EXPERIMENTS IN FLUIDS
·
2024
·Vol. 65
·期 9
·1-12
·
IF 2.3
Ulrich Hannah,Weiß Richard,Zigan Lars
This work shows new insights on the application of two-color laser-induced-fluorescence (2c-LIF) thermometry in a droplet chain. A two-dye mixture is used in ethanol, water and ethanol/water mixtures in order to reach a high-temperature sensitivity and avoid the detection of lasing effects in the droplets. Various droplet sizes are recorded in regard to the limitation of the detection system for very small micrometric droplets. The breakup of a droplet chain is measured to assess the spectral detection system in applications with liquid structures of different sizes. Additionally, a proposal to expand the 2c-LIF application for studying ethanol/water droplets regarding mixture composition with a third color channel is presented. Forming two intensity ratios, the spectra can be used to obtain information on the mixture composition of the solvent. Measurements in different ethanol/water mixtures containing 0–100 vol% water are evaluated to show this possibility.
✓ 已验证
DOI
高影响因子
Nature Communications
·
2022
·Vol. 13
·期 1
·1-9
·
IF 17.694
Gao Haowen,Ai Xin,Wang Hongchun,Li Wangqin,Wei Ping,Cheng Yong,Gui Siwei,Yang Hui,Yang Yong,Wang Ming-Sheng
Solid electrolytes hold the promise for enabling high-performance lithium (Li) metal batteries, but suffer from Li-filament penetration issues. The mechanism of this rate-dependent failure, especially the impact of the electrochemo-mechanical attack from Li deposition, remains elusive. Herein, we reveal the Li deposition dynamics and associated failure mechanism of solid electrolyte by visualizing the Li|Li 7 La 3 Zr 2 O 12 (LLZO) interface evolution via in situ transmission electron microscopy (TEM). Under a strong mechanical constraint and low charging rate, the Li-deposition-induced stress enables the single-crystal Li to laterally expand on LLZO. However, upon Li “eruption”, the rapidly built-up local stress, reaching at least GPa level, can even crack single-crystal LLZO particles without apparent defects. In comparison, Li vertical growth by weakening the mechanical constraint can boost the local current density up to A·cm −2 level without damaging LLZO. Our results demonstrate that the crack initiation at the Li|LLZO interface depends strongly on not only the local current density but also the way and efficiency of mass/stress release. Finally, potential strategies enabling fast Li transport and stress relaxation at the interface are proposed for promoting the rate capability of solid electrolytes.
✓ 已验证
DOI
高影响因子
COLLOID AND POLYMER SCIENCE
·
2024
·
IF 2.2
Zhao Dan,Yang Weili,Shen Guanglite,Zhang Wenhui,Feng Huixia
Phenol–formaldehyde resin can be used to improve oil recovery; its key lies in its aggregation behavior and blocking strength. However, the traditional phenol–formaldehyde resin used in the petroleum field is all prepared by phenol and formaldehyde. In order to get rid of the dependence on fossil resources and make full use of renewable biomass resources, we used the abandoned walnut shells of the unique agricultural and forestry crops in Gansu province, which contains lignin partially replaced phenol to synthesize the new sulfonated lignin-based phenol–formaldehyde resin (SLPFR). The results showed that the optimum conditions for microwave polymers were polystyrene substitution rate of 20 wt%, decomposition temperature of 160 ℃, decommissioning time of 20 min, and sodium hydroxide concentration of 0.3 mol/L. Infrared spectroscopes and scanning telescopes have shown that after disintegration, there was an increased concentration of phosphorus, which had more active spots and was more suitable for replacing phenylphenol-synthetic formaldehyde resins. LC–MS indicated the molecular mass of SLPFR and the possible structure of molecules, indicating the successful synthesis of SLPFR. In this work, the aggregation behavior and dispersion stability of SLPFR were investigated from the composition of formation water. The effects of metal cations (Na + , Mg 2+ , Ca 2+ ) on the dispersion stability of SLPFR in formation water were determined by turbidimetry, and the effects of metal cations on the particle size and zeta potential of the SLPFR system were measured by dynamic light scattering method and electrophoretic light scattering method. The stability of the aggregate structure of the SLPFR system was calculated by combining the fractal dimension. In this paper, the surfactant + SLPFR system and partially hydrolyzed polyacrylamide (HPAM) + SLPFR system were designed for the specific conditions of oil reservoirs, and the effects of metal cations on the aggregation behavior and dispersion stability of these two systems were studied. Based on the above comprehensive analysis, aggregation models were constructed to describe the aggregation behavior and dispersion stability of the HPAM + surfactant + SLPFR system. This makes it possible to predict in real time the migration and plugging of SLPFR aggregates in formation water. Graphical abstract
✓ 已验证
产品关联
DOI
高影响因子
Journal of Neuroinflammation
·
2025
·Vol. 22
·期 1
·1-20
·
IF 10.1
Hong Wenxiang,Ma Hongbo,Li Zhibin,Du Yiwen,Xia Wenjing,Yin Han,Huang Han,Sun Zebing,Gai Renhua,Tong Lexian,Zhu Hong,Wang Jincheng,Yang Bo,He Qiaojun,Weng Qinjie,Wang Jiajia
The epigenetic modification of histone H3 lysine 27 trimethylation (H3K27me3) by the embryonic ectoderm development (EED) protein is closely associated with the regulation of transcriptional programs and is implicated in autoimmune diseases. However, the efficacy of targeting H3K27me3 for the treatment of neuroinflammation remains unclear. In this study, we demonstrate that systemic administration of an EED inhibitor diminishes the inflammatory response mediated by dendritic cells (DCs), thereby alleviating experimental autoimmune encephalitis (EAE), a representative mouse model of autoimmune diseases in the central nervous system (CNS). Our findings indicate that EED inhibitors suppress DC migration by upregulating genes in the WNT signaling pathway that are epigenetically marked by H3K27me3. Conversely, inhibiting the WNT pathway partially reverses the impaired DC migration caused by EED inhibitors. Additionally, the genetic deletion of Eed inhibits DC migration and effectively mitigates autoimmune symptoms and inflammatory infiltration into the CNS in EAE. These results highlight EED as a critical regulator of DC migration and suggest its potential as a therapeutic target for autoimmune disorders.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
·
2022
·Vol. 106
·期 7
·2703-2714
·
IF 5.56
Geng Rui,Sun Yaning,Li Rui,Yang Jifei,Ma Hongfang,Qiao Zixuan,Lu Qingxia,Qiao Songlin,Zhang Gaiping
Abstract African swine fever virus (ASFV) causes a highly contagious and often lethal swine viral disease, and leads to tremendous economic losses to the swine industry. Unfortunately, there are no vaccines and effective antiviral agents available to prevent and control ASFV outbreaks. Therefore, it is necessary to develop simple and rapid strategies to monitor ASFV-infected pigs to restrain its spread. In the current study, ASFV capsid protein p72 was expressed along with its chaperone pB602L to form trimers in human embryonic kidney 293 (HEK293) cells. The p72 trimers were subsequently labeled with colloidal gold to develop a immunochromatographic strip. The strip showed high specificity to ASFV-positive serum and no cross-reactivity to other swine virus positive sera. Importantly, the strip showed a higher sensitivity of detecting ASFV antibodies in both positive standard serum and clinical serum samples than a commercial enzyme-linked immunosorbent assay (ELISA) kit. Taken together, these results demonstrate the strip as a reliable diagnostic tool against ASFV infection, which will be appropriate for application in prevention and control of ASFV.
Key points
• ASFV p72 trimers were successfully generated . • A colloidal gold strip was developed based on ASFV p72 trimers . • The strip is appropriate for detecting ASFV antibodies in the field .
✓ 已验证
DOI
PubMed
高影响因子
JOURNAL OF NANOBIOTECHNOLOGY
·
2022
·Vol. 20
·期 1
·1-19
·
IF 9.429
Liu Mengyao,Li Yonghong,Xing Wei,Zhang Yuqin,Xie Xi,Pang Jiadong,Zhou Fangjian,Yang Jiang
Background Effective and accurate screening of oncological biomarkers in peripheral blood circulation plays an increasingly vital role in diagnosis and prognosis. High-sensitivity assays can effectively aid clinical decision-making and intervene in cancer in a localized status before they metastasize and become unmanageable. Meanwhile, it is equally pivotal to prevent overdiagnosis of non-life-threatening cancer by eliminating unnecessary treatment and repeated blood draws. Unfortunately, current clinical screening methodologies can hardly simultaneously attain sufficient sensitivity and specificity, especially under resource-restrained circumstances. To circumvent such limitations, particularly for cancer biomarkers from early-onset and recurrence, we aim to develop a universal plasmonic platform for clinical applications, which macroscopically amplifies multiplexed fluorescence signals in a broad spectral window and readily adapts to current assay setups without sophisticated accessories or expertise at low cost.Methods The plasmonic substrate was chemically synthesized in situ at the solid–liquid interface by rationally screening a panel of reducing monosaccharides and tuning the redox reactions at various catalyst densities and precursor concentrations. The redox properties were studied by Benedict’s assay and electrochemistry. We systemically characterized the morphologies and optical properties of the engineered plasmonic Ag structures by scanning electron microscopy (SEM) and spectroscopy. The structure-fluorescence enhancement correlation was explicitly explained by the finite-difference time-domain (FDTD) simulation and a computational model for gap distribution. Next, we established an enhanced fluoroimmunoassay (eFIA) using a model biomarker for prostate cancer (PCa) and validated it in healthy and PCa cohorts. Prognosis was explored in patients subject to surgical and hormonal interventions following recommended PCa guidelines.Results The monosaccharide-mediated redox reaction yielded a broad category of Ag structures, including sparsely dispersed nanoparticles (NPs) of various sizes, semi-continuous nanoislands, and crackless continuous films. Optimal broad-spectral fluorescence enhancement from green to far-red was observed for the inhomogeneous, irregularly-shaped semi-continuous Ag nanoisland substrate (AgNIS), synthesized from a well-balanced redox reaction at a stable rate mediated by mannose. In addition, different local electric field intensity distributions in response to various incident excitations were observed at the nanoscale, elucidating the need for irregular and inhomogeneous structures. AgNIS enabled a maximized 54.7-fold macroscopically amplified fluorescence and long-lasting photostability. Point-of-care availability was fulfilled using a customized smartphone prototype with well-paired optics. The eFIA effectively detected the PCa marker in cell lines, xenograft tumors, and patient sera. The plasmonic platform rendered a diagnostic sensitivity of 86.0% and a specificity of 94.7% and capably staged high-grade PCa that the clinical gold standard test failed to stratify. Patient prognosis of robotic-assisted surgeries and hormone therapies was non-invasively monitored following efficient medical interventions. The assay time was significantly curtailed on the plasmonic platform upon microwave irradiation.Conclusion sBy investigating the effects of reducing monosaccharides on the seed-mediated chemical synthesis of plasmonic Ag structures, we deduced that potent multiplexed fluorescence enhancement originated from both an adequate reducing power and a steady reduction rate. Furthermore, the inhomogeneous structure with adequate medium gap distances afforded optimal multiwavelength fluorescence enhancement, thus empowering an effective eFIA for PCa. The clinically validated diagnostic and prognostic features, along with the low sample volume, point-of-care feasibility with a smartphone, and microwave-shortened assay time, warrant its potential clinical translation for widespread cancer biomarker analysis.Graphical Abstract
✓ 已验证
DOI
PubMed
高影响因子
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
·
2022
·Vol. 106
·期 23
·7805-7817
·
IF 5.56
Fu Linglong,Sun Mengning,Wen Weizhang,Dong Na,Li Defa
Abstract Small ubiquitin-like modifier (SUMO) tag is widely used to promote soluble expression of exogenous proteins, which can then be cleaved by ubiquitin-like protease 1 (Ulp1) to obtain interested protein. But the application of Ulp1 in large-scale recombinant protein production is limited by complicated purification procedures and high cost. In this study, we describe an efficient and simple method of extracellular production of Ulp1 403-621 using a leaky Escherichia coli BL21(DE3), engineered by deleting the peptidoglycan-associated outer membrane lipoprotein ( pal ) gene. Ulp1 403-621 was successfully leaked into extracellular supernatant by the BL21(DE3)-Δ pal strain after IPTG induction. The addition of 1% glycine increased the extracellular production of Ulp1 403-621 approximately four fold. Moreover, extracellular Ulp1 403-621 without purification had high activities for cleaving SUMO fusion proteins, and antimicrobial peptide pBD2 obtained after cleavage can inhibit the growth of Staphylococcus aureus . The specific activity of extracellular Ulp1 403-621 containing 1 mM EDTA and 8 mM DTT reached 2.0 × 10 6 U/L. Another commonly used protease, human rhinovirus 3C protease, was also successfully secreted by leaky E. coli strains. In conclusion, extracellular production of tool enzymes is an attractive way for producing large-scale active recombinant proteins at a lower cost for pharmaceutical, industrial, and biotechnological applications. Key points
• First report of extracellular production of Ulp1
403-621
in leaky Escherichia coli BL21(DE3) strain.
• One percent glycine addition into cultivation medium increased the extracellular production of Ulp1
403-621
approximately four fold.
• The specific activity of extracellular Ulp1
403-621
produced in this study reached 2.0 × 10
6
U/L.
✓ 已验证
DOI
PubMed
高影响因子
LABORATORY INVESTIGATION
·
2019
·Vol. 100
·期 3
·378-386
·
IF 3.684
Lang Ping-Ping,Bai Jie,Zhang Yun-Long,Yang Xiao-Lei,Xia Yun-Long,Lin Qiu-Yue,Li Hui-Hua
Monocyte and adhesion infiltration into the arterial subendothelium are initial steps in hypertension development. The endothelial intercellular adhesion molecule-1 (ICAM-1) has been implicated in the recruitment and adhesion of leukocytes in several cardiac diseases. However, the role of ICAM-1 in angiotensin II (Ang II)-induced hypertension development remains unknown. Hypertension was induced by administering an infusion of Ang II (1000 ng/kg/min) to wild-type (WT) mice treated with an IgG control or ICAM-1 neutralizing antibody (1 and 2 mg/mouse/day, respectively). Blood pressure was determined using the tail-cuff system. Vascular remodeling was assessed by performing a histological examination. Inflammation and reactive oxygen species (ROS) levels were determined by using immunostaining. Vascular dysfunction was assessed by aortic ring assay. The expression of fibrotic markers, cytokines and NOX was evaluated by quantitative real-time PCR analysis. Our results demonstrate that Ang II infusion markedly increased the ICAM-1 level in the aorta. Blocking ICAM-1 with a neutralizing antibody significantly attenuated Ang II-induced arterial hypertension, vascular hypertrophy, fibrosis, macrophage infiltration, and ROS production and improved vascular relaxation. In conclusion, ICAM-1-mediated monocyte adhesion and migration play a critical role in Ang II-induced arterial hypertension and vascular dysfunction. ICAM-1 inhibitors may represent a new therapeutic strategy for the treatment of this disease.
✓ 已验证
DOI
PubMed
高影响因子
MICROCHIMICA ACTA
·
2017
·Vol. 184
·期 9
·3487-3496
·
IF 4.58
Sun Duanping,Lu Jing,Wang Xiangyan,Zhang Yuanqing,Chen Zuanguang
The authors describe a method for the detection and determination of human liver cancer cells in blood. The cytosensing system consists of a microfabricated chip-based electrochemical aptasensor that contains multifunctional hybrid electrochemical nanoprobes and an indium tin oxide (ITO) electrode array interface functionalized with cell-targeting aptamer and gold nanoparticles (AuNPs). The thiolated cell targeting aptamer (referred to as TLS11a) was immobilized on the ITO electrode/AuNPs for specific adhesion of hepatocellular carcinoma cells (HepG2). The hybrid nanoprobe system consists of hydroquinone (HQ) as an electrochemical probe, horseradish peroxidase (HRP), and an aptamer/hemin/G-quadruplex aggregate that was immobilized on gold/palladium-functionalized ZnO nanorods (ZnO@Au-Pd). The nanoprobes are capable of amplifying the voltammetric signal and capturing the target cells. Best operated at around −90 mV (vs Ag/AgCl), the electrode has a linear response that covers the 10^2 to 10^7 HepG2 cells per mL concentration range, with a 10 cell per mL detection limit. Captured cells may be released from the electrode via electrochemical desorption to break the Au-S bonds.
Schematic of an indium tin oxide (ITO) electrode array-based electrochemical aptamer cytosensor for the specific capture, sensitive detection and controlled release of HepG2 cancer cells. AuNP: gold nanoparticle; HQ: hydroquinone; HRP: horseradish peroxidase.
✓ 已验证
DOI
高影响因子
MICROCHIMICA ACTA
·
2021
·Vol. 188
·期 5
·1-9
·
IF 5.833
Wu Mingmin,Zhang Mengtian,Fan Zhiwei,Qin Xinyue,Zhu Xiaoxia,Ji Haiwei,Qin Yuling,Wang Qi,Wu Li
Sensitive and accurate detection of DNA methyltransferase (MTase) is conducive to the understanding of the fundamental biological processes related to DNA methylation, clinical disease diagnosis, and drug discovery. Herein, a new fluorescence transducer based on Förster resonance energy transfer (FRET) between the donor upconversion nanoparticles (UCNPs) and the efficient acceptor gold nanorods (AuNRs) for MTase activity analysis and its inhibitor screening is presented. A double-strand DNA linker between UCNPs and AuNRs could be digested by restriction endonuclease Hha I, preventing the FRET process and recovering the upconversion luminescence (UCL) intensity. With the treatment of MTase, the cutting site was disturbed by the methylation of cytosine, blocking the enzyme digestion. The transducer presented here showed an excellent analytical performance toward MTase M. Hha I in the concentration range 0.08~24 U mL −1 with a detection limit of 0.057 U mL −1 calculated according to the UCL intensity changes at 656 nm excited by 980 nm CW laser, which is superior to most of the reported methods. Furthermore, the as-fabricated transducer also demonstrated high testing and screening capability toward enzyme inhibitors’ evaluation. The method takes the advantage of low background fluorescence of UCNPs to improve the accuracy of the measurement, which can be developed as a general strategy for the analysis of various disease-related methyltransferase activity and their corresponding inhibitors, offering a promising strategy for high-performance diagnosis, high-efficient drug exploitation, and treatment effectiveness evaluation. Graphical abstract
✓ 已验证
DOI
PubMed
高影响因子
Biotechnology for Biofuels
·
2019
·Vol. 12
·期 1
·1-18
·
IF 5.452
Yi Xia,Gao Qiuqiang,Zhang Lei,Wang Xia,He Yanqing,Hu Fengxian,Zhang Jian,Zou Gen,Yang Shihui,Zhou Zhihua,Bao Jie
Background Fast, complete, and ultimate removal of inhibitory compounds derived from lignocellulose pretreatment is the prerequisite for efficient production of cellulosic ethanol and biochemicals. Biodetoxification is the most promising method for inhibitor removal by its unique advantages. The biodetoxification mechanisms of a unique diploid fungus responsible for highly efficient biodetoxification in solid-state culture was extensively investigated in the aspects of cellular structure, genome sequencing, transcriptome analysis, and practical biodetoxification.Results The inborn heterozygous diploid structure of A. resinae ZN1 uniquely contributed to the enhancement of inhibitor tolerance and conversion. The co-expression of gene pairs contributed to the enhancement of the degradation of lignocellulose-derived model inhibitors. The ultimate inhibitors degradation pathways and sugar conservation were elucidated by microbial degradation experimentation as well as the genomic and transcriptomic sequencing analysis.Conclusion sThe finding of the heterozygous diploid structure in A. resinae ZN1 on biodetoxification took the first insight into the global overview of biodetoxification mechanism of lignocellulose-derived inhibitors. This study provided a unique and practical biodetoxification biocatalyst of inhibitor compounds for lignocellulose biorefinery processing, as well as the synthetic biology tools on biodetoxification of biorefinery fermenting strains.
✓ 已验证
DOI
PubMed
高影响因子
Bioresources and Bioprocessing
·
2022
·Vol. 9
·期 1
·1-9
·
IF 4.983
Ma Yue,Li Tianzhen,Tan Zijian,Ma Long,Liu Haifeng,Zhu Leilei
Catalytic valorization of raw glycerol derived from biodiesel into high-value chemicals has attracted great attention. Here, we report chemoenzymatic cascade reactions that convert glycerol to lactic acid and glycolic acid. In the enzymatic step, a coenzyme recycling system was developed to convert glycerol into 1,3-dihydroxyacetone (DHA) with a yield of 92.3% in potassium phosphate buffer (300 mM, pH 7.1) containing 100 mM glycerol, 2 mM NAD + , 242 U/mL glycerol dehydrogenase-GldA and NADH oxidase-SpNox K184R at 30 °C. Subsequently, NaOH or NaClO 2 catalyzes the formation of lactic acid and glycolic acid from DHA. The high yield of lactic acid (72.3%) and glycolic acid (78.2%) verify the benefit of the chemoenzymatic approaches. Graphical Abstract
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）