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Physiological roles of mitogen-activated-protein-kinase-activated p38-regulated/activated protein kinase 被引量:8
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作者 Sergiy Kostenko Gianina Dumitriu +1 位作者 Kari Jenssen Lgreid Ugo Moens 《World Journal of Biological Chemistry》 CAS 2011年第5期73-89,共17页
Mitogen-activated protein kinases(MAPKs)are a family of proteins that constitute signaling pathways involved in processes that control gene expression,cell division, cell survival,apoptosis,metabolism,differentiation ... Mitogen-activated protein kinases(MAPKs)are a family of proteins that constitute signaling pathways involved in processes that control gene expression,cell division, cell survival,apoptosis,metabolism,differentiation and motility.The MAPK pathways can be divided into conventional and atypical MAPK pathways.The first group converts a signal into a cellular response through a relay of three consecutive phosphorylation events exerted by MAPK kinase kinases,MAPK kinase,and MAPK.Atypical MAPK pathways are not organized into this three-tiered cascade.MAPK that belongs to both conventional and atypical MAPK pathways can phosphorylate both non-protein kinase substrates and other protein kinases.The latter are referred to as MAPK-activated protein kinases.This review focuses on one such MAPK-activated protein kinase,MAPK-activated protein kinase 5(MK5)or p38-regulated/activated protein kinase(PRAK).This protein is highly conserved throughout the animal kingdom and seems to be the target of both conventional and atypical MAPK pathways.Recent findings on the regulation of the activity and subcellular localization,bona fide interaction partners and physiological roles of MK5/PRAK are discussed. 展开更多
关键词 MITOGEN-activATED protein KINASE p38- regulated/activated protein KINASE Extracellular signalregulated KINASE protein KINASE A SUBCELLULAR localization Phosphorylation protein interaction
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STRUCTURE,MOLECULAR WEIGHT AND BIOACTIVITIES OF(1→3)-β-D-GLUCANS AND ITS SULFATED DERIVATIVES FROM FOUR KINDS OF LENTINUS EDODES 被引量:5
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作者 UnursaikhanSurenjav 张俐娜 +3 位作者 Xiao-juanXu MeiZhang PeterChiKeungCheung Fan-boZeng 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2005年第3期327-336,共10页
Lentinan samples,(1→3)-β-D-glucans containing 4.6-15.2 wt% proteins,coded as L-I_1 L-I_2 L-I_3 and L-I_4(L-I)were isolated from four kinds of Lentinus edodes.These glucans were treated with acetone to remove the pro... Lentinan samples,(1→3)-β-D-glucans containing 4.6-15.2 wt% proteins,coded as L-I_1 L-I_2 L-I_3 and L-I_4(L-I)were isolated from four kinds of Lentinus edodes.These glucans were treated with acetone to remove the protein in orderto obtain free protein glucans coded as LNP-I_1,LNP-I_2.LNP-I_3 and LNP-I_4(LNP-I).The free-protein polysaccharideswere sulfated to give derivatives(S-LNP-I)with degree of substitution(DS)from 0.4-0.8.The structural features andweight-average molecular weight(M_w)of the samples were investigated by using infrared spectroscopy,elemental analysis,^(13)C-NMR,size exclusion chromatography combined with laser light scattering(SEC-LLS)and viscometry.The effects ofstructure and conformation of the polysaccharides on antitumor activities were assayed in vivo(Sarcoma 180 solid tumors)and in vitro(Sarcoma 180,HL-60,MCF-7 and Vero tumors).The results indicated that the predominant species of thesamples L-I and LNP-I in 0.2 mol/L NaCl aqueous solution existed as triple-helical chains with high rigidity and in dimethylsulfoxide(DMSO)as single-flexible chains.Interestingly,the antitumor activities of LNP-I are lower than those of the nativeglucans(L-I),whereas their sulfated derivatives have higher inhibition ratio against Sarcoma 180 than LNP-I.The resultsreveal that the binding of protein,sulfated modification and the triple helix conformation are important factors in theenhancement of the antitumor activities of polysaccharides on the whole. 展开更多
关键词 (1→3)-β-D-glucans Lentinus Edodes Molecular weight protein Sulfated derivative Antitumor activity.
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Structural Basis for the Interaction of 14-3-3<i>β</i>with Tricarboxylic Acid Cycle Intermediate Malate
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作者 Zhiqiang Hou Lijing Su Xiaoyan Liu 《Journal of Biosciences and Medicines》 2017年第8期36-47,共12页
The protein family of 14-3-3(s) has risen to a position of higher importance as an adaptor protein in cell biology. The seven highly conserved human 14-3-3 proteins coordinate diverse cellular processes including apop... The protein family of 14-3-3(s) has risen to a position of higher importance as an adaptor protein in cell biology. The seven highly conserved human 14-3-3 proteins coordinate diverse cellular processes including apoptosis, DNA damage response, protein trafficking, and others. In liver hepatocytes, 14-3-3β binds to Ser196-phosphorilated glucose-responsive carbohydrate response element-binding protein (ChREBP) to inhibit converting excess carbohydrate to fat by regulating the nuclear/cytosol trafficking of ChREBP. Here, we report X-ray crystal structures of homodimeric mammalian 14-3-3β in its apo, Malate-bound forms. The determined apo structure was captured with one monomer in the closed state, whereas the other one had an open conformation. Strikingly, 14-3-3β binds Malate dynamically with a double-closed state, which is distinct from all previously characterized 14-3-3(s) and target ligand-binding modes. Malate docks into a first-time observed cofactor pocket located at the concaved interface of 14-3-3β helices α2, α3, α4 through mainly electrostatic and hydrogen interactions. Such a Tricarboxylic Acid Cycle intermediate Malate bond model might offer a new approach to further analyze insulin-independent 14-3-3/ChREBP pathway of de novo fat synthesis in the liver. 展开更多
关键词 Crystal Structure 14-3-3 protein CHREBP TRANSCRIPTION activation MALATE Malic Acid
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幽门螺杆菌napA基因在乳酸菌中的表达及免疫原性分析 被引量:10
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作者 李建芳 彭正华 +4 位作者 肖红剑 罗娜 杨增福 李健峰 徐维明 《中国生物工程杂志》 CAS CSCD 北大核心 2008年第5期104-110,共7页
实验目的是在乳酸菌中表达幽门螺杆菌(Helicobacter pylori,H.pylori)中性粒细胞激活蛋白(NAP),口服免疫小鼠后检测其免疫原性。在实验中利用了分子克隆技术构建携带nap基因的重组原核表达质粒pNICE:sec-nap,将重组质粒转化乳酸菌NZ9000... 实验目的是在乳酸菌中表达幽门螺杆菌(Helicobacter pylori,H.pylori)中性粒细胞激活蛋白(NAP),口服免疫小鼠后检测其免疫原性。在实验中利用了分子克隆技术构建携带nap基因的重组原核表达质粒pNICE:sec-nap,将重组质粒转化乳酸菌NZ9000株,筛选鉴定阳性菌落,诱导表达的NAP蛋白用SDS-PAGE和Western blot进行鉴定。将雌性ICR(CV级)小鼠随机分为4组,分别用PBS、携带空质粒的乳酸菌、携带pNICE:sec-nap的乳酸菌、灭活的H.pylori灌胃。免疫7次后检测其特异性IgG和IgA的产生。成功扩增了nap基因并构建了重组原核表达质粒pNICE:sec-nap,转化乳酸菌NZ9000后经nisin诱导可表达Mr约17kDa的重组蛋白,表达量约占菌体总蛋白量的9.5%,表达的蛋白能与兔抗H.pylori血清特异性反应,具有良好的免疫原性。携带pNICE:sec-nap质粒的乳酸菌刺激产生的IgG水平明显高于携带空质粒组,与灭活H.pylori组没有明显的差异,但其刺激产生的IgA水平明显高于其他组。结果说明表达NAP蛋白的乳酸菌口服免疫小鼠后,能够刺激小鼠产生特异的IgG和IgA,对幽门螺杆菌疫苗的研究开发具有理论的意义。为乳酸菌作为抗原递送载体的研究和H.pylori口服疫苗的开发提供一定的实验基础。 展开更多
关键词 幽门螺杆菌 乳酸乳球菌 napA基因 中性粒细胞激活蛋白
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幽门螺杆菌napA基因在乳酸菌中的表达及免疫原性分析 被引量:2
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作者 李建芳 彭正华 +4 位作者 肖红剑 罗娜 杨增福 李健锋 徐维明 《中国生物工程杂志》 CAS CSCD 北大核心 2008年第6期77-83,共7页
为在乳酸菌中表达幽门螺杆菌(Helicobacter pylori,H.pylori)中性粒细胞激活蛋白(NAP),口服免疫小鼠后检测其免疫原性。在实验中利用了分子克隆技术构建携带nap基因的重组原核表达质粒pNICE:sec-nap,将重组质粒转化乳酸菌NZ9000株,筛选... 为在乳酸菌中表达幽门螺杆菌(Helicobacter pylori,H.pylori)中性粒细胞激活蛋白(NAP),口服免疫小鼠后检测其免疫原性。在实验中利用了分子克隆技术构建携带nap基因的重组原核表达质粒pNICE:sec-nap,将重组质粒转化乳酸菌NZ9000株,筛选鉴定阳性菌落,诱导表达的NAP蛋白用SDS-PAGE和Western blot进行鉴定。将雌性ICR(CV级)小鼠随机分为4组,分别用PBS、携带空质粒的乳酸菌、携带pNICE:sec-nap的乳酸菌、灭活的H.pylori灌胃。免疫7次后检测其特异性IgG和IgA的产生。成功扩增了nap基因并构建了重组原核表达质粒pNICE:sec-nap,转化乳酸菌NZ9000后经nisin诱导可表达Mr约17kDa的重组蛋白,表达量约占菌体总蛋白量的9.5%,表达的蛋白能与兔抗H.pylori血清特异性反应,具有良好的免疫原性。携带pNICE:sec-nap质粒的乳酸菌刺激产生的IgG水平明显高于携带空质粒组,与灭活H.pylori组没有明显的差异,但其刺激产生的IgA水平明显高于其他组。以上结果说明表达NAP蛋白的乳酸菌口服免疫小鼠后,能够刺激小鼠产生特异的IgG和IgA,对幽门螺杆菌疫苗的研究开发具有理论意义。为乳酸菌作为抗原递送载体的研究和H.pylori口服疫苗的开发提供了一定的实验基础。 展开更多
关键词 幽门螺杆菌 乳酸乳球菌 napA基因 中性粒细胞激活蛋白
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有氧运动与饮食干预对肥胖小鼠睾丸氧化应激的影响
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作者 吕红艳 李涛 +2 位作者 刘姣 王萌 衣雪洁 《中国应用生理学杂志》 CAS CSCD 北大核心 2022年第5期464-469,589,共7页
目的:通过对肥胖小鼠施加有氧运动与饮食干预,探索运动与饮食干预对肥胖小鼠睾丸氧化应激和p38MAPK-NF-κB通路中的作用。方法:随机将17只C57BL/6J小鼠分为正常饮食组(ND),37只分为高脂饮食组(HFD),高脂饮食脂肪占比40%,喂养12周后,HFD... 目的:通过对肥胖小鼠施加有氧运动与饮食干预,探索运动与饮食干预对肥胖小鼠睾丸氧化应激和p38MAPK-NF-κB通路中的作用。方法:随机将17只C57BL/6J小鼠分为正常饮食组(ND),37只分为高脂饮食组(HFD),高脂饮食脂肪占比40%,喂养12周后,HFD组剔除3只肥胖抵抗小鼠,其余34只肥胖造模成功;随后将ND组分为正常饮食对照组(NC,n=8),正常饮食运动组(NE,n=9),肥胖高脂饮食对照组(OC,n=8),肥胖高脂饮食运动组(OE,n=9),肥胖正常饮食组(ONC,n=8),肥胖正常饮食运动组(ONE,n=9),各组继续饲养8周,其中NE、OE和ONE组以速度20 m/min,60 min/d,6 d/week,进行8周跑台运动,末次运动后36~40 h取血和睾丸组织,ELISA检测血清睾酮和睾丸氧化应激(MDA、T-SOD、T-AOC)水平,RT-PCR和Western blot检测睾丸p38MAPK-NF-κB水平。结果:与NC组比较,OC组小鼠体脂参数、睾丸MDA和睾丸p38MAPK-NF-κB mRNA和蛋白水平明显升高(P<0.01),睾丸SOD、睾丸系数和血睾酮明显降低(P<0.01);NE组小鼠体脂参数明显降低(P<0.05),血清睾酮明显升高(P<0.01)。与OC组比较,OE组小鼠体脂参数、睾丸MDA和睾丸p38MAPK-NF-κB mRNA和蛋白水平明显降低(P<0.05或0.01),睾丸SOD和血睾酮水平明显升高(P<0.01);ONC组小鼠体脂参数、睾丸MDA和睾丸p38MAPK-NF-κB mRNA和蛋白水平明显降低(P<0.01),睾丸SOD水平和睾丸系数明显升高(P<0.05);ONE组小鼠体脂参数、睾丸MDA和睾丸p38MAPK-NF-κB mRNA和蛋白水平明显降低(P<0.01),睾丸SOD、睾丸系数和血睾酮水平明显升高(P<0.01)。结论:肥胖引起小鼠睾丸发生氧化应激,上调睾丸p38MAPK-NF-κB水平,并降低血睾酮水平;运动、饮食和运动×饮食干预均能通过降低体脂,改善睾丸氧化应激,下调睾丸p38MAPK-NF-κB水平。 展开更多
关键词 高脂饮食 运动和饮食干预 氧化应激 p38丝裂原活化蛋白激酶(p38 mitogen activated protein kinase p38MAPK) 核转录因子-κB(nuclear factor kappa-B NF-κB) 睾酮 小鼠
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Association of ALOX5AP and PDE4D with the risk of lacunar infarct in people from Jiangsu Province,China 被引量:2
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作者 Hong Cheng Qingwen Jin +3 位作者 Lixin Li Xinsheng Ding Xinjian Song Yanying Zeng 《Neural Regeneration Research》 SCIE CAS CSCD 2011年第12期935-940,共6页
The genes for 5-1ipoxygenase activating protein (ALOX5AP) and phosphodiesterase 4D (PDE4D) have been demonstrated as susceptibility genes for lacunar in the Icelandic and Pakistani populations, but little is known... The genes for 5-1ipoxygenase activating protein (ALOX5AP) and phosphodiesterase 4D (PDE4D) have been demonstrated as susceptibility genes for lacunar in the Icelandic and Pakistani populations, but little is known about the role of these genes in Chinese populations. The present study utilized polymerase chain reaction and ligase detection reaction to detect single nucleotide polymorphisms (SNPs) in 280 consecutive stroke patients and 258 unrelated population-based controls from Nanjing, Jiangsu Province, China. The allele frequency, genotypes, and haplotypes of the two SNPs (rs456009 and rs966221) in PDE4D were similar between the two groups. However, A allele frequency of rs4073259 (A/G) and rs4769055 (A/C) in the ALOX5AP gene exhibited differences in two groups, and especially the haplotype of the SNP was significantly different between the two groups. Results suggested that the ALOX5AP gene might be involved in lacunar infarct, while PDE4D gene was not a risk factor for lacunar infarct in individuals from Jiangsu Province, China. 展开更多
关键词 lacunar infarct 5-1ipoxygenase activating protein phosphodiesterase 4D single nucleotide polymorphism polymerase chain reaction ligase detection reaction gene polymorphism
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幽门螺杆菌napA基因的克隆表达及免疫原性研究
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作者 张莹丹 杨旭 +4 位作者 彭正华 何春艳 陈阳 徐维明 李健峰 《云南大学学报(自然科学版)》 CAS CSCD 北大核心 2007年第S3期403-407,共5页
采用PCR方法扩增幽门螺杆菌napA基因片段并克隆至原核表达载体pET28a获得重组质粒pET28a-nap.将重组质粒转化E.coli BL21(DE3)表达菌后经IPTG诱导表达融合蛋白NAP,相对分子质量约为18ku,表达量约占菌体蛋白总量的40%.融合蛋白经纯化后... 采用PCR方法扩增幽门螺杆菌napA基因片段并克隆至原核表达载体pET28a获得重组质粒pET28a-nap.将重组质粒转化E.coli BL21(DE3)表达菌后经IPTG诱导表达融合蛋白NAP,相对分子质量约为18ku,表达量约占菌体蛋白总量的40%.融合蛋白经纯化后获得纯度为95%以上的重组蛋白,Western blot分析其能与幽门螺杆菌抗血清特异性反应.与佐剂CpG ODN联合口服免疫小鼠后,可有效诱导免疫应答,产生高水平的IgG,与未加佐剂组相比具有显著性差异(t=7.095,P<0.01).以上结果说明融合蛋白NAP联合佐剂CpG ODN经口服免疫可有效诱导免疫应答.NAP可作为幽门螺杆菌口服疫苗候选抗原. 展开更多
关键词 幽门螺杆菌 napA基因 中性粒细胞激活蛋白
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