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Cooperation between matrix metalloproteinases and the plasminogen activator-plasmin system in tumor progression. 基质金属蛋白酶与纤溶酶原激活物-纤溶酶系统在肿瘤进展中的协同作用。
Enzyme & protein Pub Date : 1996-01-01 DOI: 10.1159/000468617
Y A DeClerck, W E Laug
{"title":"Cooperation between matrix metalloproteinases and the plasminogen activator-plasmin system in tumor progression.","authors":"Y A DeClerck,&nbsp;W E Laug","doi":"10.1159/000468617","DOIUrl":"https://doi.org/10.1159/000468617","url":null,"abstract":"<p><p>Several classes of extracellular matrix (ECM)-degrading proteases have been shown to play an important role in tumor invasion and metastasis. Among them, the matrix metalloproteinases (MMPs) and the plasminogen activator (PA)-plasmin system have been the focus of numerous studies. However, few of those have examined the interaction of these two classes of proteases during tumor progression and their specific roles in this complex process have remained unclear. In this article, comparative information on the structure, function, and regulation of these two classes of proteases is reviewed and their interaction on various levels is discussed. This review shows that MMPs and the PA-plasmin system closely cooperate to achieve optimal degradation of the ECM during the invasive and metastatic process.</p>","PeriodicalId":11854,"journal":{"name":"Enzyme & protein","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468617","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19766946","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 96
Urokinase plasminogen activator as a predictor of aggressive disease in breast cancer. 尿激酶纤溶酶原激活剂作为乳腺癌侵袭性疾病的预测因子
Enzyme & protein Pub Date : 1996-01-01 DOI: 10.1159/000468618
M J Duffy, C Duggan, T Maguire, K Mulcahy, P Elvin, E McDermott, J J Fennelly, N O'Higgins
{"title":"Urokinase plasminogen activator as a predictor of aggressive disease in breast cancer.","authors":"M J Duffy,&nbsp;C Duggan,&nbsp;T Maguire,&nbsp;K Mulcahy,&nbsp;P Elvin,&nbsp;E McDermott,&nbsp;J J Fennelly,&nbsp;N O'Higgins","doi":"10.1159/000468618","DOIUrl":"https://doi.org/10.1159/000468618","url":null,"abstract":"<p><p>Urokinase plasminogen activator (uPA) is a multifunctional protein involved in both extracellular proteolysis and signal transduction. uPA usually mediates its actions while attached to a membrane-bound receptor, termed uPAR. In this study, uPA and its receptor were measured at both protein and mRNA levels in breast cancer. At both levels, concentrations of uPA were significantly correlated with those for uPAR. uPA levels also correlated significantly with cathepsin B and cathepsin D but not with cathepsin L, MMP-8 or MMP-9 levels. Irrespective of the cut-off point used (e.g., median, tertile or quartile values), uPA was a significant prognostic marker for breast cancer.</p>","PeriodicalId":11854,"journal":{"name":"Enzyme & protein","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468618","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19766947","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 36
Angiogenesis: a paradigm for balanced extracellular proteolysis during cell migration and morphogenesis. 血管生成:在细胞迁移和形态发生过程中平衡的细胞外蛋白水解的范例。
Enzyme & protein Pub Date : 1996-01-01 DOI: 10.1159/000468622
M S Pepper, R Montesano, S J Mandriota, L Orci, J D Vassalli
{"title":"Angiogenesis: a paradigm for balanced extracellular proteolysis during cell migration and morphogenesis.","authors":"M S Pepper,&nbsp;R Montesano,&nbsp;S J Mandriota,&nbsp;L Orci,&nbsp;J D Vassalli","doi":"10.1159/000468622","DOIUrl":"https://doi.org/10.1159/000468622","url":null,"abstract":"<p><p>Extracellular proteolysis is required for matrix degradation and the regulation of cytokine activity during angiogenesis, and this is dependent on a cohort of proteases and protease inhibitors produced by endothelial and nonendothelial cells. The plasminogen activator (PA)/plasmin system has been extensively investigated in these processes, and descriptive studies have demonstrated that urokinase-type PA (uPA), uPA receptor (uPAR) and PA inhibitor-1 (PAI-1) are expressed by endothelial cells during angiogenesis in vivo. In vitro studies have led to the notion that normal capillary morphogenesis is dependent on a protease-antiprotease equilibrium. These findings are discussed in the context of recent observations on uPA-, uPAR-, PAI-1 and plaminogen-deficient mice, in which developmental and physiological angiogenesis appear to occur normally. This has led to a reevaluation of the role of the PA/plasmin system during angiogenesis. In particular, these observations raise the possibility that the role of this system may be limited to situations in which endothelial cells encounter and must degrade fibrin in order to form new capillary sprouts.</p>","PeriodicalId":11854,"journal":{"name":"Enzyme & protein","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468622","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19768265","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 225
The integrity of thiol groups is essential for catalytic efficiency of rat liver cholesterol ester hydrolase either in microsomal membranes or after solubilization. 巯基的完整性对大鼠肝脏胆固醇酯水解酶在微粒体膜或溶解后的催化效率至关重要。
Enzyme & protein Pub Date : 1996-01-01 DOI: 10.1159/000468638
M López de Heredia, S Cristóbal, M L Hernández, M J Martínez, B Ochoa
{"title":"The integrity of thiol groups is essential for catalytic efficiency of rat liver cholesterol ester hydrolase either in microsomal membranes or after solubilization.","authors":"M López de Heredia,&nbsp;S Cristóbal,&nbsp;M L Hernández,&nbsp;M J Martínez,&nbsp;B Ochoa","doi":"10.1159/000468638","DOIUrl":"https://doi.org/10.1159/000468638","url":null,"abstract":"<p><p>Neutral cholesterol ester hydrolase from rat liver microsomes was inactivated in a dose and time-dependent manner by classical sulphydryl-reacting reagents such as p-hydroxymercuribenzoic acid, 5,5'-dithio-bis-(2-nitrobenzoic acid), N-ethylmaleimide, or iodoacetate. The concentrations at which half-maximal inhibition of the native microsomal cholesterol ester hydrolase occurred (IC50) were 15, 68, and 370 mumol/l and 68 mmol/l, respectively. Only partial reactivation of the enzyme was observed under excess dithiothreitol or mercaptoethanol treatment. The stimulation of cholesterol ester hydrolase by the metal ions Ca2+ and Mg2+ was dependent on the integrity of the thiol groups. Solubilization of cholesterol ester hydrolase from membranes preserved its sensitivity towards sulphydryl reagents and thiols, as well as its ability to be activated by Ca2+ and Mg2+. Dithiothreitol, mercaptoethanol, and Ca2+ and Mg2+ provided total protection of the enzyme against inactivation by thiol-reacting reagents. The results indicate that one or more thiol groups are either at the active centre of the native and solubilized forms of rat liver microsomal cholesterol ester hydrolase or are sufficiently near, to interfere with the catalysis when they are reacted.</p>","PeriodicalId":11854,"journal":{"name":"Enzyme & protein","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468638","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"20196919","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
The role of stromelysin-1 in stromal-epithelial interactions and cancer. 基质溶素-1在基质-上皮相互作用和癌症中的作用。
Enzyme & protein Pub Date : 1996-01-01 DOI: 10.1159/000468624
J F Wiesen, Z Werb
{"title":"The role of stromelysin-1 in stromal-epithelial interactions and cancer.","authors":"J F Wiesen,&nbsp;Z Werb","doi":"10.1159/000468624","DOIUrl":"https://doi.org/10.1159/000468624","url":null,"abstract":"<p><p>Stromelysin-1 was one of the first proteinases found to be associated with cancer. In this review we describe the role of stromelysin-1 in normal mammary gland involution. When stromelysin-1 is overexpressed in transgenic mice the mammary gland undergoes precocious involution and is predisposed to forming a reactive stroma resembling that of a wound site or a tumor. Stromelysin-1 may act as an oncogene because transgenic mice expressing an active form of the enzyme develop mammary tumors. These observations suggest that stromelysin-1 and other matrix metalloproteinases may be useful targets for therapeutic intervention in cancer.</p>","PeriodicalId":11854,"journal":{"name":"Enzyme & protein","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000468624","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19768267","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 22
Proteasomes. Multicatalytic proteinase complexes. 水解酶。多催化蛋白酶复合物。
Enzyme & protein Pub Date : 1994-12-13 DOI: 10.1159/ISBN.978-3-318-06186-4
S. Wilk
{"title":"Proteasomes. Multicatalytic proteinase complexes.","authors":"S. Wilk","doi":"10.1159/ISBN.978-3-318-06186-4","DOIUrl":"https://doi.org/10.1159/ISBN.978-3-318-06186-4","url":null,"abstract":"Studies on the yeast proteasome uncover its basic structural features and multiple in vivo functions, W. Hilt et al characterization of proteasomes isolated from rat liver, A.J. Rivett lobster muscle proteasome and the degradations of myofibrillar proteins, D.L. Mykles subunit stoichiometry of human proteasomes, K.B. Hendil et al in vitro activation of the 20S proteasome, B. Dahlmann et al modulation of the multicatalytic proteinase complex by lipids, interconversion and proteolytic processing, P. Arizti et al catalytic components of the bovine pituitary multicatalytic proteinase complex (proteasome), C. Cardozo synthetic inhibitors of the multicatalytic proteinase complex (proteasome), S. Wilk and M.E. Figueiredo-Pereira characterization of mouse proteasome subunit MC3 and identification of proteasome subtypes with different cleavage characteristics - proteasome subunits, proteasome subpopulations, A. Seelig et al biochemical purification of distinct proteasome subsets, M.G. Brown and J.J. Monaco. (Part Contents).","PeriodicalId":11854,"journal":{"name":"Enzyme & protein","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1994-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89789993","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Kinetics of irreversible inhibition of yeast alcohol dehydrogenase during modification by o-phthaldehyde. 邻苯二醛修饰酵母醇脱氢酶的不可逆抑制动力学。
Enzyme & protein Pub Date : 1994-01-01 DOI: 10.1159/000474985
W P Le, S X Yan, M Q Huang, Y X Zhang, H M Zhou
{"title":"Kinetics of irreversible inhibition of yeast alcohol dehydrogenase during modification by o-phthaldehyde.","authors":"W P Le,&nbsp;S X Yan,&nbsp;M Q Huang,&nbsp;Y X Zhang,&nbsp;H M Zhou","doi":"10.1159/000474985","DOIUrl":"https://doi.org/10.1159/000474985","url":null,"abstract":"<p><p>The kinetic theory of the substrate reaction during irreversible inhibition of enzyme activity described previously has been applied to a study on the kinetics of the course of inactivation of yeast alcohol dehydrogenase (YADH) by o-phthaldehyde (OPTA). The microscopic constants for the reaction of the inactivators with the free enzyme and with the enzyme-substrate complexes were determined. The inactivation is a monophasic pseudo-first-order reaction with OPTA. The apparent rate constant A is independent of the OPTA concentration, indicating that the inactivation is a noncomplexing inhibition. The marked protective effect of substrates on the inactivation of YADH by OPTA has been observed. This result suggests that the modification of the enzyme by OPTA may occur at the active site.</p>","PeriodicalId":11854,"journal":{"name":"Enzyme & protein","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1994-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000474985","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19569781","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Yeast porphobilinogen deaminase also forms enzyme-pyrrole intermediates. 酵母卟啉原脱氨酶也形成酶-吡咯中间体。
Enzyme & protein Pub Date : 1994-01-01 DOI: 10.1159/000475000
S Correa Garcia, M V Rossetti, M Bermudez Moretti, A M Batlle
{"title":"Yeast porphobilinogen deaminase also forms enzyme-pyrrole intermediates.","authors":"S Correa Garcia,&nbsp;M V Rossetti,&nbsp;M Bermudez Moretti,&nbsp;A M Batlle","doi":"10.1159/000475000","DOIUrl":"https://doi.org/10.1159/000475000","url":null,"abstract":"<p><p>The enzyme porphobilinogen deaminase (PBG deaminase, EC 4.3.1.8) catalyzes the condensation of four molecules of PBG to give the linear tetrapyrrol, hydroxymethylbilane. It has been shown that this enzyme forms stable mono-, di-, tri- and tetrapyrrole-enzyme covalent complexes. When the enzyme, partially purified in the absence or presence of phenylmethylsulfonyl fluoride (PMSF) and preincubated with PBG, was applied on DEAE-cellulose columns, three peaks with PBG deaminase activity were detected. Using Ehrlich's reagent, it was found that the active peaks corresponded to mono-, di- and tri-pyrrylmethane-enzyme complexes. Therefore, the mechanism of action of PBG deaminase from Saccharomyces cerevisiae also involves the sequential addition of four PBG units, leading to the formation of the enzyme-substrate intermediate complexes, as has already been described for the same enzyme from other sources.</p>","PeriodicalId":11854,"journal":{"name":"Enzyme & protein","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1994-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000475000","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19765118","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Pig platelet acidic carboxypeptidases. 猪血小板酸性羧肽酶。
Enzyme & protein Pub Date : 1994-01-01 DOI: 10.1159/000475002
H Ostrowska
{"title":"Pig platelet acidic carboxypeptidases.","authors":"H Ostrowska","doi":"10.1159/000475002","DOIUrl":"https://doi.org/10.1159/000475002","url":null,"abstract":"<p><p>Pig platelet acidic carboxypeptidases hydrolyzed only N-blocked dipeptides with bulky aromatic and aliphatic hydrophobic amino acids. The optimum hydrolysis of these substrates was at pH 5.0. The main acidic carboxypeptidase in pig platelet lysate was lysosomal carboxypeptidase A (1CPA), which hydrolyzed Cbz-Phe-Ala at the highest rate. A lower activity of this enzyme was found on Cbz-Glu-Tyr and Cbz-Glu-Phe. 1CPA also hydrolyzed Cbz-Glu-Tyr at pH 3.5. No activity of lysosomal carboxypeptidase B in platelet lysate was detectable using Bz-Gly-Arg. Pig platelet acidic carboxypeptidase hydrolyzed Cbz-Pro-Phe and Cbz-Pro-Ala, which are specific substrates of lysosomal prolylcarboxypeptidase, more slowly. The incubation of platelet lysate with plasma did not influence the rate of hydrolysis of Cbz-Glu-Tyr, whereas no hydrolysis of Cbz-Pro-Phe was observed.</p>","PeriodicalId":11854,"journal":{"name":"Enzyme & protein","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1994-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000475002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19765121","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Diagnostic significance of urinary enzymes for diabetes mellitus and hypertension. 尿酶对糖尿病和高血压的诊断意义。
Enzyme & protein Pub Date : 1994-01-01 DOI: 10.1159/000474984
N Ishii, Z Ogawa, H Itoh, H Ikenaga, T Saruta
{"title":"Diagnostic significance of urinary enzymes for diabetes mellitus and hypertension.","authors":"N Ishii,&nbsp;Z Ogawa,&nbsp;H Itoh,&nbsp;H Ikenaga,&nbsp;T Saruta","doi":"10.1159/000474984","DOIUrl":"https://doi.org/10.1159/000474984","url":null,"abstract":"<p><p>In order to evaluate tubular damage in diabetic patients, the activity of renal proximal tubule derived enzymes excreted in 24-hour urine were recorded in 5 groups as follows: (i) 48 noninsulin-independent diabetic patients with normal renal function and a urinary albumin excretion rate within the normal range; (ii) 45 noninsulin-dependent diabetic patients with normal renal function and a high urinary albumin level; (iii) 26 noninsulin-dependent diabetic patients with renal failure; (iv) 40 patients with essential hypertension and normal renal function, and (v) 48 normal control subjects. Regardless of whether cases were noninsulin-dependent diabetics with normal or high urinary albumin excretion rate or cases with renal dysfunction, urinary dipeptidyl aminopeptidase IV and N-acetyl-beta-D-glucosaminidase excretions were significantly higher than in healthy subjects, and urinary gamma-glutamyl transpeptidase excretion was significantly lower than in healthy subjects. No significant changes in urinary enzyme excretions showed specific variations in the essential hypertensive patients. These results suggest that there is tubular damage in the early stages of noninsulin-dependent diabetic patients with normal renal function and normal urinary albumin excretion rate. Detection of urinary excretion of dipeptidyl aminopeptidase IV, N-acetyl-beta-D-glucosaminidase and gamma-glutamyl transpeptidase may be especially useful for the early diagnosis of diabetic nephropathy.</p>","PeriodicalId":11854,"journal":{"name":"Enzyme & protein","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1994-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000474984","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19569778","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 20
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