Uniform Molecular Weight Research Articles

Purification, structural characterization and immunomodulatory activity of a polysaccharide isolated from Scutellaria baicalensis stem-leaf

In our research, a novel polysaccharide (named SSP-3a) with uniform molecular weight was extracted from Scutellaria baicalensis stem-leaf. The structural analysis revealed that SSP-3a was an acidic polysaccharide with a heavy average molecular weight of 1.83 × 105 Da. By HPLC, the primary constituents of SSP-3a were mannose (11.60 %), glucuronic acid (42.99 %), glucose (23.43 %), and xylose (22.04 %). According to FT-IR and 1H NMR analysis, it was confirmed to be a β-configuration pyranose with a CO stretching vibrational peak. The immunomodulation results also showed that SSP-3a not only significantly promoted RAW264.7 cell proliferation and phagocytosis, but also stimulated the release of NO and cytokines. Furthermore, mechanistic studies suggested that SSP-3a had the ability to trigger MAPKs and NF-κB immunological signaling pathways via TLR4 receptors. The findings suggested that SSP-3a might be a beneficial active component for the food and pharmaceutical industries.

Effects of Protein on Green Tea Quality in a Milk-Tea Model during Heat Treatment: Antioxidant Activity, Foaming Properties, and Unbound Small-molecule Metabolome

Tea drinks/beverage has a long history and milk is often added to enhance its taste and nutritional value, whereas the interaction between the tea bioactive compounds with proteins has not been systematically investigated. In this study, a milk-tea model was prepared by mixing green tea solution with milk and then heated at 100°C for 15 min. The milk tea was then measured using biochemical assay, antioxidant detection kit, microscopy as well as HPLC-QTOF-MS/MS after ultrafiltration. The study found that as the concentration of milk protein increased in the milk-tea system, the total phenol-protein binding rate raised from 19.63% to 51.08%, which led to a decrease in free polyphenol content. This decrease of polyphenol was also revealed in the antioxidant capacity, including 2,2-diphenyl-1-picrylhydrazyl radical scavenging ability and ferric ion reducing antioxidant power, in a dose-dependent manner. Untargeted metabolomics results revealed that the majority of small-molecule compounds/polyphenols in tea, such as epigallocatechin gallate, (-)-epicatechin gallate, and Catechin 5,7,-di-O-gallate, bound to milk proteins and were removed by ultrafiltration after addition of milk and heat treatment. The SDS-PAGE and Native-PAGE results further indicated that small molecule compounds in tea formed covalent and non-covalent complexes by binding to milk proteins. All above results partially explained that milk proteins form conjugates with tea small-molecule compounds. Consistently, the particle size of the tea-milk system increased as the tea concentration increased, but the polymer dispersity index decreased, indicating a more uniform molecular weight distribution of the particles in the system. Addition of milk protein enhanced foam ability in the milk-tea system but reduced foam stability. In summary, our findings suggest that the proportion of milk added to tea infusion needs to be considered to maintain the quality of milk-tea from multiple perspectives, including stability, nutritional quality and antioxidant activity.

Structural analysis and biological activity of cell wall polysaccharides and enzyme-extracted polysaccharides from pomelo (Citrus maxima (Burm.) Merr.)

Pomelo peel is a valuable source of pectin, but research on its cell wall polysaccharides is limited. This study compared the cell wall polysaccharides of pomelo peel, enzyme-extracted polysaccharides of pomelo peel, and enzyme-extracted polysaccharides of whole pomelo fruit. Cell wall polysaccharides, including water-soluble pectin (WSP), chelator-soluble pectin (CSP), sodium carbonate-soluble pectin (NSP), 1 mol/L KOH soluble hemicellulose (KSH-1), and 4 mol/L KOH soluble hemicellulose (KSH-2), were obtained by sequence-extraction method. Total polysaccharides from whole pomelo fruit (TP) and peel-polysaccharides from pomelo pericarps (PP) were obtained using enzyme-extraction method. The structural, thermal, rheological, antioxidant properties, and wound healing effect in vitro were described for each polysaccharide. WSP had a uniform molecular weight distribution and high uronic acid (UA) content, suitable for commercial pectin. NSP had the highest Rhamnose (Rha)/UA ratio and a rich side chain with highest viscosity and water retention. PP displayed the highest DPPH radical scavenging activity and reducing capacity at 0.1 to 2.0 mg/mL concentration range, with an IC50 of 1.05 mg/mL for DPPH free radicals. NSP also demonstrated the highest hydroxyl radical scavenging activity and promoted Human dermal keratinocyte proliferation and migration at 10 μg/mL, suggesting potential applications in daily chemical and pharmaceutical industries.

Upgrading lignocellulosic biomass to high-value products through the pretreatment driven by bio-based ethylene glycol solvent

Sustainable processing of lignocellulosic biomass is meaningful for comprehensive biomass conversion. Here, a ball milling (BM) assisted biomass-derived ethylene glycol (BEG) pretreatment is proposed to removes nearly 90 % of the lignin and increases cellulose accessibility by 3 times than raw biomass, facilitating subsequent enzymatic saccharification or catalytic conversion for 5-hydroxymethylfurfural (HMF), achieving yields of 92.9 % and 32.6 %. The synergistic effect of BM/BEG positively impacted delignification, followed by saccharification and HMF conversion. Introduction of biomass-derived solvent recovers the lignin with a well-preserved chemical structure, uniform molecular weight, short side chains, and high purity, making it highly suitable for downstream utilization. Density functional theory revealed hydrogen bonding and good miscibility between BEG and lignin units, suggesting reaction mechanisms and pathways. Molecular dynamics simulations showed that the solubilizing effect of BEG on lignin promoted cellulase-cellulose binding, thereby enhancing saccharification efficiency. The successful use of BEG solvents to maximize the biomass value is conducive to achieve closed-loop biorefinery approaches.

Integrated Preparation of Hollow Lignin Nanoparticles as a Drug Carrier and Levulinic Acid from the Poplar Wood Prehydrolysis Liquor.

Prehydrolysis liquid (PHL) from dissolving pulp and biorefinery industries is rich in saccharides and lignin, being considered as a potential source of value-added materials and platform molecules. This study proposed an environmentally friendly and simple method to prepare morphologically controllable hollow lignin nanoparticles (LNPs) and levulinic acid (LA) from PHL. In the first step, after hydrothermal treatment of PHL with p-toluenesulfonic acid (p-TsOH), lignin with a uniform molecular weight was obtained to prepare LNPs. The prepared LNPs have an obvious hollow structure, with an average size of 490-660 nm, and exhibit good stability during 30 days of storage. When the as-obtained LNPs were used as a sustained-release agent for amikacin sulfate, the encapsulation efficiency reached over 70% and the release efficiency within 40 h reached 69.2% in a pH 5.5 buffer. Subsequently, the remaining PHL that contains saccharides was directly used for LA production under the catalysis of p-TsOH. At 150 °C for 1.5 h, the LA yield reached 58.4% and remained at 56% after 5 cycles of p-TsOH. It is worth noting that only p-TsOH was used as a reactive reagent throughout the entire preparation process. Overall, this study provided a novel pathway for the integrated utilization of PHL and showed the immense potential of the preparation and application of LNPs.

Valorization of cell wall polysaccharides extracted from Liubao brick tea residues: chemical, structural, and hypoglycemic properties.

Tea dregs, typically generated during the production of instant tea or tea beverages, have conventionally been regarded as waste material and routinely discarded. Nevertheless, contemporary research endeavors are concentrating on discovering efficient methods for utilizing the potential of this discarded resource. In this study, we employed a sequential extraction method using chemical chelating agents to extract and isolate four distinct cell wall polysaccharides, designated as CWTPS-1 through CWTPS-4, from the tea dregs of Liubao brick tea. A comprehensive investigation into their physicochemical, structural, and hypoglycemic properties was conducted. The analysis of chemical composition and physicochemical characteristics revealed that all four CWTPSs were characterized as acidic polysaccharides, albeit with varying chemical compositions and physicochemical attributes. Specifically, the xyloglucan fractions, CWTPS-3 and CWTPS-4, were found to be rich in glucose and xylose, displaying a more uniform molecular weight distribution, greater structural stability, and a more irregular surface compared to the others. Moreover, they exhibited a higher diversity of monosaccharide residues. Importantly, our research unveiled that all four CWTPSs exhibited the capacity to modulate key glucose-regulated and antioxidant enzyme activities within HepG2 cells via the IRS-1-PI3K/AKT signaling pathway, thereby ameliorating cellular insulin resistance. Furthermore, our correlation analysis highlighted significant associations between monosaccharide composition and neutral sugar content with the observed hypoglycemic activity of CWTPSs. This study highlights the potential of utilizing tea dregs as a valuable resource, making a significant contribution to the advancement of the tea industry. Furthermore, CWTPS-4 exhibits promising prospects for further development as a functional food ingredient or additive. © 2024 Society of Chemical Industry.

Indocyanine-Green-Loaded Liposomes for Photodynamic and Photothermal Therapies: Inducing Apoptosis and Ferroptosis in Cancer Cells with Implications beyond Oral Cancer.

Oral cancer represents a global health burden, necessitating novel therapeutic strategies. Photodynamic and photothermal therapies using indocyanine green (ICG) have shown promise due to their distinctive near-infrared (NIR) light absorption characteristics and FDA-approved safety profiles. This study develops ICG-loaded liposomes (Lipo-ICGs) to further explore their potential in oral cancer treatments. We synthesized and characterized the Lipo-ICGs, conducted in vitro cell culture experiments to assess cellular uptake and photodynamic/photothermal effects, and performed in vivo animal studies to evaluate their therapeutic efficacy. Quantitative cell apoptosis and gene expression variation were further characterized using flow cytometry and RNA sequencing, respectively. Lipo-ICGs demonstrated a uniform molecular weight distribution among particles. The in vitro studies showed a successful internalization of Lipo-ICGs into the cells and a significant photodynamic treatment effect. The in vivo studies confirmed the efficient delivery of Lipo-ICGs to tumor sites and successful tumor growth inhibition following photodynamic therapy. Moreover, light exposure induced a time-sensitive photothermal effect, facilitating the further release of ICG, and enhancing the treatment efficacy. RNA sequencing data showed significant changes in gene expression patterns upon Lipo-ICG treatment, suggesting the activation of apoptosis and ferroptosis pathways. The findings demonstrate the potential of Lipo-ICGs as a therapeutic tool for oral cancer management, potentially extending to other cancer types.

Unraveling the mechanisms underlying lignin and xylan dissolution in recyclable biphasic catalytic systems

Despite the exceptional performance of recyclable biphasic pretreatment systems (i.e., p-toluenesulfonic acid (TsOH)/pentanol, H2SO4/butanol, and AlCl3/MTHF) in the holistic fractionation of lignocellulosic biomass (LCB), there remains a significant gap in understanding of the intricate mechanisms governing the rapid dissolution of lignin and xylan from LCB. This study conducts comparative analyses using laboratory experiments and computational simulations to gain insights into the mechanism behind removing lignin and xylan in these systems. Under identical pretreatment conditions (140 °C, 45 min), three systems exhibited distinct levels of delignification and xylan removal. TsOH/pentanol showcased the highest levels of both delignification (83.3%) and xylan removal (98.1%), followed by H2SO4/butanol (77.9% delignification and 83.0% xylan removal), and AlCl3/MTHF (73.5% delignification and 97.2% xylan removal). Lignin characterization revealed that TsOH/pentanol and AlCl3/MTHF lignin samples boasted well-preserved β-O-4 bonds (42.4/100 Ar, 40.4/100 Ar, respectively), uniform molecular weights, and <1% sugar content. This led to high yields of phenolic monomers (TsOH/pentanol, 33.9%; AlCl3/MTHF, 33.7%) after catalytic hydrogenolysis of lignin. Furthermore, mechanistic analyses revealed that the TsOH/pentanol and AlCl3/MTHF systems exhibited the most significant interaction energy formation with the lignin model (veratrylglycerol-b-guaiacyl ether) and D-xylan model due to robust hydrogen bonding interactions, yielding energy values of −2460 kJ/mol and −2385 kJ/mol, respectively. These interactions could play pivotal roles in accomplishing notable lignin and xylan extraction.

Formation of a planar biomimetic membrane with a novel zwitterionic polymer for nanopore sequencing.

Biological membranes containing transmembrane channels play a crucial role in numerous cellular processes, and mimicking of cell membranes has garnered significant interest in various biomedical applications, particularly nanopore sequencing technology, where remarkable progress has been made with nanopore membranes. Considering the fragility of biomimetic membranes formed by artificial lipids and the limited mimicry of those formed by common block copolymers, this study developed a novel amphiphilic polymer by covalently linking hydrophilic heads of phospholipids to the ends of hydrophobic poly(dimethyl siloxane) (PDMS) chains. The absence of hydrophilic blocks allowed for good control over the polydispersity of this polymer within a narrow range. The high flexibility of PDMS chains, combined with relatively uniform molecular weights, would confer enhanced stability and robustness to polymeric membranes. Dynamic light scattering measurements and microdroplet formation tests demonstrated good amphipathic properties of these novel polymers when maintaining an appropriate hydrophilic-hydrophobic ratio. Moreover, the high similarity between the hydrophilic heads and natural phospholipids makes this polymer more compatible with biomolecules. A successful protein insertion experiment confirmed both the stability of this polymeric membrane and its compatibility with membrane proteins. As a result, this novel amphiphilic polymer exhibits great potential for biomembrane mimicking and paves a new path for material design in biomedical applications.

Facile synthesis of functionalized polysiloxanes with nonconventional fluorescence by oxa-Michael addition reaction

ABSTRACTDeveloping a novel methodology for the synthesis of functionalized polysiloxanes is highly desirable because of their extensive applications in engineering, textile, construction, electronics, and medical systems. Herein we introduce the oxa-Michael addition reaction as an efficient methodology to prepare a series of functionalized polysiloxanes from hydroxyalkyl-containing polysiloxanes and vinyl monomers using phosphazene base as the catalyst. The effects of various factors, including reaction time, feed ratio and solvent, were explored in this reaction. It was found that the reaction can be carried out under mild reaction (room temperature in 6 h to 24 h) with moderate to high conversion yields (60% to 99%). In particular, vinyl monomers with strong electron-withdrawing groups (e.g., cyano and sulfone groups) have higher reactivity, and the functionalized polysiloxanes can be obtained quantitatively or near-quantitatively. Interestingly, their molecular weights determined by gel permeation chromatography (GPC) reveal that the Si-O-Si skeletons were attacked by phosphazene base and re-arranged during the reaction, thus leading to improved molecular weights and more uniform molecular weight distributions in the final products than the original polysiloxanes. Moreover, these polysiloxanes exhibited intriguing nonconventional fluorescence due to the presence of unique chromophores, and those containing cyano and sulfone groups particularly exhibit the best fluorescence performance. More organosilicon materials could be developed under this simple strategy.

Highly Recyclable and Tough Elastic Vitrimers from a Defined Polydimethylsiloxane Network

AbstractDespite intensive research on sustainable elastomers, achieving elastic vitrimers with significantly improved mechanical properties and recyclability remains a scientific challenge. Herein, inspired by the classical elasticity theory, we present a design principle for ultra‐tough and highly recyclable elastic vitrimers with a defined network constructed by chemically crosslinking the pre‐synthesized disulfide‐containing polydimethylsiloxane (PDMS) chains with tetra‐arm polyethylene glycol (PEG). The defined network is achieved by the reduced dangling short chains and the relatively uniform molecular weight of network strands. Such elastic vitrimers with the defined network, i.e., PDMS‐disulfide‐D, exhibit significantly improved mechanical performance than random analogous, previously reported PDMS vitrimers, and even commercial silicone‐based thermosets. Moreover, unlike the vitrimers with random network that show obvious loss in mechanical properties after recycling, those with the defined network enable excellent thermal recyclability. The PDMS‐disulfide‐D also deliver comparable electrochemical signals if utilized as substrates for electromyography sensors after the recycling. The multiple relaxation processes are revealed via a unique physical approach. Multiple techniques are also applied to unravel the microscopic mechanism of the excellent mechanical performance and recyclability of such defined network.

Highly Recyclable and Tough Elastic Vitrimers from a Defined Polydimethylsiloxane Network.

Despite intensive research on sustainable elastomers, achieving elastic vitrimers with significantly improved mechanical properties and recyclability remains a scientific challenge. Herein, inspired by the classical elasticity theory, we present a design principle for ultra-tough and highly recyclable elastic vitrimers with a defined network constructed by chemically crosslinking the pre-synthesized disulfide-containing polydimethylsiloxane (PDMS) chains with tetra-arm polyethylene glycol (PEG). The defined network is achieved by the reduced dangling short chains and the relatively uniform molecular weight of network strands. Such elastic vitrimers with the defined network, i.e., PDMS-disulfide-D, exhibit significantly improved mechanical performance than random analogous, previously reported PDMS vitrimers, and even commercial silicone-based thermosets. Moreover, unlike the vitrimers with random network that show obvious loss in mechanical properties after recycling, those with the defined network enable excellent thermal recyclability. The PDMS-disulfide-D also deliver comparable electrochemical signals if utilized as substrates for electromyography sensors after the recycling. The multiple relaxation processes are revealed via a unique physical approach. Multiple techniques are also applied to unravel the microscopic mechanism of the excellent mechanical performance and recyclability of such defined network.

Characterization of cell wall polysaccharide from Cladosiphon okamuranus cultivated in different locations

SUMMARYCladosiphon okamuranus is an excellent source of fucoidan among any brown algae spp. However, the structure of polysaccharide varies significantly depending on the species, harvesting season and geographical location. To understand how geographic location affects the structure of cell wall polysaccharide, C. okamuranus cultivated in eight places (Bise, Katsuren, Yonashiro, Shikiya, Karimata, Nishihara, Hisamatsu and Ishigaki) in Ryukyu archipelago were collected during the peak harvesting time and the cell wall polysaccharide was analyzed physiochemically. The cell wall was sequentially fractionated into five fractions and its 80% was consisted of hot water fraction (HW) (60–70%) and hemicellulose‐I fraction (HC‐I) (15–20%), which mainly contained fucoidan composed of fucose (Fuc), glucuronic acid (GlcA) and sulfate (SO3−). Although the chemical composition and molecular weight of fucoidan in HW was slightly different at different places, the composition of Fuc, GlcA and SO3− was constant in the molar ratio of 1.0:0.5:0.7–1.0 respectively, suggesting that relatively similar structural fucoidan from C. okamuranus can be obtained from any geographical location in Okinawa Prefecture during peak time. However, considerable variation in the sugar composition in HC‐I was observed, despite the uniform molecular weight and SO3−. Particularly, HC‐I from Bise, where is the northern part of Okinawa Island, is composed of significantly higher amounts of Glc, Gal, Man, Xyl and morphologically thicker lateral branches compared to algae from the other parts of the island.

How to effectively and greenly prepare multi-scale structural starch nanoparticles for strengthening gelatin film (ultrasound-Fenton system)

Ultrasound (US) assisted with Fenton (US-Fenton) reaction was developed to efficiently and greenly prepare starch nanoparticles (SNPs) that were employed as nanofillers to enhance gelatin (G) film properties. Compared to Fenton reaction alone, US-Fenton reaction significantly improved preparation efficiency and dispersion of SNPs (p < 0.05). An optimal US-Fenton reaction parameter (300 mM H2O2, ascorbic acid 55 mM, US 45 min) was found to prepare SNPs with uniform sizes (50–90 nm) and low molecular weight (Mn 7.91 × 105 Da). The XRD, FT-IR, and SAXS analysis revealed that the US-Fenton reaction degraded the amorphous and crystalline zones of starch from top to down, leading to the collapse of the original layered structure starch and the progressive formation of SNPs. The different sizes of SNPs were selected to prepare the composite films. The G-SNP3 film (with 50–90 nm SNPs) showed the most outstanding UV blocking, tensile, and barrier properties. Especially, the tensile strength of G-5%SNP3 film (containing 5 % SNPs) increased by 156 % and 6 % over that of G film and G-5%SNP2 film (containing 5%SNPs with 100–180 nm), respectively. Therefore, the nanomaterial was promisingly prepared by the US-Fenton system and provided a strategy for designing and producing nanocomposite films.

Biphasic lignocellulose fractionation for staged production of cellulose nanofibers and reactive lignin nanospheres: A comparative study on their microstructures and effects as chitosan film reinforcing

The effective fractionation of lignocellulose and the enhancement of its components require formidable efforts. This study explored synergistic biorefinery routes for the holistic conversion of lignocellulose biomass to green nanomaterials through one-pot fractionation using recyclable p-toluenesulfonic acid (p-TsOH)/pentanol reagents. The potential of p-TsOH/pentanol pretreatment of aspen biomass under various temperatures (80–180 °C) for co-production of cellulose nanofibers (CNFs) and lignin nanospheres (LNSs) was investigated. The optimal pretreatment temperature, which minimizes cellulosic degradation and promotes the holistic conversion of biomass, was 120 °C. In addition to its highly digestible nature, the cellulose-rich residue produced high-quality CNFs with a diameter <100 nm, good crystallization, and thermostability, making it suitable for various applications. Lignin characterization, molecular dynamics simulation, and density functional theory analyses of the recovered lignin revealed well-protected β-O-4 bonds (47.3/100 Ar), uniform molecular weights (Mw, 2815 g/mol; Mn, 1704 g/mol; PDI, 1.65), < 1% sugar content, fewer condensed structures, and nanosize shapes (100–300 nm) due to the molecular interactions of p-TsOH and pentanol with lignin units. Moreover, 0.4% LNSs additions reduced the chitosan film thickness by 53% and enhanced its tensile strain and strength by 33 and 59%, respectively, as compared to the pure chitosan film. This study provides a sustainable platform for the co-production of biobased CNFs and LNSs using cutting-edge fractionation of LCB, which is a breakthrough toward industrial biorefineries.

Avocado seed waste bioconversion into poly(3-hydroxybutyrate) by using Cobetia amphilecti and ethyl levulinate as a green extractant

The avocado processing industry produces up to 1.3M tons of agro-waste annually. Chemical analysis of avocado seed waste (ASW) revealed that it is rich in carbohydrates (464.7 ± 21.4 g kg−1) and proteins (37.2 ± 1.5 g kg−1). Optimized microbial cultivation of Cobetia amphilecti using an acid hydrolysate of ASW, generated poly(3-hydroxybutyrate) (PHB) in a 2.1 ± 0.1 g L−1 concentration. The PHB productivity of C. amphilecti cultivated on ASW extract was 17.5 mg L−1 h−1. The process in which a novel ASW substrate was utilized has been further augmented by using ethyl levulinate as a sustainable extractant. This process achieved 97.4 ± 1.9 % recovery yield and 100 ± 1 % purity (measured by TGA, NMR, and FTIR) of the target PHB biopolymer, along with a high and relatively uniform PHB molecular weight (Mw = 1831 kDa, Mn = 1481 kDa, Mw/Mn = 1.24) (measured by gel permeation chromatography), compared to PHB polymer extracted by chloroform (Mw = 389 kDa, Mn = 297 kDa, Mw/Mn = 1.31). This is the first example of ASW utilization as a sustainable and inexpensive substrate for PHB biosynthesis and ethyl levulinate as an efficient and green extractant of PHB from a single bacterial biomass.

Synergistic effects of peracetic acid and oxalic acid on structural transformation of eucalyptus and its conversion

Biomass pretreatment solvent plays an important role in the utilization of lignocellulosic feedstocks. In this study, the synergistic effects of peracetic acid and oxalic acid (PAO) were investigated as a pretreatment solvent for maximizing cellulose conversion as well as recovering biologically transformable lignin. The PAO pretreatment with 4.5% oxalic acid and 2.0% peracetic acid effectively fractionated lignin (85.4%) under a mild temperature (140 °C) and resulted in a high glucose release (758 mg/g biomass) from the pretreated eucalyptus. Also, the PAO pretreatment could fractionate and deconstruct lignin to low molecular weight (1231 g/mol) aromatics with 5.8% of β-O-4 linkages and a relatively uniform molecular weight distribution (PDI 1.3). The pretreatment using PAA and OA enhanced not only the hydrolysis of cellulose but also the recovery of biologically transformable lignin as a value-added coproduct for a successful biorefinery approach.

Synthesis of Linear and Cyclic Discrete Oligomers with Defined Sequences via Efficient Anionic Coupling Reaction

We hereby report a new strategy to prepare sequence-defined discrete oligomers with uniform molecular weight through carbanionic addition and coupling reactions using specific monomers possessing 1,1-diphenylethylene (DPE) and tert-butyldimethylsilyloxy (TBS) moieties. The strategy allows the molecular weight growth by iterative attaching of the sec-butyllithium (s-BuLi) activated monomer or dimer unit to the halomethyl end-group, released from deprotection of TBS, of the proceeding oligomer starting from a dichloromethyl core. A series of linear discrete oligomers with alternating and ABCD/ACBD sequences are synthesized. These linear sequence-defined oligomers are subsequently modified with double vinyl groups and cyclized through ring-closing metathesis (RCM) reaction into corresponding sequence-defined macrocycles. The molecular structures of the linear and cyclic oligomers are analyzed by using size exclusion chromatography (SEC), nuclear magnetic resonance (NMR), and matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS). The features of the present approach are the presynthesized monomers or dimers with specific functionalities, the efficient carbanionic reactions, as well as the easy separation of the products due to the increasing difference between the molecular weights of the monomer/dimer and the products. More interestingly, sequence and topology effects were observed on Förster resonance energy transfer (FRET) measurements using naphthalene (donor) and pyrene (acceptor) functionalized linear and cyclic ABCD/ACBD oligomers having identical molecular weights and compositions for the two sequences.

Therapeutic Drug Monitoring of Antibody Drugs.

In recent years, many antibody drugs that play an important role in the pharmacotherapy of several diseases have been developed. Antibody drugs exhibit immunogenicity in vivo leading to the development of antibodies against the antibody drug (anti-drug antibody). Nonetheless, other factors also affect the pharmacokinetics of antibody drugs. Recently, therapeutic drug monitoring (TDM) of infliximab was introduced for personalized medicine. However, the usefulness of TDM in antibody therapy remains unclear. In addition to intervention studies, real-world data analysis is important. Unlike small-molecule drugs, antibody drugs do not have a uniform molecular weight; therefore, using the conventional analysis methods, it is impossible to determine the true pharmacokinetic outcomes of these agents. To analyze structural changes of antibody drugs in the body, new technologies are necessary. In the future, along with the development of new drugs, the establishment of novel analytical methods is essential to facilitate the promotion of personalized medicine.

Cloning, expression and characterization of metalloproteinase HypZn from Aspergillus niger.

A predicted metalloproteinase gene, HypZn, was cloned from Aspergillus niger CGMCC 3.7193 and expressed in Pichia pastoris GS115, and the physicochemical characteristics of recombinant HypZn were investigated after separation and purification. The results showed that the specific activity of the purified HypZn reached 1859.2 U/mg, and the optimum temperature and pH value of HypZn were 35°C and 7.0, respectively. HypZn remained stable both at 40°C and at pH values between 5.0 and 8.0. The preferred substrate of HypZn was soybean protein isolates, and the Km and Vmax values were 21.5 μmol/mL and 4926.6 μmol/(mL∙min), respectively. HypZn was activated by Co2+ and Zn2+ and inhibited by Cu2+ and Fe2+. The degree of soybean protein isolate hydrolysis reached 14.7%, and the hydrolysates were of uniform molecular weight. HypZn could tolerate 5000 mM NaCl and completely lost its activity after 30 min at 50°C. The enzymological characterizations indicated that HypZn has great application potential in the food industry, especially in fermented food processing.