for high-performance lithium storage

Significant progress had been made in various fields with transition metal oxide electrode materials, particularly in battery materials where structural control played a crucial role in enhancing their electrochemical properties. Therefore, this study aimed to investigate the potential of a raspberry-like hierarchical core-shell structure derived from Co–Zn MOF as anode materials by varying concentration of reaction solution in hydrothermal method. The hierarchical raspberry-like hollow shell structure was beneficial to expose more active sites and reduced the diffusion distance of Li+ to the internal electroactive sites, improving the overall electrical conductivity of the electrode by full contact with carbon. Carbon nanotubes were incorporated into more suitable core-shell structure. They were uniformly coated the hollow sphere and filled inside of that to form a carbon skeleton. Specifically, the carbon nanotubes inside of the hollow sphere supported the shell not to collapse. This mitigated volume expansion during the cycling process, maintains structure stability, and allowed for rearrangement to occur during cycling to achieve a high specific capacity. Furthermore, the carbon nanotubes inside and outside of the hollow sphere created a high-density interface that enhanced interfacial polarisation and accelerated the rate of Li+ passage during cycling. These effects had resulted in an improvement in the material's performance. It is noteworthy that the specific capacity attains 1050 mAh g-1 when exposed to a current density of 0.2 A g-1. Notably, even after conducting 500 cycles at a current density of 0.5 A g-1, the specific capacity remains stable at 652 mAh g-1.