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RAPID DETERMINATION OF PROTEIN IN MILLET BY FOURIER TRANSFORM NEAR-INFRARED(FTNIR)DIFFUSE REFLECTANCE SPECTROSCOPY
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作者 Le Ming SHI Zhi Hong XU Zhong Xiao PAN Zhi Liang LI Laboratory of Computer Chemistry,Institute of Chemical Metallurgy,Chinese Academy of Sciences,Beijing 100080 Yan Lu YAN Mao JIN Central Laboratory,Beijing Agricultural University,Beijing 100094 《Chinese Chemical Letters》 SCIE CAS CSCD 1990年第3期247-250,共4页
In this paper,the Fourier transform near-infrared(FTNIR)diffuse reflectance spectroscopy is applied for the rapid determination of protein in millet.The partial least-squares(PLS)regression is successfully used as an ... In this paper,the Fourier transform near-infrared(FTNIR)diffuse reflectance spectroscopy is applied for the rapid determination of protein in millet.The partial least-squares(PLS)regression is successfully used as an effective multivariate calibration technique.The calibration set is composed of 20 standard millet samples that the protein contents were determined by the traditional Kjeldahl method.The optimal model dimension is found to be 5 by cross-validation.22 millet samples were determined by the proposed FTNIR-PLS method.The correlation coefficient between the concentration values obtained by the FTNIR-PLS method and the traditional Kjeldahl method is 0.9805.The standard error of prediction(SEP)is 0.28% and the mean recovery is 100.2%.The proposed method has been successfully applied for the routine analysis of protein in about 10,000 grain samples. 展开更多
关键词 PLS NIR FTNIR)DIFFUSE REFLECTANCE SPECTROSCOPY RAPID determination OF protein IN MILLET BY FOURIER TRANSFORM NEAR-INFRARED
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Determination of Isoflavone from Soybean Lines Cultivated in Jilin Province and Correlation Analysis between Isoflavone Content and Soybean Quality 被引量:29
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作者 宋向东 张之鑫 +1 位作者 王巍巍 富健 《Agricultural Science & Technology》 CAS 2010年第1期48-50,共3页
[Objective]The aim of this study was to set up a high performance liquid chromatography for rapid determination of isoflavones from soybean and analyze the correlation between isofalvone content and protein or fat con... [Objective]The aim of this study was to set up a high performance liquid chromatography for rapid determination of isoflavones from soybean and analyze the correlation between isofalvone content and protein or fat content. [Method]The isoflavones were firstly extracted by 80% methanol and then hydrolyzed at 100 ℃. The chromatographic separation adopted a reversed-phase C18 analytical column with binary high-pressure gradient elution,while its analysis time was 25 min and column temperature was 40 ℃. The diode array detector was used for monitoring with wavelength of 260 nm. The correlation between isofalvone content and protein or fat content was analyzed by data processing system Origin 6.0. [Result]The high performance liquid chromatograph for determination of isoflavones from soybean was verified to be accurate and reliable by methodology. The isoflavones of 85 soybean lines cultivated in Jilin Province were determined,and the results primarily showed the characters and ranges of isoflavones from soybean lines cultivated in Jilin Province,while the isoflavone content of soybeans ranged from 2.29 to 4.89 mg/g,and the average content was 3.36 mg/g. The isoflavone content of 5 soybean lines exceeded 4 mg/g,while there was a remarkably negative correlation between isoflavone content and protein content,and there was no significant positive correlation between isoflavone content and fat content. [Conclusion]The isoflavone content of soybean lines cultivated in Jilin Province is higher,so it is feasible for breeding the soybean lines with high isoflavone content and fat contetnt. 展开更多
关键词 Cultivated soybean Isoflavone content determination protein content Fat content
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Male sex determination: insights into molecular mechanisms 被引量:8
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作者 Kathryn McClelland Josephine Bowles Peter Koopman 《Asian Journal of Andrology》 SCIE CAS CSCD 2012年第1期164-171,180,共9页
Disorders of sex development often arise from anomalies in the molecular or cellular networks that guide the differentiation of the embryonic gonad into either a testis or an ovary, two functionally distinct organs. T... Disorders of sex development often arise from anomalies in the molecular or cellular networks that guide the differentiation of the embryonic gonad into either a testis or an ovary, two functionally distinct organs. The activation of the Y-linked gene Sry (sex- determining region Y) and its downstream target Sox9 (Sry box-containing gene 9) triggers testis differentiation by stimulating the differentiation of Sertoli cells, which then direct testis morphogenesis. Once engaged, a genetic pathway promotes the testis development while actively suppressing genes involved in ovarian development. This review focuses on the events of testis determination and the struggle to maintain male fate in the face of antagonistic pressure from the underlying female programme. 展开更多
关键词 gonadal KNOCKOUT MICE sex determination sex-determining region Y protein sex disorders sex reversal sexual development TESTIS
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Identification of Three Interactions to Determine the Conformation Change and to Maintain the Function of Kir2.1 Channel Protein
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作者 李军委 肖少英 +4 位作者 谢潇潇 于慧 张海林 展永 安海龙 《Chinese Physics Letters》 SCIE CAS CSCD 2015年第2期163-165,共3页
We find that a conserved mutation residue Glu to residue Asp (E303D), which both have the same polar and charged properties, makes Kit2.1 protein lose its function. To understand the mechanism, we identify three int... We find that a conserved mutation residue Glu to residue Asp (E303D), which both have the same polar and charged properties, makes Kit2.1 protein lose its function. To understand the mechanism, we identify three interactions which control the conformation change and maintain the function of the Kit2.1 protein by combining homology modeling and molecular dynamics with targeted molecular dynamics. We find that the E303D mutation weakens these interactions and results in the loss of the related function. Our data indicate that not only the amino residues but also the interactions determine the function of proteins. 展开更多
关键词 In Identification of Three Interactions to determine the Conformation Change and to Maintain the Function of Kir2.1 Channel protein
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Development of a competitive array for discriminative determination of amphenicols in egg based on ribosomal protein L16
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作者 才艺 马宁 +1 位作者 吴宁鹏 王建平 《Food Quality and Safety》 SCIE CAS CSCD 2024年第1期105-114,共10页
Objective:Amphenicols(chloramphenicol,thiamphenicol and forfenicol)can cause aplastic anaemia and other severe side effects to consumers;therefore,it is necessary to inspect their residues in foods of animal origin.Ho... Objective:Amphenicols(chloramphenicol,thiamphenicol and forfenicol)can cause aplastic anaemia and other severe side effects to consumers;therefore,it is necessary to inspect their residues in foods of animal origin.However,there has been no report on the use of amphenicols receptor for the determination of their residues,and none of the previously reported immunoassays for amphenicols can differentiate the specifc species.Materials and Methods:In this study,the ribosomal protein L16 of Escherichia coli was frst expressed,and its intermolecular interaction mechanisms with the three amphenicols was studied using the molecular docking technique.The protein was then combined with three enzymelabelled conjugates to develop a direct competitive array on microplate for determination of the three drugs in egg.Results:Due to the use of principal component analysis to analyse the data,this method could discriminate the three drugs in the range 0.1–10 ng/mL,and the limits of detection for the three drugs were in the range of 0.0002–0.0009 ng/mL.The analysis results for the unknown egg samples were consistent with a liquid chromatography–tandem mass spectrometry method,and the method performances were superior to the previous immunoassays for amphenicols.Conclusion:This is the frst paper reporting the use of ribosomal protein L16 to develop a competitive array for discriminative determination of amphenicols in food samples. 展开更多
关键词 Amphenicols ribosomal protein L16 recognition mechanism competitive array discriminative determination egg.
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C-reactive protein as a predictor for cardiac events in Chinese elderly patients with coronary heart disease 被引量:1
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作者 Guangyong HUANG Caiyi LU Xingli WU Yuxiao ZHANG 《Journal of Geriatric Cardiology》 SCIE CAS CSCD 2006年第2期78-81,共4页
Background and objective To assess the predictive value of C-reactive protein(CRP) for major adverse cardiac events and the association between CRP level and the coronary lesion morphology and extent in patients with ... Background and objective To assess the predictive value of C-reactive protein(CRP) for major adverse cardiac events and the association between CRP level and the coronary lesion morphology and extent in patients with coronary heart disease (CHD).Methods CRP was measured on admission in 177 consecutive elderly (age≥60 years) patients with CHD who underwent coronary angiography. Patients were divided into high CRP group (CRP≥3mg/L) and normal CRP group (CRP <3mg/L). The association between CRP levels and the coronary lesion features, including severity of stenosis (mild, moderate, severe), extent of lesion (diffused or nondiffused), eccentricity of the plaque (eccentric or non-eccentric) were analyzed. Patients were followed up for a mean of 8 months for the occurrences of major adverse cardiac events (MACE). Results Compared with patients in normal CRP group, patients in high CRP group were more frequently to have unstable angina, multi-vessel, diffuse, eccentric lesions, positive remodeling, and non-smooth plaques (P<0.01). Kaplan-Meier analysis showed patients in high CRP group had a significantly lower MACE-free survival rate than patients in normal CRP group (Log-rank = 12.0, P<0.01); Cox regression analysis indicated CRP level as an independent predictor for the occurrence of MACE (OR=3.16, P<0.05) Conclusions High CRP level is associated with more extend, severe and eccentric coronary lesions and is an independent predictor for MACE in elderly patients with CHD. 展开更多
关键词 c-reaction protein CORONARY ARTERY disease ANGIOGRAPHY major ADVERSE CARDIAC events
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Methodological approach to the isolation of functionally active proteins from the tissues of marine hydrobionts: an example of Adamussium colbecki
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作者 Nataliia Raksha Dmytro Gladun +1 位作者 Oleksii Savchuk Lydmila Ostapchenko 《Advances in Polar Science》 2015年第4期299-304,共6页
Enzymes from cold-adapted organisms have significant application potential. Because of their unique properties they have been found to be useful in various industries. Despite indisputable practical interest, cold act... Enzymes from cold-adapted organisms have significant application potential. Because of their unique properties they have been found to be useful in various industries. Despite indisputable practical interest, cold active enzymes also represent a valuable model for fundamental research into protein folding and catalysis. Many investigators have focused their attention on marine hydrobionts, which are growing in importance as a promising source of enzymes. The nature of the source not only determines the availability and the cost of biomolecules of interest but also determines the choice of method for their extraction. A simple and convenient methodological approach of two-stage extraction of proteins has been tested on the Antarctic marine hydrobiont--Adamussium colbecki. This method extracts enough effective protein directly from primary raw materials, as well as when using leftover crude precipitates. The electrophoretic pattern of proteins showed the presence of molecules in a wide range of molecular weights in the samples of A. colbecki after the first and the second stage of extraction. The general proteolytic activity in the first and the second extracts were examined using a zymogram technique. Our experiments revealed that the second extract of A. colbecki contained thermo stable protease exhibiting a molecular weight of 95 kDa in a gelatin zymogram. Further biochemical assays, using different substrates, were conducted to partially identify the types of hydrolases present in the first and the second extracts. Our results revealed the presence of enzymes with collagenolytic and some amylolytic activities preserved in the second extracts. But no esterase or amidase trypsin-like activities were found in the second extract, in contrast to the first extract where this type of activity was significant. 展开更多
关键词 Antarctic marine hydrobiont protein extraction enzyme activity determination
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先天性巨结肠患儿术后肠道组织中CAD、SOX2的表达水平及其临床意义
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作者 张宁 岳铭 袁宇航 《海南医学》 CAS 2024年第7期939-943,共5页
目的探讨先天性巨结肠(HD)患儿术后肠道组织蛋白酶D(CAD)、性别决定区Y框蛋白2(SOX2)的表达水平及其临床意义。方法选取2015年5月至2019年3月郑州大学第一附属医院收治的56例HD患儿结肠组织(HD组)和23例因肠道梗阻或穿孔实施造瘘手术获... 目的探讨先天性巨结肠(HD)患儿术后肠道组织蛋白酶D(CAD)、性别决定区Y框蛋白2(SOX2)的表达水平及其临床意义。方法选取2015年5月至2019年3月郑州大学第一附属医院收治的56例HD患儿结肠组织(HD组)和23例因肠道梗阻或穿孔实施造瘘手术获取的结肠组织标本(对照组)。采用免疫组化、Western-blot技术检测结肠组织中CAD、SOX2的表达水平,并采用Pearson线性相关分析法分析CAD、SOX2表达与病变肠段肌间神经丛直径、神经节细胞数的关系。结果HD患儿的狭窄段组织中CAD蛋白、SOX2蛋白阳性表达率分别为7.14%、12.50%,移行段肠组织中CAD蛋白、SOX2蛋白阳性表达率分别为32.14%、35.71%,明显低于对照组的78.26%、82.61%,而狭窄段组织中CAD蛋白、SOX2蛋白阳性表达率明显低于移行段,差异均有统计学意义(P<0.05);HD患儿的狭窄段肠组织中肌间神经丛直径、神经节细胞数目分别为(30.66±5.14)μm、(0.83±0.24)个/视野,移行段肠组织中肌间神经丛直径、神经节细胞数目分别为(31.20±5.83)μm、(1.94±0.56)个/视野,明显短(少)于对照组的(54.29±8.50)μm、(5.40±1.84)个/视野,狭窄段肠组织中肌间神经丛直径、神经节细胞数目明显短(少)于移行段,差异均有统计学意义(P<0.05);Pearson相关分析结果显示,HD患儿狭窄段、移行段肠组织中肌间神经丛直径、神经节细胞数目与CAD蛋白、SOX2蛋白表达强度均呈显著正相关(P<0.05)。结论HD患儿病变结肠组织中CAD蛋白、SOX2蛋白的表达强度下调,可能与肌间神经丛直径、神经节细胞数目的减少有关。 展开更多
关键词 先天性巨结肠 组织蛋白酶D 性别决定区Y框蛋白2 相关性
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非小细胞肺癌组织中miR-363-3p、SOX4 mRNA表达及对上皮间质转化进程的影响
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作者 吴会丽 柴静 +2 位作者 李应龙 封敏 霍怡杉 《山东医药》 CAS 2024年第22期1-4,共4页
目的探讨非小细胞肺癌组织中微小RNA-363-3p(miR-363-3p)、性别决定区Y框蛋白4(SOX4)表达及对上皮间质转化(EMT)进程的影响。方法收集行手术切除的84例非小细胞肺癌患者的癌及其癌旁组织。采用实时荧光定量聚合酶链反应检测癌及癌旁组织... 目的探讨非小细胞肺癌组织中微小RNA-363-3p(miR-363-3p)、性别决定区Y框蛋白4(SOX4)表达及对上皮间质转化(EMT)进程的影响。方法收集行手术切除的84例非小细胞肺癌患者的癌及其癌旁组织。采用实时荧光定量聚合酶链反应检测癌及癌旁组织miR-363-3p、SOX4 mRNA表达,免疫组化SP法检测癌及癌旁组织中E-cadherin、Vimentin表达。比较不同病理特征患者癌组织中miR-363-3p、SOX4 mRNA表达,采用Spearman秩相关分析癌组织miR-363-3p、SOX4 mRNA表达与E-cadherin、Vimentin相关性。使用相对超危险度比(RERI)、归因比(AP)、交互作用指数(SI)分析miR-363-3p、SOX4参与EMT进程的交互作用。结果癌组织中miR-363-3p表达低于癌旁组织,SOX4 mRNA表达高于癌旁组织(P均<0.05);癌组织中miR-363-3p、SOX4 mRNA表达与性别、年龄、吸烟史、肿瘤最大径无关(P均>0.05),与分化程度、TNM分期有关(P均<0.05);癌组织E-cadherin阳性表达率低于癌旁组织,Vimentin阳性表达率高于癌旁组织(P均<0.05);癌组织miR-363-3p与E-cadherin表达呈正相关(r=0.491,P<0.05),与Vimentin表达呈负相关(r=-0.506,P<0.05);癌组织SOX4 mRNA与E-cadherin表达呈负相关(r=-0.527,P<0.05),与Vimentin表达呈正相关(r=0.463,P<0.05)。癌组织miR-363-3p、SOX4对EMT进程存在负向交互作用(RERI=29.639,AP=70.91,SI=3.656)。结论非小细胞肺癌组织中miR-363-3p、SOX4异常表达与EMT有关,且二者对EMT进程存在负向交互作用。 展开更多
关键词 非小细胞肺癌 微小RNA-363-3p 性别决定区Y框蛋白4 上皮间质转化
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血清金属蛋白酶组织抑制剂3和性别决定区Y框蛋白2在2型糖尿病肾损伤早期诊断中的临床应用
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作者 张洪利 王海成 +2 位作者 李华 未瑞超 曾玲 《临床肾脏病杂志》 2024年第7期529-535,共7页
目的探究血清金属蛋白酶组织抑制剂3(tissue inhibitors of metalloproteinases 3,TIMP3)和性别决定区Y框蛋白2(transcription factor determining region Y box protein 2,SOX2)对2型糖尿病(type 2 diabetes mellitus,T2DM)肾损伤的早... 目的探究血清金属蛋白酶组织抑制剂3(tissue inhibitors of metalloproteinases 3,TIMP3)和性别决定区Y框蛋白2(transcription factor determining region Y box protein 2,SOX2)对2型糖尿病(type 2 diabetes mellitus,T2DM)肾损伤的早期诊断。方法选取2022年4月至2023年4月在华北石油管理局总医院就诊的102例T2DM患者为研究对象,根据24 h尿蛋白排泄率(uri-nary albumin excretion rate,UAER)将T2DM患者分为肾损伤组(n=40)和无肾损伤组(n=62),另选取同期在华北石油管理局总医院行体检的健康者50名为对照组。酶联免疫吸附法测定所有受试者血清TIMP3、SOX2水平;比较3组受试者一般资料、糖化血红蛋白(hemoglobin A1c,HbA1c)、UAER、血肌酐(serum creatinine,Scr)、估算肾小球滤过率(estimated glomerular filtration rate,eGFR)、血清TIMP3、SOX2水平;Pearson相关性分析血清TIMP3与SOX2及两者与HbA1c、UAER、Scr、eGFR之间的关系;受试者工作特征曲线(receiver operating characteristic curve,ROC)分析血清TIMP3、SOX2对T2DM患者肾损伤的诊断价值。结果T2DM患者血清TIMP3[(0.68±0.17)μg/L比(1.35±0.35)μg/L]及eGFR[(105.99±20.56)mL·min^(-1)·(1.73 m^(2))比(133.15±26.18)mL·min^(-1)·(1.73 m^(2))^(-1)]显著低于对照组(P<0.05),且肾损伤患者血清TIMP3[(0.47±0.11)μg/L比(0.82±0.21)^(-1)μg/L]及eGFR[(74.69±10.22)mL·min^(-1)·(1.73 m^(2))比(126.18±27.23)mL·min^(-1)·(1.73 m^(2))^(-1)]显著低于无肾损伤患者(P<0.05);血清SOX2[(8.91±1.82)kU/L比(5.15±1.31)kU/L]及HbA1c[(8.80±1.55)%比(5.52±0.83)%]、UAER[(70.13±18.06)mg/24 h比(13.22±3.61)mg/24 h]、Scr[(82.14±15.23)µmol/L比(53.19±5.62)µmol/L]显著高于对照组(P<0.05),且肾损伤患者血清SOX2[(10.81±2.13)kU/L比(5.15±1.31)kU/L]及UAER[(156.83±40.29)mg/24 h比(13.22±3.61)mg/24 h]、Scr[(113.77±13.58)µmol/L比(53.19±5.62)µmol/L]显著高于无肾损伤患者(P<0.05)。Pearson相关性分析结果显示,TIMP3与UAER、Scr、HbA1c呈显著负相关(P<0.05),与eGFR呈显著正相关(P<0.05);SOX2与UAER、Scr、HbA1c呈显著正相关(P<0.05),与eGFR呈显著负相关(P<0.05);血清TIMP3与SOX2呈显著负相关(r=-0.590,P<0.05)。ROC结果显示,血清TIMP3联合SOX2诊断T2DM患者肾损伤的敏感度和特异度分别为95.0%、85.3%,显著高于TIMP3、SOX2单独测定。结论T2DM肾损伤患者血清TIMP3水平显著降低,SOX2水平显著升高,且两者与T2DM患者肾损伤密切相关,可用于T2DM患者肾损伤早期诊断。 展开更多
关键词 金属蛋白酶组织抑制剂3 性别决定区框蛋白2 2型糖尿病 肾损伤 早期诊断
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SOX7靶向ERK1/2/PD-L1通路抑制结直肠癌血管生成
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作者 武雪亮 王立坤 +3 位作者 马洪庆 路永刚 李少东 惠志龙 《解剖学研究》 CAS 2024年第3期208-215,共8页
目的探讨性别决定区Y框蛋白7(SOX7)对结直肠癌血管生成的影响及潜在作用机制。方法应用免疫荧光检测结直肠癌患者组织样本中SOX7表达水平,之后通过裸鼠、转染SOX7 mimic的人结直肠癌细胞系SW480细胞和人脐静脉内皮细胞(HUVEC)共培养进... 目的探讨性别决定区Y框蛋白7(SOX7)对结直肠癌血管生成的影响及潜在作用机制。方法应用免疫荧光检测结直肠癌患者组织样本中SOX7表达水平,之后通过裸鼠、转染SOX7 mimic的人结直肠癌细胞系SW480细胞和人脐静脉内皮细胞(HUVEC)共培养进一步研究。用Western-blot验证SOX7与ERK1/2/PD-L1对结直肠癌细胞的相关蛋白表达的影响。用CCK8检测SOX7与ERK1/2/PD-L1对HUVEC增殖的影响。通过体外内皮细胞成管实验测定SOX7与ERK1/2/PD-L1对肿瘤血管生成的影响。结果SOX7在人结直肠癌组织中表达被抑制(P<0.01),同时SOX7的过表达抑制了小鼠体内肿瘤生长(P<0.01)。SW480细胞中SOX7的过表达抑制了ERK1/2、c-Jun的表达,并在ERK1/2的激动剂Senkyunolide I的作用下上调了SW480细胞的ERK1/2、c-Jun蛋白表达(P<0.01),逆转了SOX7对SW480细胞中ERK1/2、c-Jun蛋白表达的影响(P<0.01)。HUVEC中SOX7抑制了PD-L1、V-EGFR2、p-PI3K、HIF-1α的蛋白表达,Senkyunolide I上调了HUVEC的PD-L1、V-EGFR2、p-PI3K、HIF-1α的蛋白表达,并逆转了SOX7对HUVEC中上述相关蛋白表达的影响(P<0.01)。PD-1/PD-L1 Inhibitor 3抑制了PD-L1、V-EGFR2、p-PI3K、HIF-1α的蛋白表达,SOX7过表达在PD-1/PD-L1 Inhibitor 3的影响下并没有表现出抑制作用。CCK8实验结果显示SOX7过表达显著抑制了HUVEC的增殖能力,Senkyunolide I作用下的两组HUVEC增殖能力较SOX7 NC组与SOX7 mimic组明显上升,PD-1/PD-L1 Inhibitor 3作用下的两组HUVEC增殖能力较SOX7 NC组与SOX7 mimic组明显下降,以上均有明显统计学差异(P<0.01)。成管实验结果显示SOX7过表达抑制了HUVEC的血管生成,Senkyunolide I强烈加速了血管生成,而PD-1/PD-L1 Inhibitor 3血管生成则被显著抑制,以上均有明显统计学差异(P<0.01)。结论SOX7通过ERK1/2/PD-L1通路抑制结直肠肿瘤的增殖和血管生成,SOX7可能是晚期CRC患者临床治疗中潜在的抗血管生成靶点。 展开更多
关键词 结直肠癌 性别决定区Y框蛋白7(SOX7) 细胞外调节蛋白激酶(ERK1/2) 细胞程序性死亡-配体1(PD-L1) 增殖 血管生成 人结直肠癌细胞系SW480细胞
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斑蝥酸钠注射液中蛋白质的含量测定
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作者 田甜 祝晶 +2 位作者 曹桂红 徐波 王璐 《山东化工》 CAS 2024年第17期193-195,共3页
目的:建立2,2′-联喹啉-4,4′-二羧酸(BCA)测定斑蝥酸钠注射液中残留蛋白质含量的方法。方法:依据蛋白质分子在碱性溶液中将Cu^(2+)还原为Cu^(+),2,2′-联喹啉-4,4′-二羧酸(BCA)与Cu^(+)结合形成紫色复合物,在一定范围内其颜色深浅与... 目的:建立2,2′-联喹啉-4,4′-二羧酸(BCA)测定斑蝥酸钠注射液中残留蛋白质含量的方法。方法:依据蛋白质分子在碱性溶液中将Cu^(2+)还原为Cu^(+),2,2′-联喹啉-4,4′-二羧酸(BCA)与Cu^(+)结合形成紫色复合物,在一定范围内其颜色深浅与蛋白质浓度呈正比,以蛋白质对照品溶液作标准曲线,采用紫外-分光光度法测定供试品中蛋白质含量。结果:蛋白质在20~100μg范围内,线性关系良好(R=0.9979),精密度RSD为1.6%,稳定性RSD为3.2%,重现性RSD为3.2%,平均回收率为93%,RSD为1.3%(n=9)。结论:此方法专属性强、精密度稳定性良好、准确度较高,可用作斑蝥酸钠中蛋白质的含量测定方法,确保用药安全及关注厂家的工艺是否合理并建立斑蝥酸钠中蛋白质残留的检测标准,以便更科学地进行斑蝥酸钠的质量控制。 展开更多
关键词 斑蝥酸钠注射液 蛋白质 含量测定 BCA
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基于凯氏定氮法测定食物蛋白质含量要素探究 被引量:1
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作者 周俞宏 《工业微生物》 CAS 2024年第2期200-202,共3页
为进一步提高凯氏定氮法测定食物蛋白质含量的精准度,相关测定人员应全面、系统地掌握凯氏定氮测定法的所有流程,并了解其相关公式技巧等。为实现这一目标,文章结合相关经验和文献资料,在对凯氏定氮法测定食物蛋白质含量的原理、优缺点... 为进一步提高凯氏定氮法测定食物蛋白质含量的精准度,相关测定人员应全面、系统地掌握凯氏定氮测定法的所有流程,并了解其相关公式技巧等。为实现这一目标,文章结合相关经验和文献资料,在对凯氏定氮法测定食物蛋白质含量的原理、优缺点、步骤等分析的基础上,以鸡蛋食物蛋白质为例,对相关测定要素进行探讨,以供参考。 展开更多
关键词 凯氏定氮法 食物蛋白质 鸡蛋 含量测定
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SOX4和SOX12基因在多发性骨髓瘤中的表达及其与临床病理特征及预后的相关性 被引量:1
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作者 郜晓 朱凯 +2 位作者 许纯 潘迎英 宋丽丽 《检验医学与临床》 CAS 2024年第11期1640-1645,共6页
目的探讨性别决定区Y框蛋白4(SOX4)和性别决定区Y框蛋白12(SOX12)基因在多发性骨髓瘤患者血清中的表达,及其与临床病理特征及预后的相关性。方法选取2019年5月至2020年5月该院诊治的87例多发性骨髓瘤患者作为研究组,对患者进行3年随访,... 目的探讨性别决定区Y框蛋白4(SOX4)和性别决定区Y框蛋白12(SOX12)基因在多发性骨髓瘤患者血清中的表达,及其与临床病理特征及预后的相关性。方法选取2019年5月至2020年5月该院诊治的87例多发性骨髓瘤患者作为研究组,对患者进行3年随访,根据3年内的预后情况分为生存组和死亡组,另选取同期在该院体检的87例健康者作为对照组。采用Pearson相关分析SOX4基因表达水平与SOX12基因表达水平的相关性;采用受试者工作特征(ROC)曲线分析SOX4和SOX12基因对多发性骨髓瘤患者预后的预测效能;采用Kaplan-Meier生存曲线分析多发性骨髓瘤患者SOX4和SOX12基因表达与患者生存率的关系。结果研究组SOX4和SOX12基因表达水平均高于对照组,差异均有统计学意义(P<0.05);多发性骨髓瘤患者SOX4基因表达水平与SOX12基因表达水平呈正相关(r=0.689,P<0.05);不同ISS分期多发性骨髓瘤患者SOX4、SOX12基因表达情况比较,差异均有统计学意义(P<0.05)。不同SOX4、SOX12基因表达情况多发性骨髓瘤患者HbA1c、CRP、PLT、血清钙水平比较,差异均有统计学意义(P<0.05)。死亡组SOX4和SOX12基因表达水平均高于生存组,差异均有统计学意义(P<0.05);SOX4和SOX12基因单独检测评估多发性骨髓瘤患者预后的曲线下面积(AUC)分别为0.631、0.771,二者联合检测的AUC为0.839,AUC明显大于SOX4和SOX12基因各自单独检测的AUC(Z二者联合与SOX4=2.142、P=0.032,Z二者联合与SOX12=3.833、P<0.001);SOX4基因高表达患者3年生存率(63.64%)低于SOX4基因低表达患者(83.08%),差异有统计学意义(χ^(2)=4.544,P=0.033),且生存时间也少于SOX4基因低表达患者;SOX12基因高表达患者3年生存率(53.84%)低于SOX12基因低表达患者(82.43%),差异有统计学意义(χ^(2)=6.402,P=0.011),且生存时间也少于SOX12基因低表达患者。结论多发性骨髓瘤患者SOX4和SOX12基因表达水平与临床病理特征及预后关系密切,二者联合检测对多发性骨髓瘤患者的预后具有较高预测效能。 展开更多
关键词 多发性骨髓瘤 性别决定区Y框蛋白4 性别决定区Y框蛋白12 临床病理特征 预后
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Involvement of C2H2 zinc finger proteins in the regulation of epidermal cell fate determination in Arabidopsis 被引量:7
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作者 An Yan Minjie Wu +4 位作者 Yongqin Zhao Aidong Zhang Bohan Liu John Schiefelbein Yinbo Gan 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2014年第12期1112-1117,共6页
Cell fate determination is a basic developmental process during the growth of multicellular organisms.Trichomes and root hairs of Arabidopsis are both readily accessible structures originating from the epidermal cells... Cell fate determination is a basic developmental process during the growth of multicellular organisms.Trichomes and root hairs of Arabidopsis are both readily accessible structures originating from the epidermal cells of the aerial tissues and roots respectively, and they serve as excellent models for understanding the molecular mechanisms controlling cell fate determination and cell morphogenesis. The regulation of trichome and root hair formationis a complex program that consists of the integration of hormonal signals with a large number of transcriptional factors, including MYB and b HLH transcriptional factors.Studies during recent years have uncovered an important role of C2H2 type zinc finger proteins in the regulation of epidermal cell fate determination. Here in this minireview we briefly summarize the involvement of C2H2 zinc finger proteins in the control of trichome and root hair formation in Arabidopsis. 展开更多
关键词 C2H2 cell fate determination root hair trichome zinc finger protein
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补肾痹通方联合骨髓间充质干细胞对损伤软骨细胞的保护机制及SOX9、MMP-13表达的影响
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作者 易林 向文远 +4 位作者 张文豪 石正誉 热米拉·艾买提 邓迎杰 方锐 《陕西中医》 CAS 2024年第6期728-732,739,共6页
目的:探讨补肾痹通方(BSBT)联合骨髓间充质干细胞(BMSCs)对白介素(IL)-1β诱导的损伤软骨细胞的保护机制及性别决定区Y框蛋白9(SOX9)、基质金属蛋白酶13(MMP-13)表达的影响。方法:使用10 ng/ml的IL-1β建立损伤软骨细胞模型,实验分为对... 目的:探讨补肾痹通方(BSBT)联合骨髓间充质干细胞(BMSCs)对白介素(IL)-1β诱导的损伤软骨细胞的保护机制及性别决定区Y框蛋白9(SOX9)、基质金属蛋白酶13(MMP-13)表达的影响。方法:使用10 ng/ml的IL-1β建立损伤软骨细胞模型,实验分为对照组、模型组(IL-1β)、中药组(IL-1β+BSBT)、干细胞组(IL-1β+BMSCs)和联合组(IL-1β+BSBT+BMSCs);CCK-8法检测各组软骨细胞增殖情况;RT-qPCR法和Western blot法分别检测软骨细胞内SOX9、MMP-13、Ⅱ型胶原α1重组蛋白(COL2A1)、IL-10的基因和蛋白表达;ELISA检测各组细胞培养上清中肿瘤坏死因子-α(TNF-α)、IL-6、胰岛素样生长因子1(IGF-1)、碱性成纤维细胞生长因子(bFGF)的水平。结果:与模型组比较,各组软骨细胞活性显著增强(P<0.01),软骨细胞中的SOX9、COL2A1、IL-10的基因和蛋白水平显著升高(P<0.01),MMP-13的基因和蛋白水平明显降低(P<0.01),软骨细胞培养上清中TNF-α、IL-6的含量显著降低(P<0.01),IGF-1、bFGF的水平升高(P<0.01),其中联合组变化最明显(P<0.05)。结论:BSBT联合BMSCs可有效保护损伤软骨细胞,其机制可能是通过上调SOX9,下调MMP-13,抑制炎症,改善软骨细胞微环境,促进关节软骨的修复与再生。 展开更多
关键词 骨关节炎 补肾痹通方 骨髓间充质干细胞 软骨细胞 性别决定区Y框蛋白9 基质金属蛋白酶13
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circPVT1靶向调控miR-195-5p/SOX9轴影响结肠癌细胞增殖、凋亡及上皮间质转化
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作者 刘光世 李涛 +3 位作者 李鹏 马占军 张旺 袁传威 《现代肿瘤医学》 CAS 2024年第12期2189-2195,共7页
目的:探究环状RNA浆细胞瘤变体易位1(circPVT1)靶向调控微小RNA-195-5p(miR-195-5p)/性别决定区Y框蛋白9(SOX9)轴对结肠癌细胞增殖、凋亡及上皮间质转化(EMT)的影响。方法:体外培养人正常结肠上皮细胞NCM-460、人结肠癌细胞系(SW480、HC... 目的:探究环状RNA浆细胞瘤变体易位1(circPVT1)靶向调控微小RNA-195-5p(miR-195-5p)/性别决定区Y框蛋白9(SOX9)轴对结肠癌细胞增殖、凋亡及上皮间质转化(EMT)的影响。方法:体外培养人正常结肠上皮细胞NCM-460、人结肠癌细胞系(SW480、HCT116、HCT29、LOVO、SW620)至对数期,将SW480细胞分为对照组(正常培养SW480细胞不进行转染)、空载质粒组(转染空载质粒)、circPVT1沉默组[转染circPVT1小干扰RNA(siRNA)质粒]、miR-195-5p过表达组[转染miR-195-5p模拟物(mimics)质粒]、SOX9沉默组(转染SOX9 siRNA质粒)、circPVT1沉默+miR-195-5p低表达组(转染circPVT1 siRNA和miR-195-5p siRNA质粒)。各组转染相应质粒后培养48 h。荧光定量PCR法检测NCM-460细胞、人结肠癌细胞系(SW480、HCT116、HCT29、LOVO、SW620)和各组SW480细胞circPVT1、miR-195-5p、SOX9 mRNA的表达;噻唑蓝和流式细胞仪分别检测各组SW480细胞增殖和凋亡;蛋白印迹法检测各组SW480细胞SOX9、凋亡和EMT相关蛋白表达;双荧光素酶报告基因实验检测circPVT1与miR-195-5p、miR-195-5p与SOX9的靶向关系。结果:与NCM-460细胞比较,SW480细胞、HCT116细胞、HCT29细胞、LOVO细胞、SW620细胞中circPVT1、SOX9 mRNA表达显著升高,miR-195-5p表达显著降低(P<0.05);其中,SW480细胞中circPVT1、SOX9 mRNA表达最高,miR-195-5p表达最低;故选择SW480细胞进行后续实验。与对照组和空载质粒组比较,circPVT1沉默组circPVT1、SOX9 mRNA及蛋白表达显著降低,miR-195-5p表达显著升高(P<0.05);miR-195-5p过表达组miR-195-5p表达显著升高,SOX9 mRNA及蛋白表达显著降低(P<0.05);SOX9沉默组SOX9 mRNA及蛋白表达显著降低(P<0.05)。与对照组和空载质粒组比较,circPVT1沉默组、miR-195-5p过表达组、SOX9沉默组细胞增殖率、Bcl-2、Vimentin蛋白表达显著降低,凋亡率、Bax、E-cadherin蛋白表达显著升高(P<0.05)。与circPVT1沉默组比较,circPVT1沉默+miR-195-5p低表达组miR-195-5p、凋亡率、Bax、E-cadherin蛋白表达显著降低,SOX9 mRNA及蛋白、细胞增殖率、Bcl-2、Vimentin蛋白表达显著升高(P<0.05)。circPVT1与miR-195-5p、miR-195-5p与SOX9存在靶向调控关系。结论:沉默circPVT1可以靶向上调miR-195-5p表达,抑制SOX9表达,进而抑制SW480细胞增殖和EMT进程,促进其凋亡。 展开更多
关键词 环状RNA浆细胞瘤变体易位1 微小RNA-195-5p 性别决定区Y框蛋白9 结肠癌 上皮间质转化
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SOX9通过转化生长因子β信号通路调节角膜内皮损伤后内皮-间质转化过程
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作者 孙图南 李晓琦 +2 位作者 李宗源 黄一飞 王丽强 《联勤军事医学》 CAS 2024年第1期6-10,共5页
目的探究性别决定区Y框蛋白9(sex-determining region Y-box protein 9,SOX9)是否会调控角膜内皮细胞损伤后的角膜上皮-间质转化(endothelial-to-mesenchymal transition,EndMT)过程及具体机制。方法转染小干扰RNA(small interfering RN... 目的探究性别决定区Y框蛋白9(sex-determining region Y-box protein 9,SOX9)是否会调控角膜内皮细胞损伤后的角膜上皮-间质转化(endothelial-to-mesenchymal transition,EndMT)过程及具体机制。方法转染小干扰RNA(small interfering RNA,siRNA)敲低人角膜内皮细胞B4G12中SOX9的表达,使用甲萘醌构建体外B4G12细胞损伤模型,设4个分组:si-NC组(转染siRNA-阴性对照)、si-SOX9组(转染siRNA-SOX9)、si-NC+甲萘醌组(转染siRNA-阴性对照后添加外源性甲萘醌做损伤处理)、si-SOX9+甲萘醌组(转染siRNA-SOX9后添加外源性甲萘醌做损伤处理)。通过实时荧光逆转录聚合酶链反应(real-time reverse transcription polymerase chain reaction,RT-PCR)和Western blot检测各组细胞中EndMT关键因子Snail家族转录抑制因子2(snail family transcriptional repressor 2,SNAIL2)及相关信号通路关键因子表达变化,阐明SOX9调控EndMT过程的功能和机制。结果转染siRNA-SOX9敲低细胞SOX9表达后,给予甲萘醌细胞损伤处理,观察到细胞中SNAIL2的表达会随SOX9的敲低而降低,同时观察到转化生长因子β(transforming growth factor beta,TGF-β)信号通路中SNAIL2的上游关键因子Smad2/Smad3的表达也随着SOX9的敲低而降低。结论SOX9通过TGF-β信号通路调控角膜内皮损伤后EndMT过程。 展开更多
关键词 角膜内皮细胞 性别决定区Y框蛋白9 Snail家族转录抑制因子2 上皮-间质转化 转化生长因子β信号通路
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食药用菌蛋白质研究现状及应用
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作者 陈亭菊 刘远超 +4 位作者 蔡曼君 郭慧阳 陈少丹 吴清平 胡惠萍 《食用菌学报》 CSCD 北大核心 2024年第2期113-126,共14页
食药用菌是优质的蛋白质来源,介绍食药用菌蛋白质的提取、含量测定方法,探讨食药用菌蛋白质的氨基酸组成、营养评价及其来源、种类、功能,总结食药用菌蛋白质在医药、食品及生物防治方面的应用,并对食药用菌蛋白质的发展前景进行展望。
关键词 食药用菌 蛋白质 凯氏定氮法 抗肿瘤 蛋白质组学
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Matrix Assisted Laser Desorption lonization Mass Spectrometric Method for the Separation and Molecular Weight Determination of Snake Venom Proteins
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作者 杨伯宇 朱大模 +2 位作者 洪群发 孙国强 张玉奎 《Chinese Science Bulletin》 SCIE EI CAS 1994年第20期1702-1705,共4页
Matrix assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI/MS) is a new, powerful analytical tool for the investigation of large biomolecules. Since its inception in 1986 by Koichi Tanaka and ... Matrix assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI/MS) is a new, powerful analytical tool for the investigation of large biomolecules. Since its inception in 1986 by Koichi Tanaka and Franz Hillenkamp separately, MALDI/MS has been successfully applied to the investigation of 展开更多
关键词 MALDI /MS molecular WEIGHT determination of proteinS SNAKE venom.
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