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1.
J Colloid Interface Sci ; 610: 953-969, 2022 Mar 15.
Article in English | MEDLINE | ID: mdl-34865737

ABSTRACT

The semiconductor-based photocatalysts with local surface plasmon resonance (LSPR) effect can extend light response to near-infrared region (NIR), as well as promote charge-carriers transfer, which provide a novel insight into designing light-driven photocatalyst with excellent photocatalytic performance. Here, we designed cost-effective wide-spectrum Zn2In2S5/W18O49 composite with enhanced photocatalytic performance based on a dual-channel charge transfer pathway. Benefiting from the synergistic effect of Z-scheme heterostructure and unique LSPR effect, the interfacial charge-carriers transfer rate and light-absorbing ability of Zn2In2S5/W18O49 were enhanced significantly under visible and NIR (vis-NIR) light irradiation. More reactive oxygen species (ROS) were formed by efficient molecular oxygen activation, which were the critical factors for both Escherichia coli (E. coli) photoinactivation and tetracycline (TC) photodegradation. The enhancement of molecular oxygen activation (MOA) ability was verified via quantitative analyses, which evaluated the amount of ROS through degrading nitrotetrazolium blue chloride (NBT) and p-phthalic acid (TA). By combining theoretical calculations with diverse experimental results, we proposed a credible photocatalytic reaction mechanism for antibiotic degradation and bacteria inactivation. This study develops a new insight into constructing promising photocatalysts with efficient photocatalytic activity in practical wastewater treatment.


Subject(s)
Electrons , Escherichia coli , Anti-Bacterial Agents/pharmacology , Catalysis , Oxygen , Zinc
2.
Viral Immunol ; 33(6): 468-476, 2020.
Article in English | MEDLINE | ID: mdl-32315577

ABSTRACT

As a zoonotic disease, ovine contagious pustular dermatitis (Orf) is a serious threat to sheep as well as humans. Orf virus (ORFV) interferon resistance protein (VIR) is the principal virulence protein that encodes a dsRNA-binding protein to inhibit host antiviral response. p53 is one of the key proteins of the host antiviral innate immunity. It not only enhances type I interferon secretion but also induces apoptosis in infected cells, and plays a crucial role in the immune response against various viral infections. However, it remains to be elucidated what role p53 plays in ORFV replication and whether ORFV's own protein VIR regulates p53 expression to promote self-replication. In this study, we showed that p53 has an antiviral effect on ORFV and can inhibit ORFV replication. In addition, ORFV nonstructural protein VIR interacts with p53 and degrades p53, which inhibits p53-mediated positive regulation of downstream antiviral genes. This study provides new insight into the immune evasion mediated by ORFV and identifies VIR as an antagonistic factor for ORFV to evade the antiviral response.


Subject(s)
Host Microbial Interactions/genetics , Orf virus/genetics , Tumor Suppressor Protein p53/genetics , Viral Proteins/genetics , Virus Replication/genetics , Animals , Cell Line , Cricetinae , Ecthyma, Contagious/virology , Fibroblasts/immunology , Fibroblasts/virology , Gene Expression Regulation, Viral , Goats , Immune Evasion/genetics , Immunity, Innate , Kidney/cytology , Orf virus/physiology , Sheep , Skin/cytology , Viral Proteins/metabolism
3.
Comput Biol Chem ; 80: 324-332, 2019 Jun.
Article in English | MEDLINE | ID: mdl-31078911

ABSTRACT

Various protein kinases are implicated in the pathogenesis of human cervical cancer and many kinase inhibitors have been used to regulate the activity of protein kinases involved in the disease signaling networks. In the present study, a systematic kinase-inhibitor interactome is created for various small-molecule inhibitors across diverse cervical cancer-related kinases by using ontology enrichment, molecular docking, dynamics simulation and energetics analysis. The interactome profile is examined in detail with heatmap analysis and heuristic clustering to derive promising inhibitors that are highly potential to target the kinome of human cervical cancer in a multi-target manner. A number of hit and unhit inhibitors are selected and their cell-suppressing effects are tested against human cervical carcinoma HeLa, from which several inhibitor compounds with high cytotoxicity are successfully identified. A further kinase assay confirms that these inhibitors can generally target their noncognate kinases HER3 and BRaf in cervical cancer with a high or moderate activity; the activity profile are comparable with or even better than that of cognate kinases inhibitors, with IC50 values ranging between 4.8 and 340.6 nM for HER3 and between 37.2 and 638.2 nM for BRaf. This work would help to identify those unexpected kinase-inhibitor interactions in human cervical cancer and to develop new and efficient therapeutic strategy combating the disease.


Subject(s)
Protein Kinase Inhibitors/pharmacology , Protein Kinases/metabolism , Uterine Cervical Neoplasms/enzymology , Catalytic Domain , Drug Screening Assays, Antitumor , Female , Gene Ontology , HeLa Cells , Humans , Molecular Docking Simulation , Molecular Dynamics Simulation , Molecular Structure , Protein Binding , Protein Kinase Inhibitors/chemistry , Protein Kinase Inhibitors/metabolism , Protein Kinases/chemistry , Protein Kinases/genetics , Small Molecule Libraries/chemistry , Small Molecule Libraries/metabolism , Small Molecule Libraries/pharmacology , Uterine Cervical Neoplasms/drug therapy , Uterine Cervical Neoplasms/genetics
4.
Immunobiology ; 224(3): 383-387, 2019 05.
Article in English | MEDLINE | ID: mdl-30853309

ABSTRACT

Tumor progression locus 2 (TPL2) is a serine/threonine kinase that belongs to the MAP3K family. The activated TPL2 regulates the innate immune-relevant signaling pathways, such as ERK, JNK, and NF-κB, and the differentiation of immune cells, for example, CD4+ T and NK cells. Therefore, TPL2 plays a critical role in regulating the innate immune response. The present review summarizes the recent advancements in the TPL2-regulated innate immune response.


Subject(s)
CD4-Positive T-Lymphocytes/immunology , MAP Kinase Kinase Kinases/metabolism , Proto-Oncogene Proteins/metabolism , Animals , Cell Differentiation , Chemokines/metabolism , Humans , Immunity, Innate , MAP Kinase Kinase Kinases/genetics , MAP Kinase Signaling System , Macrophage Activation , Neutrophil Activation , Proto-Oncogene Proteins/genetics
5.
Sci Total Environ ; 668: 730-742, 2019 Jun 10.
Article in English | MEDLINE | ID: mdl-30865904

ABSTRACT

Magnetic materials usually exhibit advanced performance in many areas for their easy separating and recycle ability. In this study, silver iodide/copper ferrite (AgI/CuFe2O4) catalysts with excellent magnetic property were successfully synthesized and characterized by a series of techniques. Two typical bacteria Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) were applied to estimate the photocatalytic inactivation performance of obtained AgI/CuFe2O4 catalysts. Results revealed that the AgI/CuFe2O4 (12.5% AgI) composite could absolutely inactivate 3 × 109 CFU/mL E. coli and 2.7 × 108 CFU/mL S. aureus cells severally in 50 min and 40 min under visible light irradiation, which showed a much higher photo-disinfection activity than monomers. Transmission electron microscopy was used to study the biocidal action of this nanocatalyst, the results confirmed that the treated E. coli cells were damaged, the nanocatalyst permeated into cells and resulting in death of cells. Besides, it was found that the destruction of bacterial membrane together with substantial leaked potassium ion (K+) which caused by the photo-generated reactive species superoxide radical (O2-) and holes (h+) could be the direct disinfection principles. For a deep insight into practical applications, the influences of different catalyst concentrations and reaction pH were also taken into discussion in details. The overall results indicated the novel photocatalyst with strong redox capacity and outstanding reusability can be widely employed in bacteria elimination.


Subject(s)
Disinfection/methods , Light , Bismuth , Catalysis , Escherichia coli/physiology , Ferric Compounds , Staphylococcus aureus/physiology
6.
J Colloid Interface Sci ; 513: 852-865, 2018 Mar 01.
Article in English | MEDLINE | ID: mdl-29227925

ABSTRACT

In this work, the novel ternary AgBr/Ag/PbBiO2Br Z-scheme photocatalysts were synthesized via a CTAB-assisted calcination process. The AgBr/Ag/PbBiO2Br composites were employed for the degradation of rhodamine B (RhB) and antibiotic bisphenol A (BPA) under visible light irradiation. Results showed that the obtained AgBr/Ag-3/PbBiO2Br displayed optimal photocatalytic performance, which could remove almost all RhB within 25 min and effectively decompose 82.3% of BPA in 120 min. Three-dimensional excitation-emission matrix fluorescence spectra (3D EEMs) were utilized for the purposes of fully grasping the behaviors of RhB molecules during the reaction process. Meanwhile, the effects of initial RhB concentration and co-existent electrolytes were investigated from the viewpoint of practical application. In addition, there was no obvious loss in degradation efficiency even after four cycles. The enhanced photocatalytic performances of AgBr/Ag/PbBiO2Br could be credited to the accelerated interfacial charge transfer process and the improved separation of the photogenerated electron-hole pairs. The existence of a small amount of metallic Ag played a significant role in preventing AgBr from being further photocorroded, resulting in the formation of a stable Z-scheme photocatalyst system. This study demonstrated that using metallic Ag as an electron mediator to construct Z-scheme photocatalytic system provided a feasible strategy in promoting the stability of Ag-based semiconductors.

7.
Chemosphere ; 184: 347-357, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28605705

ABSTRACT

Nanotechnology has great potential in water purification. However, the limitations such as aggregation and toxicity of nanomaterials have blocked their practical application. In this work, a novel copper nanoparticles-decorated graphene sponge (Cu-GS) was synthesized using a facile hydrothermal method. Cu-GS consisting of three-dimensional (3D) porous graphene network and well-dispersed Cu nanoparticles exhibited high antibacterial efficiency against Esherichia coli when used as a bactericidal filter. The morphological changes determined by scanning electron microscope and fluorescence images measured by flow cytometry confirmed the involvement of membrane damage induced by Cu-GS in their antibacterial process. The oxidative ability of Cu-GS and intercellular reactive oxygen species (ROS) were also determined to elucidate the possible antibacterial mechanism of Cu-GS. Moreover, the concentration of released copper ions from Cu-GS was far below the drinking water standard, and the copper ions also have an effect on the antibacterial activity of Cu-GS. Results suggested that Cu-GS as a novel bactericidal filter possessed a potential application of water disinfection.


Subject(s)
Anti-Bacterial Agents/pharmacology , Escherichia coli/drug effects , Graphite/chemistry , Metal Nanoparticles/chemistry , Water Purification/methods , Copper/chemistry , Disinfection , Nanotechnology/methods
8.
J Huazhong Univ Sci Technolog Med Sci ; 35(6): 898-903, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26670443

ABSTRACT

Zinc finger of the cerebellum (ZIC1), one of ZIC family genes, has been shown to play important roles in many cancers such as gastric cancer and breast cancer. However, there is little known about the expression and significance of ZIC1 in endometrial cancer. The aim of this study was to determine the expression pattern and clinicopathological significance of ZIC1 in endometrial cancer. The mRNA and protein expression of ZIC1 in endometrial cancer tissues was detected using the reverse-transcription polymerase chain reaction and Western blotting, respectively. Immunostaining of ZIC1 in 99 endometrial cancer samples was examined and its associations with clinicopathological parameters were analyzed. Hec-1-B cells were transfected with ZIC1-shRNA or sc-shRNA, and cell proliferation was assayed. Hec-1-B cells stably transfected with ZIC1-shRNA or sc-shRNA were subcutaneously inoculated into nude mice, and the tumor weight was measured. A significantly increased expression of ZIC1 mRNA and protein was observed in endometrial cancer tissues compared to that in normal endometrial tissues (P<0.05). Immunohistochemical analysis showed that strong cytoplasmic immunostaining of ZIC1 was observed in almost all endometrial cancer samples (90/99) while light and moderate immunostaining of ZIC1 was only detected in 17 of 30 (56.7%) normal tissues. Moreover, up-regulation of ZIC1 was significantly correlated with age, disease stage, TNM stage and FIGO stage (P<0.05). The down-regulated expression of ZIC1 contributed to the inhibition of cell proliferation, and inhibited the growth of tumor. It was concluded that ZIC1 is over-expressed in endometrial cancer tissue but not in normal tissue, and positively correlated to the malignant biological behavior of endometrial carcinogenesis.


Subject(s)
Endometrial Neoplasms/metabolism , Transcription Factors/metabolism , Endometrial Neoplasms/pathology , Female , Humans , Middle Aged , RNA, Messenger/genetics , Transcription Factors/genetics
9.
Bioresour Technol ; 126: 101-6, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23073095

ABSTRACT

This study constructed a microbial fuel cell (MFC) using Fe(II)-EDTA catalyzed persulfate as the cathode solutions to decolorize Orange G (OG) and harvest electricity simultaneously. Chelated Fe(2+) could activate persulfate to generate sulfate free radicals (SO(4)(-)) which with high oxidation potential (E(0)=2.6 V) can degrade azo dyes. The influence of some important factors such as pH value of cathode solutions, dosages of K(2)S(2)O(8), Fe(2+) and EDTA were investigated in a two-chamber microbial fuel cell. Under an optimal condition, the maximum power density achieved 91.1 mW m(-2), the OG removal rate was 97.4% and the K(2)S(2)O(8) remaining rate was 47.3% after 12 h. The OG degradation by Fe(II)-EDTA catalyzed persulfate was found to follow the second-order kinetic model.


Subject(s)
Azo Compounds/chemistry , Bioelectric Energy Sources , Coloring Agents/chemistry , Edetic Acid/chemistry , Ferrous Compounds/chemistry , Potassium Compounds/chemistry , Sulfates/chemistry , Biodegradation, Environmental , Catalysis , Color , Electricity , Electrodes , Hydrogen-Ion Concentration , Ions , Kinetics
10.
Acta Biochim Biophys Sin (Shanghai) ; 36(2): 141-6, 2004 Feb.
Article in English | MEDLINE | ID: mdl-14970911

ABSTRACT

Programmed death-1 (PD-1) is a costimulatory molecule of CD28 family expressed on activated T, B and myeloid cells. The engagement of PD-1 with its two ligands, PD-L1 and PD-L2, inhibits proliferation of T cell and production of a series of its cytokines. The blockade of PD-1 pathway is involved in antiviral and antitumoral immunity. In this study, human PD-1 cDNA encoding extracellular domain was amplified and cloned into expression plasmid pGEX-5x-3. The fusion protein GST-PD-1 was effectively expressed in E. coli BL21 (DE3) as inclusion bodies and a denaturation and refolding procedure was performed to obtain bioactive soluble GST-PD-1. Fusion protein of above 95% purity was acquired by a convenient two-step purification using GST affinity and size exclusion columns. Furthermore, a PD-L1-dependent in vitro bioassay method was set up to characterize GST-PD-1 bioactivity. The results suggested that GST-PD-1 could competently block the interaction between PD-L1 and PD-1 and increase the production of IL-2 and IFN-gamma of phytohemagglutinin-activated T cells.


Subject(s)
Antigens, Surface/chemistry , Escherichia coli/metabolism , Glutathione Transferase/chemistry , Recombinant Fusion Proteins/chemistry , Animals , Antigens, CD , Apoptosis Regulatory Proteins , Biological Assay , Blotting, Western , CD28 Antigens/metabolism , Cell Line , Cloning, Molecular , Cytokines/metabolism , DNA, Complementary/metabolism , Electrophoresis, Polyacrylamide Gel , Genetic Vectors , Glutathione Transferase/metabolism , Humans , Interferon-gamma/metabolism , Interleukin-2/metabolism , Ligands , Mice , Phytohemagglutinins/pharmacology , Plasmids/metabolism , Programmed Cell Death 1 Receptor , Protein Folding , Recombinant Fusion Proteins/metabolism , T-Lymphocytes/metabolism , Time Factors , Transfection
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