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A New Colorimetric Sensor for Cysteine Determination Based on Dual Reacting-mediated Strategy
Honghong Rao,Ying Li,Guoliang Zhang,Zhonghua Xue,Guohu Zhao,Shengyin Li,Xinzhen Du 대한화학회 2017 Bulletin of the Korean Chemical Society Vol.38 No.9
Rapid and simple determination of cysteine is a key requirement for both diagnosis and treatment of diseases. A novel concept is proposed for combining dual reacting-mediated process into the construction of a simple yet effective colorimetric strategy for cysteine detecting, which is based on the analyte-induced formation of ferrous ion and graphene oxide-supported ionic recognition through selective coordination process between phenanthroline molecule and ferrous ion. In colorimetric analysis, the simple principle of ferrous ion that cysteine-induced can be recognized by phenanthroline indicator due to their good binding affinity and therefore provided a sensitive optical readout for conveniently detecting cysteine. Proof-concept experiments demonstrate that the proposed colorimetric system shows rapid response toward cysteine determination as well as with a satisfying detection limit of 4.8 μM only by using simple UV–Vis spectroscopy and 15 μM with the naked eye.
Hansong Xue,Weina Zhang,Xinyu Li,Xiaochang You,Jinsong Rao,Fusheng Pan 대한금속·재료학회 2017 ELECTRONIC MATERIALS LETTERS Vol.13 No.3
Samarium oxide (Sm2O3) nanoparticles with a narrow sizedistribution were successfully synthesized by microwaveassistedusing urea as precipitant without surfactant ortemplate. The Sm2O3 particles were characterized using X-raydiffraction analysis, field-emission scanning electronmicroscopy, field-emission transmission electron microscopyand ultraviolet-visible-near-infrared spectrophotometer. Theresults showed that the samples prepared with differentconcentration of urea had different particle sizes. When theconcentration of urea was 1.2 mol/L, the sample had thesmallest particle size. A possible mechanism for the formationof the nanoparticles was proposed. Optical properties ofSm2O3 nanoparticles showed that the nanoparticles had astrong absorption property in the deep ultraviolet regionbetween 200 nm and 270 nm.
Involvement of Orai1 in tunicamycin-induced endothelial dysfunction
Yang, Hui,Xue, Yumei,Kuang, Sujuan,Zhang, Mengzhen,Chen, Jinghui,Liu, Lin,Shan, Zhixin,Lin, Qiuxiong,Li, Xiaohong,Yang, Min,Zhou, Hui,Rao, Fang,Deng, Chunyu The Korean Society of Pharmacology 2019 The Korean Journal of Physiology & Pharmacology Vol.23 No.2
Endoplasmic reticulum (ER) stress is mediated by disturbance of $Ca^{2+}$ homeostasis. The store-operated calcium (SOC) channel is the primary $Ca^{2+}$ channel in non-excitable cells, but its participation in agent-induced ER stress is not clear. In this study, the effects of tunicamycin on $Ca^{2+}$ influx in human umbilical vein endothelial cells (HUVECs) were observed with the fluorescent probe Fluo-4 AM. The effect of tunicamycin on the expression of the unfolded protein response (UPR)-related proteins BiP and CHOP was assayed by western blotting with or without inhibition of Orai1. Tunicamycin induced endothelial dysfunction by activating ER stress. Orai1 expression and the influx of extracellular $Ca^{2+}$ in HUVECs were both upregulated during ER stress. The SOC channel inhibitor SKF96365 reversed tunicamycin-induced endothelial cell dysfunction by inhibiting ER stress. Regulation of tunicamycin-induced ER stress by Orai1 indicates that modification of Orai1 activity may have therapeutic value for conditions with ER stress-induced endothelial dysfunction.
Involvement of Orai1 in tunicamycin-induced endothelial dysfunction
Hui Yang,Yumei Xue,Sujuan Kuang,Mengzhen Zhang,Jinghui Chen,Lin Liu,Zhixin Shan,Qiuxiong Lin,Xiaohong Li,Min Yang,Hui Zhou,Fang Rao,Chunyu Deng 대한약리학회 2019 The Korean Journal of Physiology & Pharmacology Vol.23 No.2
Endoplasmic reticulum (ER) stress is mediated by disturbance of Ca2+ homeostasis. The store-operated calcium (SOC) channel is the primary Ca2+ channel in non-excitable cells, but its participation in agent-induced ER stress is not clear. In this study, the effects of tunicamycin on Ca2+ influx in human umbilical vein endothelial cells (HUVECs) were observed with the fluorescent probe Fluo-4 AM. The effect of tunicamycin on the expression of the unfolded protein response (UPR)-related proteins BiP and CHOP was assayed by western blotting with or without inhibition of Orai1. Tunicamycin induced endothelial dysfunction by activating ER stress. Orai1 expression and the influx of extracellular Ca2+ in HUVECs were both upregulated during ER stress. The SOC channel inhibitor SKF96365 reversed tunicamycin-induced endothelial cell dysfunction by inhibiting ER stress. Regulation of tunicamycin-induced ER stress by Orai1 indicates that modification of Orai1 activity may have therapeutic value for conditions with ER stress-induced endothelial dysfunction.
( Zhen-quan Yang ),( Yu Xue ),( Sheng-qi Rao ),( Mi Zhang ),( Lu Gao ),( Yong-qi Yin ),( Da-wei Chen ),( Xiao-hui Zhou ),( Xin-an Jiao ) 한국미생물생명공학회(구 한국산업미생물학회) 2017 Journal of microbiology and biotechnology Vol.27 No.11
Piliated Lactobacillus rhamnosus (pLR) strains possess higher adherent capacity than non-piliated strains. The objective of this study was to isolate and characterize probiotic pLR strains in human fecal samples. To this end, mouse polyclonal antiserum (anti-SpaA) against the recombinant pilus protein (SpaA) of L. rhamnosus strain GG (LGG) was prepared and tested for its reactivity and specificity. With the anti-SpaA, a method combining the de Man, Rogosa, and Sharpe (MRS) agar plating separation and colony immunoblotting (CIB) was developed to isolate pLR from 124 human fecal samples. The genetic and phenotypic characteristics of the resultant pLR isolates were compared by randomly amplified polymorphic DNA (RAPD) fingerprinting, and examination of adhesion to Caco-2 cells, hydrophobicity, autoaggregation, and in vitro gastrointestinal tolerance. Anti-SpaA specifically reacted with three pLR strains of 25 test strains, as assessed by western blotting, immunofluorescence flow cytometry, and immunoelectron microscopy (IEM) assays. The optimized MRS agar separation plus anti- SpaA-based CIB procedure could quantitatively detect 2.5 × 10<sup>3</sup> CFU/ml of pLR colonies spiked in 10<sup>6</sup> CFU/ml of background bacteria. Eight pLR strains were identified in 124 human fecal samples, and were confirmed by 16S RNA gene sequencing and IEM identification. RAPD fingerprinting of the pLR strains revealed seven different patterns, of which only two isolates from infants showed the same RAPD profiles with LGG. Strain PLR06 was obtained with high adhesion and autoaggregation activities, hydrophobicity, and gastrointestinal tolerance. Anti-SpaA-based CIB is a rapid and inexpensive method for the preliminary screening of novel adherent L. rhamnosus strains for commercial purposes.