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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2024 · IF 7.7

Identification and functional characterization of a novel cystatin in amphioxus, ancient origin of vertebrate type-2 cystatin homologues

Tianren Wang,Jingru Gao,Jinghan Xu,Yuxiang Hong,Ronghuan Du,Xian Zheng,Peng Wang

Cystatins are well known as a vast superfamily of functional proteins participated in the reversible competitive inhibition of cysteine proteases. Currently, increasing evidences point to the extensive phylogenetic diversity and crucial immune roles of type-2 cystatins in the vertebrate species. However, no information is available regarding the homologue in cephalochordate amphioxus, the representative of most basal living chordates, whose immune regulation are still ambiguous. Here, we clearly identified the presence of type-2 cystatin gene in amphioxus Branchiostoma japonicum , termed Bjcystatin-2, which was structurally characterized by typical wedge-shaped cystatin feature. Evolutionary analyses revealed that Bjcystatin-2 is the putative ancestral type-2 cystatin for chordates, with gene diversity emerging through duplication events. The expression of Bjcystatin-2 showed tissue-specific profile and was inducible upon invasive pathogens. Significantly, the recombinant Bjcystatin-2 exhibited not merely cathepsin L inhibitory activity, but also the ability to bind with bacteria and their characteristic molecules. Furthermore, Bjcystatin-2 also showed the capacity to enhance the macrophage-driven bacterial phagocytosis and to attenuate the generation of pro-inflammatory cytokines within macrophages. In summary, these findings demonstrate that Bjcystatin-2 exhibits dual role acting as both a protease inhibitor and an immunoactive molecule, greatly enriching our understanding of immune defense mechanisms of type-2 cystatin within the amphioxus.

CAS / MDL: 70382-26-2
研究领域: 免疫学 · 分子生物学 · 进化生物学 · 蛋白质组学
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EUROPEAN JOURNAL OF ORGANIC CHEMISTRY · 2013 ·Vol. 2013 ·期 32 ·7411-7420 · IF 3.344

BF3·OEt2-Promoted Tandem O-Arylation/Hydroxylation: Efficient Synthesis of 2-Hydroxyflavanones from Triazenylaryl-Substituted Diketones

Zhengkai Chen,Weijun Yang,Lijun Xu,Lili Zhang,Maozhong Miao,Hongjun Ren

Graphical Highly substituted 2-hydroxyflavanones can be obtained through a tandem O -arylation/hydroxylation process from triazenylaryl-substituted diketones in the presence of a Lewis acid. A transition-metal-free tandem O -arylation/hydroxylation approach has been developed for the efficient synthesis of highly substituted 2-hydroxyflavanones from triazenylaryl-substituted diketones. The intermediate benzopyrylium cation may be involved in these reactions.

研究领域: 有机化学 · 药物化学
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Small · 2024 · IF 13

Microneedle Patch for Transdermal Sequential Delivery of KGF-2 and aFGF to Enhance Burn Wound Therapy

Huacheng He,Wen Huang,Shihui Zhang,Jie Li,Jian Zhang,Bingxin Li,Jie Xu,Yuting Luo,Huiling Shi,Yue Li,Jian Xiao,Odinaka Cassandra Ezekiel,Xiaokun Li,Jiang Wu

Severe burn wounds usually destroy key cells’ functions of the skin resulting in delayed re-epithelization and wound regeneration. Promoting key cells’ activities is crucial for burn wound repair. It is well known that keratinocyte growth factor-2 (KGF-2) participates in the proliferation and morphogenesis of epithelial cells while acidic fibroblast growth factor (aFGF) is a key mediator for fibroblast and endothelial cell growth and differentiation. However, thick eschar and the harsh environment of a burn wound often decrease the delivery efficiency of fibroblast growth factor (FGF) to the wound site. Therefore, herein a novel microneedle patch for sequential transdermal delivery of KGF-2 and aFGF is fabricated to enhance burn wound therapy. aFGF is first loaded in the nanoparticle (NP aFGF ) and then encapsulated NP aFGF with KGF-2 in the microneedle patch (KGF-2/NP aFGF @MN). The result shows that KGF-2/NP aFGF @MN can successfully get across the eschar and sequentially release KGF-2 and aFGF. Additional data demonstrated that KGF-2/NP aFGF @MN achieved a quicker wound closure rate with reduced necrotic tissues, faster re-epithelialization, enhanced collagen deposition, and increased neo-vascularization. Further evidence suggests that improved wound healing is regulated by significantly elevated expressions of hypoxia-inducible factor-1 alpha (HIF-1ɑ) and heat shock protein 90 (Hsp90) in burn wounds. All these data proved that KGF-2/NP aFGF @MN is an effective treatment for wound healing of burns.

研究领域: 生物医学工程 · 药剂学 · 组织修复与再生
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IONICS · 2024 · IF 2.4

Sea urchin-like sulfur-doped Ni(OH)2 as an efficient electrocatalyst for oxygen evolution reaction

Wu Fang,Ge Jin-Long,Zhu Yujun,Jiao Yuhong,Wu Zhong,Feng Chao,Zhao Yupei,Li Qiu

The development of high-performance and cost-effective electrocatalysts toward the oxygen evolution reaction (OER) is remarkably desirable but challenging. Herein, we design and fabricate a sea urchin-like S-doped Ni(OH) 2 electrocatalyst on nickel foam using a simple hydrothermal method, followed by treatment with Na 2 S solution. The introduction of S not only modulates the electronic structure of Ni(OH) 2 , but also improves the electronic conductivity, thus enhancing the OER performance of Ni(OH) 2 . Owing to the free-standing feature, modified electronic structure, and sea urchin-like structure, the optimized S-Ni(OH) 2 –30 min delivers excellent OER performance with overpotentials of 306 and 392 mV at 10 and 100 mA cm −2 , respectively, Tafel slope of 89.2 mV dec −1 , and stability for 30 h at 50 mA cm −2 . This work demonstrates the importance of incorporating S in Ni(OH) 2 to optimize the electronic structure for improving OER activity and provides a promising pathway to synthesize Ni(OH) 2 -based electrocatalysts.

研究领域: 材料科学 · 电化学
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NEW JOURNAL OF CHEMISTRY · 2025 · IF 2.5

Synthesis of dithieno[3,2-b:2′,3′-d]benzo[1,2-c][1,2,5]thiadiazole-cored polymerized small-molecule acceptors with ordered backbone stacking and their application in all-polymer solar cells

Tiantian Wang,Jianhong Wei,Furong Shi,Hejie Wang,Jinye He,Xudong Lv,Yuan Zhou,Pengzhi Guo,Chenglong Wang,Yangjun Xia

In recent years, polymerized small molecule acceptors (PSMAs) have emerged as a promising strategy that combines the strong absorption of small molecules with the film-forming ability and stability of polymers, thereby greatly boosting the performance of all-polymer solar cells (all-PSCs). We designed a non-fused acceptor, DTBT-IC, and its polymeric counterpart, PDTBT-Br-T, by selecting DTBT as the core, bithiophene as the π-bridge, and IC as the terminal group. PDTBT-Br-T was synthesized via Stille coupling and used with PM6 as the donor to fabricate organic solar cells. The PDTBT-Br-T-based device delivered superior performance, with a VOC of 1.050 V, JSC of 9.32 mA cm−2, FF of 45.33%, and a PCE of 4.44%, outperforming the DTBT-IC-based counterpart. Morphological and structural analyses revealed that PDTBT-Br-T exhibits more ordered backbone stacking and defined phase separation, enhancing exciton dissociation and charge transport, and suppressing energy loss. The study highlights that polymerization of DTBT-IC enhances intermolecular packing and microstructure, offering critical design insights for efficient all-PSCs.

研究领域: 材料科学 · 高分子化学 · 有机电子学 · 光伏技术
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Molbank · 2024 ·Vol. 2024 ·期 2 ·M1828 · IF 0.6

Hept-6-en-1-yl Furan-2-carboxylate

Zhongwei Wang,Lin Song,Yukun Qin

This study aims to develop an efficient and green one-pot method for the synthesis of 6-en-1-yl furan-2-carboxylic acid heptyl ester. Initially, using furfural as the starting substrate, hept-6-en-1-yl furan-2-carboxylate was prepared using a one-pot method. This study developed a new experimental scheme for preparing ester compounds, using cuprous chloride as a catalyst and tert butyl hydrogen peroxide as an oxidant to prepare furoic acid. Without the need for intermediate treatment, the target product can be directly obtained from furfural by adding 7-bromo-1-heptene, TBAB, and potassium carbonate. This method effectively utilizes furfural as a platform chemical, demonstrating its potential for synthesizing high-value chemicals. The entire synthesis process is simple and efficient, following the principles of green chemistry.

研究领域: 有机化学 · 绿色化学 · 合成化学
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JOURNAL OF MEMBRANE SCIENCE · 2024 · IF 8.4

Bicontinuous porous substrates by polysulfone/2-pyrrolidone binary system for high-performance forward osmosis membranes

Nan Sun,Shucheng Mo,Yuanhang Cai,Yingshuai Zhao,Yaling Han,Yijun Zheng,Tao He

Forward osmosis (FO) has shown great promise in concentrating enriched lithium brine during lithium extraction from salt-lake brine due to low energy consumption and ecologically friendliness. The effective utilization of enormous osmotic pressure of freely available MgCl 2 onsite requires highly selective FO membranes with high flux, which calls for thin-film composite forward osmosis (TFC-FO) membranes of highly interconnected substrate and defect-free separation layer. Herein, for the first time, we employed 2-Pyrrolidone (2-PD) as the solvent to prepare FO substrates via the non-solvent induced phase separation (NIPS) for preparing TFC FO membranes. Owing to its weak solubility, the PSf/2-PD polymer solution shows high viscoelasticity, resulting in spinodal demixing and a bicontinuous porous structure, unlike the closed finger-like pore structure observed in the PSf/DMAc binary system. By further reducing the casting humidity and coagulation bath temperature, the substrate surface pore size was optimized to prepare high-performance TFC-FO membranes: the TFC-30%-3 exhibits a water flux of 20.0 LMH and low specific reverse salt flux of 0.23 g/L at AL-FS mode, showing competitive performance compared to the state-of-the-art membranes. These results imply that 2-PD, as an environmentally friendly alternative to traditional solvents, shows significant promise for FO substrate preparation using a simple polymer/solvent binary system.

CAS / MDL: 108-45-2
研究领域: 材料科学 · 环境工程
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DALTON TRANSACTIONS · 2022 ·Vol. 51 ·期 32 ·12352-12361 · IF 4.569

Thermal enhancing effect of upconversion luminescence in Er3+/Yb3+ co-doped Cs3BiSr(P2O7)2 phosphors

Hongqiang Cui,Yongze Cao,Yuhang Zhang,Lei Li,Guojian Li,Sai Xu,Yichao Wang,Jinsu Zhang,Baojiu Chen

A series of Er3+/Yb3+ co-doped Cs3BiSr(P2O7)2 (CBSPO) phosphors with significant thermal enhancement were successfully prepared using the solid-state method and the thermal-enhancing effect was studied in detail. When the temperature increased from 303 to 723 K, the upconversion luminescence (UCL) emission intensities of 2H11/2 → 4I15/2 and 2H11/2 + 4S3/2 → 4I15/2 of Er3+ in CBSPO:0.1Er3+/0.2Yb3+ were enhanced 22.81 and 10.06 times under 980 nm laser excitation, respectively. Meanwhile, the UCL color of the sample obviously changed from orange to green with the increase in temperature. Furthermore, the UCL thermal enhancement mechanism was demonstrated, which originates from phonon-assisted transitions. In addition, the maximum absolute temperature sensitivity for CBSPO:0.1Er3+/0.2Yb3+ was calculated to be 0.01026 K−1 at 563 K via luminescence intensity ratio (LIR) technology. All the results show that the CBSPO:Er3+/Yb3+ phosphors can be used for safety warning and temperature measurement at high temperatures.

研究领域: 材料科学 · 光学
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ACS Synthetic Biology · 2025 · IF 3.9

Thermostable Coenzyme a Ligase for Efficient Biosynthesis of 2-Pyrrolidone via Protein and Fermentation Engineering

Bicheng Yu,Wei Song,Shenjie Wang,Wanqing Wei,Guipeng Hu,Xiaomin Li,Cong Gao,Jia Liu,Jian Wen,Jing Wu

2-Pyrrolidone is an important chemical intermediate with broad applications in the materials and pharmaceutical industries. Traditional petrochemical synthesis methods pose significant environmental challenges. In the case of biosynthesis, the limited thermostability of coenzyme A ligase (CaiC) represents a major barrier to industrial-scale production. This study focused on enhancing the thermostability and catalytic efficiency of EcCaiC through protein engineering. Conserved sequences were identified, and flexible regions were targeted for virtual mutagenesis using FoldX and Rosetta. The resulting mutant, M3, exhibited a 7.86-fold increase in half-life(t1/2) at 55 °C and a Tm of 59.3 °C. Additionally, the catalytic efficiency (kcat/Km) of M3 improved by 52.8%, reaching 5.73 mM–1 s–1 compared to the wild type. Subsequently, EcCaiCM3 was introduced into Corynebacterium glutamicum S9114, with targeted knockout of byproduct synthesis genes. Finally, fed-batch fermentation in a 5 L bioreactor achieved a 2-pyrrolidone yield of 58.28 g/L, a glucose conversion rate of 0.32 g/g, and a productivity of 0.97 g/L/h. This work establishes an efficient biosynthetic platform for 2-pyrrolidone, providing a robust foundation for its industrial production.

研究领域: 生物化学 · 工业微生物学 · 蛋白质工程
✓ 已验证 DOI PubMed 高影响因子
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ChemMedChem · 2025 · IF 3.4

Discovery of Safe COX-2 Inhibitors: Achieving Reduced Colitis Side Effects through Balanced COX Inhibition

Xinlin Zhu,Qin Li,Junhui Wu,Zhiran Ju

Graphical In recent years, the development of COX-2 inhibitors has shifted from a focus on highly selective inhibition to emphasizes more moderate selectivity. This study presents a potent balanced COX-2 inhibitor, compound 21d, which effectively alleviates histological damage and provides protection against DSS-induced colitis. The severe adverse effects associated with imbalanced cyclooxygenase-2 (COX-2) inhibition continue to pose significant challenges in the development of contemporary anti-inflammatory drugs. In recent years, the approach to COX-2 inhibitor drug development has shifted from a focus on highly selective inhibition of COX-2 to a strategy that emphasizes more moderate selectivity. The amino acid sequence and structural similarities between inducible COX-2 and constitutive cyclooxygenase-1 (COX-1) isoforms present both substantial opportunities and challenges for the design of next generation of balanced COX-2 inhibitors. As part of our ongoing research into the discovering novel and safer COX-2 inhibitors, we reported herein a highly potent and balanced COX-2 inhibitor 21 d (IC 50 value=1.35 μM, selectivity profile (IC 50 (COX-1)/IC 50 (COX-2)=22.34)). In vivo assays demonstrated that 21 d significantly alleviated histological damage and provided robust protection against dextran sulfate sodium (DSS)-induced acute colitis.

研究领域: 药理学 · 分子生物学 · 药物开发
✓ 已验证 DOI PubMed 高影响因子
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ANALYTICAL CHEMISTRY · 2021 · IF 6.986

Aptamer-Functionalized Nanochannels for One-Step Detection of SARS-CoV-2 in Samples from COVID-19 Patients

Liu Shi,Lin Wang,Xuemei Ma,Xiaona Fang,Liangliang Xiang,Yongxiang Yi,Jinlong Li,Zhaofeng Luo,Genxi Li

With the outbreak of COVID-19, which is fast transmitting and highly contagious, the development of rapid, highly specific, and sensitive detection kits has become a research hotspot. The existing assay methods for SARS-CoV-2 are mainly based on enzymatic reactions, which require expensive reagents, hindering popular use, especially in resource-constrained areas. Herein, we propose an aptamer-based method for the assay of SARS-CoV-2 via binding of the spike protein using functionalized biomimetic nanochannels. To get the analogous effect of human ACE2, a receptor for the spike protein, the aptamer to bind to the spike S1 protein has been first screened by a SELEX technique and then immobilized on the previously prepared nanochannels. In the presence of SARS-CoV-2, the changes in steric hindrance and charge density on the surface of the nanochannels will affect the ion transport, along with a rapid electrochemical response. Our method has been successfully applied to detect the viral particles in clinical pharyngeal swab specimens in one step without sample treatment. We expect this rapid, reagent-free, and sensitive assay method to be developed as a useful tool for diagnosing COVID-19.

研究领域: 生物医学工程 · 病毒学 · 诊断学
✓ 已验证 DOI PubMed 高影响因子
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ORGANIC & BIOMOLECULAR CHEMISTRY · 2025 · IF 2.7

NBS-mediated C-selenocyanation/cyclization of enaminones with KSeCN: a mild and efficient synthesis of 2-aminoselenazoles

Fei Yuan,Yiyuan Xin,Caifeng Yuan,Zhuo Chen,Tongling Qin,Wenxia Hu,Jiahuan Duan,E Tang

A simple, exogenous-base-free, and NBS-mediated C-selenocyanation/cyclization reaction of enaminones with KSeCN under mild conditions, providing a facile route to 2-aminoselenazole products, has been developed. This efficient protocol is postulated to first undergo the NBS-oxidated polarity reversal of the reactive SeCN- anion to form N-selenocyanosuccinimide as an electrophilic selenium source, which can induce the C-selenocyanation of enaminones and enamino esters, followed by a nucleophilic cyclization promoted by in-situ yielded HBr.

研究领域: 有机化学 · 合成化学 · 硒化学
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