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Combined fluorescence and electrochemical investigation on the binding interaction between organic acid and human serum albumin

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Journal of environmental Sciences 2009年第3期21卷 373-379页

作者： CHEN Yan-Min,guo liang-hong state key laboratory of environmental chemistry and ecotoxicology,Research Center for Eco-environmental Sciences,Chinese Academy of Sciences,Beijing 100085,China. state key laboratory of environmental chemistry and ecotoxicology Research Center for Eco-environmental Sciences Chinese Academy of Sciences Beijing 100085 China

Human serum albumin （HSA） is a plasma protein responsible for the binding and transport of fatty acids and a variety of exogenous chemicals such as drugs and environmental pollutants. Such binding plays a crucial role in determining the ADME （absorption, distribution, metabolism, and excretion） and bioavailability of the pollutants. The binding interaction between HSA and acetic acid （C2）, octanoic acid （C8） and dodecanoic acid （C12） has been investigated by the combination of site-specific fluorescent probe, tryptophan intrinsic fluorescence and tyrosine electrochemistry. For the study of the fatty acid interaction with the two drug-binding sites on HSA, two fluorescent probes, dansylamide and dansyl-L-proline were employed in the displacement measurements. Intrinsic fluorescence of tryptophan in HSA was monitored upon addition of the fatty acids into HSA. Electrocatalyzed response of the tyrosine residues in HSA by a redox mediator was used to investigate the binding interaction. Qualitatively, observations from these three approaches were very similar. HSA did not show any change in the fluorescence and electrochemical experiments after mixing with C2, suggesting there is no significant interaction with the short-chain fatty acid. For C8, the measured signal dropped in a single-exponential mode, indicating an independent and non-cooperative binding. The calculated association constant and binding ratio were 3.1 × 10^6 L/mol and 1 with drug binding Site Ⅰ, 1.1 × 107 L/mol and 1 with Site Ⅱ, and 7.0× 0^4 L/mol and 4 with the tryptophan site, respectively. The measurements with C12 displayed multiple phases of fluorescence change, suggesting cooperativity and allosteric effect of the C12 binding. These results correlate well with those obtained by the established methods, and validate the new approach as a viable tool to study the interactions of environmental pollutants with biological molecules.

关键词： absorption, distribution, metabolism, and excretion (ADME) organic acid human serum albumin fluorescence electrochemistry

“Co-coordination force”assisted rigid-flexible coupling crystalline polymer for high-performance aqueous zinc-organic batteries

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Chinese Chemical Letters 2024年第9期35卷 501-506页

作者： Jun guo Zhenbang Zhuang Wanqiang Liu Gang huang School of Materials Science and Engineering Changchun University of Science and TechnologyChangchun 130022China state key laboratory of Rare Earth Resource Utilization Changchun Institute of Applied ChemistryChinese Academy of SciencesChangchun 130022China key laboratory of Automobile Materials Ministry of EducationDepartment of Materials Science and EngineeringJilin UniversityChangchun 130022China

Organic electrode materials(OEMs)have attracted substantial attention for aqueous zinc-ion batteries(AZIBs)due to their advantages in relieving resource and environmental ***,the potential of OEMs is plagued by their low achievable capacity and high ***,we have proposed a new concept of“co-coordination force”and designed a rigid-flexible coupling crystalline polymer that can overcome the abovementioned *** obtained crystalline polymer(BQSPNs)with multiredox centres makes the BQSPNs exist intermolecular hydrogen bonds(HB)among-C=O,-C=N,and-NH and consequently exhibits transverse two-dimensional arrays and longitudinalπ-πstacking ***,in-situ FTIR,Raman,variable temperature FTIR spectra,and 2D nuclear overhauser effect spectroscopy(NOESY)well capture the existence and evolution process of HB during the electrochemistry reaction process of BQSPNs,uncovering the effect of HB in stabilizing the structure and promoting the reaction *** a result,the BQSPNs with rationally designed“co-coordination force”deliver a high capacity of 459.6 m Ah/g and a stable cycling lifetime for more than 100,000 cycles at 10 A/g in *** results disclose the HB effect and provide a brand-new strategy for high-performance OEMs design.

关键词： Co-coordination force Crystalline polymer Hydrogen bonds Organic electrode materials Aqueous zinc-ion batteries

Effects of maize root exudates and organic acids on the desorption of phenanthrene from soils

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Journal of environmental Sciences 2009年第7期21卷 920-926页

作者： ZHU Yanhong, ZHANG Shuzhen, huang honglin, WEN Bei state key laboratory of environmental chemistry and ecotoxicology, Research Center for Eco-environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China. state key laboratory of environmental chemistry and ecotoxicology Research Center for Eco-Environmental Sciences Chinese Academy of Sciences Beijing 100085 China

The effects of maize root exudates and low-molecular-weight-organic anions （LMWOAs） on the desorption of phenanthrene from eight artificially contaminated soils were evaluated. A significant negative correlation was observed between the amounts of phenanthrene desorbed and the soil organic carbon （SOC） contents （P 〈 0.01）, and the influences of soil pH and clay content on phenanthrene desorption were insignificant （P 〉 0.1）. Neither maize root exudates nor oxalate and citrate anions influenced desorption of phenanthrene with the addition of NaN3. A faster phenanthrene desorption occurred without the addition of NaN3 in the presence of maize root exudates than oxalate or citrate due to the enhanced degradation by root exudates. Without the addition of NAN3, oxalate or citrate at different concentrations could inhibit phenanthrene desorption to different extents and the inhibiting effect by citrate was more significant than by oxalate. This study leads to the conclusion that maize root exudates can not enhance the desorption under abiotic condition with the addition of NaN3 and can promote the desorption of phenanthrene in soils without the addition of NaN3.

关键词： phenanthrene desorption low-molecular-weight-organic anions (LMWOAs) root exudates soils

Levels and distributions of polychlorinated biphenyls in sewage sludge of urban wastewater treatment plants

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Journal of environmental Sciences 2009年第4期21卷 468-473页

作者： guo Li, ZHANG Bing, XIAO Ke, ZHANG Qinghua, ZHENG Minghui state key laboratory of environmental chemistry and ecotoxicology, Research Center for Eco-environmental Sciences, Chinese Academy of Sciences,Beijing 100085, China state key laboratory of environmental chemistry and ecotoxicology Research Center for Eco-Environmental Sciences Chinese Academy of Sciences Beijing 100085 China

Concentrations of polychlorinated biphenyls （PCBs） have been measured in sewage sludge samples from 8 urban wastewater treatment plants in Beijing, China. The PCB congeners were analyzed by isotope dilution high resolution gas chromatography/high resolution mass spectrometry method. The concentration of PCBs ranged from 65.6 to 157 ng/g dry weight （dw）, with a mean value of 101 ng/g dw. The dioxin-like PCB WHO-TEQs （World Health Organization-Toxic Equivalents） of the sludge were lower than 1 pg /g dw. Consequently, all the concentrations of PCBs in sludge samples were below the upper limit for land application according to the Chinese legislation law for agriculture use. The PCB homologue profiles in sludge samples were dominated by tri-CBs and tetra- CBs. Similar distributions have been found in one of the Chinese PCB commercial products. The patterns of dioxin-like and indicator congeners observed in this study were quite similar in all samples. The predominant congener for dioxin-like and indicator PCBs were PCB-118 and PCB-28, respectively, while PCB-126 had the highest TEQ value.

关键词： polychlorinated biphenyls wastewater treatment plant sewage sludge distribution

Surface engineering of P2-type cathode material targeting long-cycling and high-rate sodium-ion batteries

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Journal of Energy chemistry 2024年第10期97卷 444-452,I0009页

作者： Jun Xiao Yang Xiao Shijian Wang Zefu huang Jiayi Li Cheng Gong Guilai Zhang Bing Sun hong Gao Huiqiao Li Xin guo Yong Wang Hao Liu guoxiu Wang Centre for Clean Energy Technology School of Mathematical and Physical SciencesFaculty of ScienceUniversity of Technology SydneyBroadwaySydneyNew South Wales 2007Australia Joint International laboratory on environmental and Energy Frontier Materials School of Environmental and Chemical EngineeringShanghai UniversityShanghai 200444China state key laboratory of Materials Processing and Die and Mould Technology School of Materials Science and EngineeringHuazhong University of Science and TechnologyWuhan 430074HubeiChina

The widespread interest in layered P2-type Mn-based cathode materials for sodium-ion batteries(SIBs)stems from their cost-effectiveness and abundant ***,the inferior cycle stability and mediocre rate performance impede their further development in practical ***,we devised a wet chemical precipitation method to deposit an amorphous aluminum phosphate(AlPO_(4),denoted as AP)protective layer onto the surface of P2-type Na_(0.55)Ni_(0.1)Co_(0.7)Mn_(0.8)O_(2)(NCM@AP).The resulting NCM@5AP electrode,with a 5 wt%coating,exhibits extended cycle life(capacity retention of78.4%after 200 cycles at 100 mA g^(-1))and superior rate performance(98 mA h g^(-1)at 500 mA g^(-1))compared to pristine ***,our investigation provides comprehensive insights into the phase stability and active Na^(+)ion kinetics in the NCM@5AP composite electrode,shedding light on the underlying mechanisms responsible for the enhanced performance observed in the coated electrode.

关键词： Layered metal oxides Sodium-ion batteries P2-type structure Surface engineering

Detection of Peptide Damage Induced by Fenton Reaction with Electrochemical Biosensor

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生物物理学报 2009年第S1期25卷 400-401页

作者： Na Qu, liang-hong guo and Ben-Zhan Zhu state key laboratory of environmental chemistry and ecotoxicology, Research Center for Eco-environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.

Hydroxyl radical is one of the most reactive oxygen species (ROS) in biological systems, which can react with proteins and result in protein oxidation and damage. Oxidative

关键词： Electrochemical Biosensor Peptide Damage Fenton Reaction Hydroxyl radical

A zincophilic molecular brush for a dendrite-free,corrosionresistant,zinc metal anode with a long life cycle

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Nano Research 2024年第1期17卷 390-396页

作者： Penggao Liu Jia guo Xinyue Chen Ting Wang Yanping huang Shasha Gao Tao Wang Dongling Wu Kaiyu Liu state key laboratory of chemistry and Utilization of Carbon based Energy Resources College of ChemistryXinjiang UniversityUrumqi 830017China Hunan Provincial key laboratory of Chemical Power Sources College of Chemistry and Chemical EngineeringCentral South UniversityChangsha 410083China key laboratory of New Low-carbon Green Chemical Technology School of Chemistry and Chemical EngineeringEducation Department of Guangxi Zhuang Autonomous RegionGuangxi UniversityNanning 530004China key laboratory of Microelectronics and Energy of Henan Province Department of Physics and Electronic EngineeringXinyang Normal UniversityXinyang 464000China Interdisciplinary Research Center for Sustainable Energy Science and Engineering(IRC4SE2) School of Chemical EngineeringZhengzhou UniversityZhengzhou 450001China

Zinc-based aqueous rechargeable batteries have attracted extensive attention due to their low cost,safety,and environmental ***,dendrite growth and hydrogen evolution of Zn anodes limit their large-scale application.A new strategy to produce a polyacrylamide/reduced graphene oxide(PAM@rGO)molecular nanobrush coating and control Zn electrolyte interface engineering is proposed for use in highly reversible Zn plating/*** evolution is inhibited,and Zn deposition is consolidated using the rich zincophilic functional groups of the branched polyacrylamide chain and the high conductivity of *** to the synergistic effects of corrosion resistance and dendrite-free growth,PAM@rGO/Zn provides prolonged and reversible Zn plating/*** functional theory(DFT)calculations expand on homogenized *** PAM@rGO/Zn||activated carbon(AC)capacitor exhibits long cyclic stability,fast ion transfer,and minimal interfacial *** study provides experimental and theoretical bases for the structural design of Zn anode.

关键词： zincophilic nanobrush polyacrylamide/reduced graphene oxide(PAM@rGO)/Zn surface modification Zn based energy storage

One-step and high-density protein immobilization on epoxysilane-modified silica nanoparticles

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Chinese Science Bulletin 2009年第15期54卷 2620-2626页

作者： ZHANG Qin huang rongfu guo liang-hong state key laboratory of environmental chemistry and ecotoxicology Research Center for Eco-environmental Sciences ChineseAcademy of Sciences Beijing 100085 China

Silica nanoparticles are most commonly modified with amino-silanes, followed by post-modification activation for protein immobilization. In this work, epoxy-functionalized silica nanoparticles were prepared by modification with glycidyloxypropyl trimethoxysilane (GPTMS) for direct protein immobilization. Silica nanoparticles possessed an average size of 46 nm, but increased to 63 nm after GPTMS modification. Reaction time, reaction temperature and GPTMS content had no significant effect on particle size. Zeta potential of SiO2 changed from ?26mV to +38mV after modification. Fourier-transformed infrared spectroscopy revealed alkyl C-H bending and stretching bands at 2944 cm-1, 1343 cm-1 and 1465 cm-1, respectively, for the modified nanoparticles. Fluorescein cadaverine was found to bind to GPTMS-modified SiO2, but not to bare SiO2, indicating the chemical reactivity of epoxy groups on the modified nanoparticle with amines. Finally, fluorescently labeled bovine serum albumin (BSA) was used as a model protein to investigate the capacity of epoxy-SiO2 nanoparticles for protein immobilization. The results showed that more proteins were immobilized on the particle with longer reaction time, higher NaCl concentration, lower pH, and less GPTMS content. More importantly, proteins bound to epoxy-SiO2 nanoparticle were highly stable. Under optimized reaction conditions, as much as 25 mg BSA/g nanoparticle was covalently attached to the nanoparticle. The epoxy silane modification of silica nanoparticles offers a reactive surface for one-step and high-density protein immobilization.

关键词：二氧化硅制备方法反应条件纳米粒子

Emerging strategies and developments in oxygen reduction reaction using high-performance platinum-based electrocatalysts

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Nano Research 2024年第5期17卷 3516-3532页

作者： Asad Ali Aatto Laaksonen guo huang Shahid Hussain Shuiping Luo Wen Chen Pei Kang Shen Jinliang Zhu Xiaoyan Ji Energy Engineering Division of Energy ScienceLuleåUniversity of Technology97187 LuleåSweden Department of Materials and environmental chemistry Arrhenius LaboratoryStockholm UniversitySE-10691 StockholmSweden Center of Advanced Research in Bionanoconjugates and Biopolymers “Petru Poni”Institute of Macromolecular ChemistryIasi 700469Romania state key laboratory of Materials-Oriented and Chemical Engineering Nanjing Tech UniversityNanjing 211816China College of Materials Science and Engineering Shenzhen UniversityShenzhen 518060China School of Resources Environment and MaterialsState Key Laboratory of Processing for Non-ferrous Metal and Featured MaterialsGuangxi UniversityNanning 530004China

The global practical implementation of proton exchange membrane fuel cells(PEMFCs)heavily relies on the advancement of highly effective platinum(Pt)-based electrocatalysts for the oxygen reduction reaction(ORR).To achieve high ORR performance,electrocatalysts with highly accessible reactive surfaces are needed to promote the uncovering of active positions for easy mass *** this critical review,we introduce different approaches for the emerging development of effective ORR electrocatalysts,which offer high activity and *** strategies,including morphological engineering,geometric configuration modification via supporting materials,alloys regulation,core-shell,and confinement engineering of single atom electrocatalysts(SAEs),are discussed in line with the goals and requirements of ORR performance *** review the ongoing development of Pt electrocatalysts based on the syntheses,nanoarchitecture,electrochemical performances,and *** eventually explore the obstacles and research directions on further developing more effective electrocatalysts.

关键词： oxygen reduction reaction(ORR) Pt-based electrocatalysts proton exchange membrane fuel cells(PEMFCs) morphology and alloys strategies single atom electrocatalysts(SAEs)