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1.
半胱氨酸蛋白酶(CP)是广泛存在于动物和植物以及寄生虫中的一类含有半胱氨酸残基的蛋白水解酶,是蛋白酶家族中最重要的成员之一.目前,对人CP的研究宅要集中在凋亡和肿瘤两个方面,而对寄生虫CP的研究则相对比较广泛.  相似文献   

2.
家蚕杆状病毒半胱氨酸蛋白酶基因的序列分析及表达   总被引:1,自引:1,他引:0  
通过PCR扩增技术克隆了家蚕核型多角体病毒 (BombyxmoriNuclearPolyhedrosisVirus ,BmNPV)ZJ8株的半胱氨酸蛋白酶 (cysteineproteinase ,CP)基因 (BmNPVZJ8 CP)。序列分析表明 ,该蛋白酶基因的ORF为 972个核苷酸 ,编码 32 3个氨基酸。同源性分析表明 ,BmNPVZJ8 CP在DNA水平上与其它来源的CP具有较高的同源性 ,根据已知的杆状病毒半胱氨酸蛋白酶序列构建了该基因的进化树 ,发现BmNPVZJ8 CP与人的木瓜蛋白酶超家族的CP在同一进化分支上 ,与BmNPV T3株、AcNPV的半胱氨酸蛋白酶基因的核苷酸同源性最高。该基因在大肠杆菌中表达的产物对大肠杆菌具有生理毒性 ,从而限制了该基因的表达。  相似文献   

3.
植物半胱氨酸蛋白酶研究进展   总被引:6,自引:0,他引:6  
半胱氨酸蛋白酶是植物中重要的蛋白酶家族之一,广泛参与种子萌发、幼苗发育,胁迫响应和组织分化衰老等过程.针对这一重要特性,分别综述了半胱氨酸蛋白酶的分类、结构、编码基因和表达调节方式及其在植物生长过程中的作用.  相似文献   

4.
家蚕(Bombyx mori)作为鳞翅目模式昆虫,较早开展了组织蛋白酶研究,其中以对家蚕半胱氨酸蛋白酶(cysteine protease)的研究居多。半胱氨酸蛋白酶参与了家蚕生长发育、蜕皮变态和免疫调节等生命活动过程。本文重点综述近几年国内外学者在家蚕半胱氨酸蛋白酶分类、基因表达特征、生物学功能研究方面取得的新进展,并简要阐述对家蚕半胱氨酸蛋白酶研究的主要方面。  相似文献   

5.
蜱作为体表吸血节肢动物,可通过采食宿主血液传播多种病原体,是一种重要媒介。半胱氨酸蛋白酶是一类分布广泛具有一定保守性的蛋白酶,在蜱生理学中发挥重要作用。本文对蜱半胱氨酸蛋白酶的研究进展进行了综述,重点介绍了组织蛋白酶、天冬酰胺内肽酶和半胱天冬氨酸蛋白酶,及参与自噬反应的半胱氨酸蛋白酶的功能及相互作用。  相似文献   

6.
半胱氨酸蛋白酶抑制剂是一类在进化相关的蛋白质,能够抑制半胱氨酸蛋白酶类的活性。根据氨基酸序列和一级结构特征,将半胱氨酸蛋白酶抑制剂分为stefins家族,cystatins家族,kininogens家族和fetuin家族四个亚家族。本文通过结合半胱氨酸蛋白酶抑制剂功能的研究进展,对吸虫、绦虫、线虫和原虫半胱氨酸蛋白酶抑制剂的结构、种类、免疫调节和免疫逃避功能进行综述,以期对寄生虫半胱氨酸蛋白酶抑制剂的应用和深入研究提供参考。  相似文献   

7.
半胱氨酸蛋白酶基因在家蚕杆状病毒表达系统中的表达   总被引:2,自引:0,他引:2  
为了探讨杆状病毒的致病机理、改善杆状病毒表达系统的表达效率 ,将来源于家蚕核型多角体病毒ZJ8株的半胱氨酸蛋白酶 (cystenineprotease,CP)基因克隆到转移载体pVL 1393上 ,获得重组转移载体pVL cp ,与线性化的Bm BacPAK6病毒DNA共转染家蚕Bm 5贴壁细胞。通过蓝白斑筛选、纯化后得到的重组病毒经PCR鉴定证明 ,cp基因已被正确导入 ,注射感染家蚕 5龄幼虫 12 0h后表达产物活性达到最高。对表达产物进行SDS PAGE及酶活力分析 ,检测到半胱氨酸蛋白酶在家蚕生物反应器中的表达 ,其表达量约为 16 0 0U/mL。  相似文献   

8.
组织蛋白酶(cathepsin,CTS)是半胱氨酸蛋白酶家族的主要成员,包括组织蛋白酶B(CTSB)、组织蛋白酶S(CTSS)和组织蛋白酶C(CTSC)等,它们是一类主要存在于溶酶体中的细胞内肽键水解酶.对组织蛋白酶的研究可以追溯到上世纪上半叶,CTSC是第一个被纯化的蛋白酶.但之后的几十年相关研究发展缓慢,直至上世纪80年代,组织蛋白酶B、H、L才被鉴定并测序.  相似文献   

9.
试验旨在研究蛋白酶在低蛋白饲粮中对肉鸡生长性能、屠宰性能、养分消化率、氨基酸消化率和消化酶活性的影响.将324只1日龄AA白羽肉仔鸡按照体重相近、公母各半原则随机分为3组,每组6个重复,每个重复18只鸡.对照组饲粮前期粗蛋白质(CP)23%、后期CP 20%;低蛋白组饲粮前期CP 21%、后期CP 18%;低蛋白加酶组...  相似文献   

10.
蜱是以吸血为生的体外寄生虫,能传播多种病原体。控制蜱的传统方法是使用杀虫剂,但会产生药物残留等问题。为了找到控制蜱及蜱传病的新方法,必须在分子水平上了解蜱的相关生理过程。蜱半胱氨酸蛋白酶抑制分子是一类抗蛋白酶分子,主要作用于半胱氨酸蛋白酶的抑制调控。论文介绍了蜱半胱氨酸蛋白酶抑制分子的结构和分类,以及在蜱的吸血、血液消化、蜱的先天免疫及对宿主免疫调节等生理过程的重要作用,同时也综述了半胱氨酸蛋白酶抑制分子具有抗寄生虫和抗癌的作用,为全面了解蜱半胱氨酸蛋白酶抑制分子提供参考。  相似文献   

11.
OBJECTIVE: To evaluate the cytopathic effects of Tritrichomonas foetus and a purified cysteine protease (ie, CP30) of T foetus on cultured bovine uterine epithelial cells (BUECs) in vitro. SAMPLE POPULATION: 10 reproductive tracts were obtained from late-term bovine fetuses at a commercial abattoir. PROCEDURE: An in vitro culture system of BUECs was developed to study the cytopathic effects of T foetus and purified CP30 of T foetus on host cells. Cytotoxicity of T foetus or CP30 on exposed BUECs was determined. Fluorescence microscopy and flow cytometry analyses were used to detect apoptosis. A fluorometric assay was used to detect BUEC caspase 3 activation. The CP inhibitor E-64 and a caspase inhibitor were used to inhibit apoptosis. RESULTS: Cytopathic effects were observed in BUECs treated with parasites or CP30 and were concentration and time dependent. The BUECs underwent apoptosis in the presence of parasites or CP30. The specific CP inhibitor E-64 abolished the induction of apoptosis in BUECs by CP30. The caspase inhibitor reduced the amount of apoptosis in BUECs. CONCLUSIONS AND CLINICAL RELEVANCE: T foetus and its CP30 induce apoptosis in cultured BUECs in vitro. Induction of apoptosis by CP30 is correlated with protease activity. Endometrial cell death as a result of a T foetus infection is likely to be more important in mediating infertility than a direct effect on the conceptus. Provoking an apoptotic reaction in the host may mitigate an inflammatory reaction or immune response and therefore favor survival of the parasite in a chronic infection.  相似文献   

12.
Taenia solium metacestode, a larval pork tapeworm, is a causative agent of neurocysticercosis, one of the most common parasitic diseases in the human central nervous system. In this study, we identified a cDNA encoding for a cathepsin L-like cysteine protease from the T. solium metacestode (TsCL-1) and characterized the biochemical properties of the recombinant enzyme. The cloned cDNA of 1216 bp encoded 339 amino acids with an approximate molecular weight of 37.6 kDa which containing a typical signal peptide sequence (17 amino acids), a pro-domain (106 amino acids), and a mature domain (216 amino acids). Sequence alignments of TsCL-1 showed low sequence similarity of 27.3-44.6 to cathepsin L-like cysteine proteases from other helminth parasites, but the similarity was increased to 35.9-55.0 when compared to mature domains. The bacterially expressed recombinant protein (rTsCL-1) did not show enzyme activity; however, the rTsCL-1 expressed in Pichia pastoris showed typical biochemical characteristics of cysteine proteases. It degraded human immunoglobulin G (IgG) and bovine serum albumin (BSA), but not collagen. Western blot analysis of the rTsCL-1 showed antigenicity against the sera from patients with cysticercosis, sparganosis or fascioliasis, but weak or no antigenicity against the sera from patients with paragonimiasis or clonorchiasis.  相似文献   

13.
Rabbit cysticercosis, caused by the larval stage of Taenia pisiformis, is a serious parasitic disease of rabbits. It was reported that some cysteine peptidases have potential roles in the pathogenesis of various parasitic infections. To investigate the biochemical characteristics and roles in the pathogenesis/host-invasion of cysteine peptidases, a cDNA sequence encoding for a cathepsin L-like cysteine protease (TpCP) was cloned and identified from the T. pisiformis metacestodes. This sequence was 1220 bp in its length, which included a 1017 bp open reading frame encoding a 339 amino acid peptide. Multiple sequence alignments revealed a 28.9–88.5% similarity with cathepsin L-like cysteine proteases from other helminth parasites and mammals. The recombinant TpCP expressed in Escherichia coli did not show the proteolytic activity by zymography gel assay. However, the TpCP expressed in Pichia pastoris had typical biochemical activities that could hydrolyze rabbit immunoglobulin G, bovine serum albumin and fibronectin. Substrate studies indicated pronounced cleavage of Z-Phe-Arg-AMC. This activity was sensitive to cysteine protease inhibitor E-64 and immunohistochemistry results also indicated that TpCP was distributed as an intense positive reaction in the bladder wall. Our results gave us insights into future studies of TpCP's roles in the infection.  相似文献   

14.
The effects of supplementation with cellulase, xylanase, pectinase, hemicellulase, glucanase, phytase and protease of microbial origin on digestibility of crude protein (CP) and dry matter (DM) of soybean meal in vitro were examined in the present study. Changes in viscosity during in vitro digestion were also examined as an index of carbohydrate digestibility. Hemicellulase and all enzyme combinations without protease showed significant improvement of CP digestibility. Cellulase, xylanase, phytase and glucanase tended to improve CP digestibility. Dry matter digestibility was improved significantly by pectinase and all enzyme combinations. Cellulase and phytase tended to improve DM digestibility. Crude protein and DM digestibilities were the highest when all the enzymes except protease were added. Protease, cellulase, pectinase, xylanase, glucanase and hemicellulase significantly reduced viscosity, while phytase had no effect on viscosity. Viscosity was increased unexpectedly when all the enzymes were added. These results strongly suggest that a combination of carbohydrases improves the CP and DM digestibility of soybean meal while protease inhibits the actions of these enzymes. The present study also suggests that viscosity is not always a good index of digestibility. Moreover, excluding the protease from commercial crude enzyme preparations may improve digestibility.  相似文献   

15.
To control parasitic disease in cattle, one first has to determine what parasites he or she is trying to control--nuisance and biting flies in a milking parlor or ticks on range cattle? The determination may be based on geographic location, class of cattle, and their management. After determining what is there, then if the numbers are sufficient, justify treatment. Each livestock producer has a different array of parasites with which to deal, and in some circumstances, parasitic disease is below the economic threshold. Others may have occasional clinical disease associated with parasites, but most have situations in which the potential of economic loss is high enough to justify control.  相似文献   

16.
大多数体内寄生虫的生存必须依赖糖酵解途径将葡萄糖代谢为乳酸以提供能量。乳酸脱氢酶(lactate dehydrogenase, LDH)是糖酵解途径的末端酶,催化丙酮酸还原为乳酸及乳酸氧化为丙酮酸的可逆反应,与寄生虫生存密切相关。研究表明,各种寄生虫LDH在理化性质和分子结构方面均有独特的特性,是良好的诊断分子和潜在的药物作用靶标。对寄生虫LDH功能的研究,对于促进寄生虫病诊断、疫苗研究以及新抗虫药物的研发具有重要意义。本文对国内外寄生虫LDH的研究现状进行了综述。  相似文献   

17.
A 26-28 kDa protease was isolated from Fasciola gigantica adult worms by a two-stage purification process of column chromatography in a Sephacryl S-200 column and affinity chromatography in an L-phenylalanine-agarose column. This protease is a cysteine (thiol) proteinase with an optimum pH of 4.5 and is not inhibited by anti F. gigantica immunoglobulin G. The enzyme was inhibited by protease inhibitors known to inhibit cysteine proteases but not by metallo-, aspartate or serine protease inhibitors. The effect of several protease inhibitors and anti-F, gigantica IgG was also assessed on the total proteolytic activity of F. gigantica. There appears to be a preponderance of cysteine protease activity in F. gigantica and there was a significant inhibition of total proteolytic activity by anti-F. gigantica IgG.  相似文献   

18.
Proteases catalyse the cleavage of internal peptide bonds within peptides and proteins. They are classified into four major classes and are involved in a broad range of eukaryotic processes. Proteases have also been found to play a number of critical roles in the virulence of pathogenic agents, particularly of nematode parasites. Parasitic proteases are involved in different aspects of host-parasite interactions. They facilitate the invasion of host tissues and allow nutrition as well as the survival of the parasite in its host. Proteases also participate in the parasite's evasion from the host's immune response. The functional diversity and complexity of these enzymes are described in this review, with a particular focus on the principally identified proteases of four helminths: Schistosoma sp., Fasciola sp., Taenia sp. and Haemonchus sp. Some of these proteases, especially the cysteine proteases secreted by the parasitic trematode Fasciola hepatica, have been successfully tested in experimental immunodiagnosis. Proteases identified in different parasites are currently under study for a use as recombinant vaccines. In this respect, proteases are proposed as major potential targets for immunotherapy and chemotherapy against parasitic diseases.  相似文献   

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