Publications by authors named "Shie J"

This study investigated the feasibility of using/reusing commercial activated carbon (CAC) for the capture of high molecular weight and high-boiling point volatile organic compounds (HBPVOCs). The CAC was first characterized using proximate analysis, heat value analysis, iodine value analysis, element analysis, inductively coupled plasma spectrometry, and specific surface area analysis. We then assessed the adsorption/desorption performance of a CAC-based PSA system for the removal of Butyl Cellosolve (BCS), a HBPVOC commonly used in paints, coatings, cleaners, and industrial processes.

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  • The study investigated exopolysaccharides from the bacterium Clostridium ventriculi, which were previously thought to be mainly cellulose, but were found to contain (1,3;1,4)-β-D-glucans.
  • Researchers used the enzyme lichenase to break down these exopolysaccharides, confirming the presence of (1,3;1,4)-β-D-glucans rather than cellulose.
  • Genomic analysis identified two glycosyltransferase genes (CvGT2-1 and CvGT2-2) that were shown to encode enzymes responsible for synthesizing (1,3;1,4)-β-D-glucans in yeast experiments.
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Eukaryotic ribosomal proteins contain extended regions essential for translation coordination. Dedicated chaperones stabilize the associated ribosomal proteins. We identified Bcp1 as the chaperone of uL14 in Saccharomyces cerevisiae.

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The assembly and disassembly of biomolecular condensates are crucial for the subcellular compartmentalization of biomolecules in the control of cellular reactions. Recently, a correlation has been discovered between the phase transition of condensates and their maturation (aggregation) process in diseases. Therefore, modulating the phase of condensates to unravel the roles of condensation has become a matter of interest.

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  • Eliminating core fucose from Fc antibody glycoforms can increase the efficacy of therapeutic antibodies, particularly enhancing ADCC, but traditional fucosidases have limitations in effectiveness.
  • A newly identified α-l-fucosidase (fucA) from a bacterium shows high reactivity to specific fucose linkages while demonstrating robust stability and activity under various conditions.
  • Using fucA in glycoengineering of the antibody adalimumab achieved efficient removal of core fucose, leading to a more effective afucosylated form with improved binding to Fcγ receptor IIIa.
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This study explored visual perception skills and the ability to write according to standard stroke order and their links to the learning of Chinese handwriting. Thirty-seven children (aged 6-8) (15 boys and 22 girls) participated in a handwriting test and visual perception evaluation (Test of Visual Perceptual Skills-3rd Edition, TVPS-3). A computerized system was used to evaluate the stroke order accuracy, legibility, and automation of stroke movements.

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  • Hirudins are natural proteins that serve as anticoagulants by directly blocking thrombin, an important factor in blood coagulation.
  • They mainly inhibit thrombin through interactions at both its active and regulatory sites, with sulfate groups on certain amino acids enhancing their binding.
  • Research on synthesized hirudin peptides showed that adding sulfotyrosine or more negatively charged amino acids didn't significantly improve thrombin inhibition, even though one peptide showed better binding to thrombin.
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Multicolor labeling for monitoring the intracellular localization of the same target type in the native environment using chemical fluorescent dyes is a challenging task. This approach requires both bioorthogonal and biocompatible ligations with an excellent fluorescence signal-to-noise ratio. Here, we present a metabolic glycan labeling technique that uses homemade fluorogenic dyes to investigate glycosylation patterns in live cells.

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The carnivorous mushroom uses an unknown toxin to rapidly paralyze and kill nematode prey upon contact. We report that small lollipop-shaped structures (toxocysts) on fungal hyphae are nematicidal and that a volatile ketone, 3-octanone, is detected in these fragile toxocysts. Treatment of with 3-octanone recapitulates the rapid paralysis, calcium influx, and neuronal cell death arising from fungal contact.

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Background: Pregnenolone (P5) is a neurosteroid that promotes microtubule polymerization. It also reduces stress and negative symptoms of schizophrenia, promotes memory, as well as recovery from spinal cord injury. P5 is the first substance in the steroid-synthetic pathway; it can be further metabolized into other steroids.

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Polygonatum odoratum is a perennial rhizomatous medicinal plant and different plant parts have been used in the treatment of various ailments. Herein, we have investigated the structural compositions of rhizome, leaf, and stem cell walls. We found 30-44% of polysaccharides in these wall preparations were cyclohexanediaminetetraacetic acid (CDTA) extractable, the proportion of heteromannans (HMs) in the rhizome is nearly three-fold compared to that of the leave and stem.

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Bacterial and viral pathogens can modulate the glycosylation of key host proteins to facilitate pathogenesis by using various glycosidases, particularly sialidases. Epidermal growth factor receptor (EGFR) signaling is activated by ligand-induced receptor dimerization and oligomerization. Ligand binding induces conformational changes in EGFR, leading to clusters and aggregation.

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We demonstrate that dibenzocyclooctendiones (DBCDOs) are efficient chemical reagents for the site-specific labeling of arginine-containing biomolecules. Unlike the commonly used probes, DBCDOs undergo an irreversible ring-contracted rearrangement with the guanidinium group on arginine residues under mild reaction conditions. The regioselective dual-labeled arginine residues were obtained in a one-pot reaction with our tested substrates.

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Handwriting difficulties are common in children with Attention-Deficit/Hyperactivity Disorder (ADHD), and they have been associated with lower academic achievement and self-esteem. Our aim in this study was to determine if training coordination of the head, eyes, and arm and engaging in the necessary visual concentration associated with table tennis would improve executive functions and school-based handwriting among children with ADHD. We designed a randomized controlled trial to explore the therapeutic efficacy of this table tennis training and recruited 48 children with ADHD that we randomly assigned to one of three equal-sized training groups: (a) actual table tennis, (b) simulated table tennis (exergame), or (c) a control group receiving no additional training.

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Epidemiological studies reveal that marijuana increases the risk of cardiovascular disease (CVD); however, little is known about the mechanism. Δ-tetrahydrocannabinol (Δ-THC), the psychoactive component of marijuana, binds to cannabinoid receptor 1 (CB1/CNR1) in the vasculature and is implicated in CVD. A UK Biobank analysis found that cannabis was an risk factor for CVD.

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We report an efficient and mild tandem catalytic process for the synthesis of functionalized pyrrole-3-carbaldehydes. These compounds were obtained by a one-pot three-component reaction of 5-bromo-1,2,3-triazine, terminal alkynes, and primary amines via a palladium-catalyzed Sonogashira coupling reaction, and then annulation through a silver-mediated reaction of the resulting alkynyl 1,2,3-triazines allowed for access to the multifunctionalized pyrrole-3-carbaldehydes.

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-Glycans are major constituents of several cellular glycoproteins. One-pot strategies for the synthesis of -glycans are crucial for the rapid generation of pure samples to determine their biological functions. Herein, we describe a double one-pot strategy for the synthesis of -glycans assisted by an IM-MS analysis approach for rapid screening of optimized glycosylation reaction conditions.

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Background: Colorectal cancer (CRC) is a worldwide cancer with rising annual incidence. New medications for patients with CRC are still needed. Recently, fluorescent chemical probes have been developed for cancer imaging and therapy.

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A highly diastereoselective indium-mediated allylation of 2--acetyl glycosyl sulfinylimines in brine under mild reaction conditions is reported. The method allows the achievement of a highly remarkable dichotomous selectivity for substrates, providing a single diastereoisomer of the product in 80-98% yield. With chiral ()-homoallylic sulfinamide ()- and ()- formed as key intermediates, two potent anti-influenza agents, zanamivir and zanaphosphor, were synthesized in 50% and 41% overall yields, respectively.

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  • Huntington's disease (HD) is linked to the toxic aggregation of a mutated protein called huntingtin (mHtt), which causes neuronal dysfunction.
  • Researchers developed a specific gold nanoparticle (AuNP) complex that targets and reduces the toxicity of mHtt by using a specially designed peptide, JLD1, that binds to the toxic aggregates.
  • The modified AuNPs (AuNPs-JLD1-PEI) can enter cells, break down mHtt inclusions, and have shown promising results in a larval model of HD, indicating potential new treatments for this disease.
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For decades, high-resolution H NMR spectroscopy has been routinely utilized to analyze both naturally occurring steroid hormones and synthetic steroids, which play important roles in regulating physiological functions in humans. Because the H signals are inevitably superimposed and entangled with various splitting patterns, such that the individual H chemical shift and associated coupling identities are hardly resolved. Given this, applications of thess information for elucidating steroidal molecular structures and steroid/ligand interactions at the atomic level were largely restricted.

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Secondary metabolites are structurally diverse natural products (NPs) and have been widely used for medical applications. Developing new tools to enrich NPs can be a promising solution to isolate novel NPs from the native and complex samples. Here, we developed native and deuterated chemoselective labeling probes to target phenol-containing glycopeptides by the ene-type labeling used in proteomic research.

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Partially acetylated chito-oligosaccharides (paCOSs) are bioactive compounds with potential medical applications. Their biological activities are largely dependent on their structural properties, in particular their degree of polymerization (DP) and the position of the acetyl groups along the glycan chain. The production of structurally defined paCOSs in a purified form is highly desirable to better understand the structure/bioactivity relationship of these oligosaccharides.

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