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从库氏棘阿米巴中克隆半胱氨酸蛋白酶基因。

Cloning of a cysteine proteinase gene from Acanthamoeba culbertsoni.

作者信息

Yun H C, Kim K Y, Park S Y, Park S K, Park H, Hwang U W, Hong K M, Ryu J S, Min D Y

机构信息

Department of Parasitology, College of Medicine, Wonkwang University, Iksan, Korea.

出版信息

Mol Cells. 1999 Oct 31;9(5):491-6.

Abstract

Free living amoeba, including pathogenic Acanthamoeba culbertsoni, are widely distributed in soil and fresh water. It has been found that cysteine proteinases are more active in pathogenic strains of amoeba whereas serine proteinases are found in both pathogenic and nonpathogenic strains. Cysteine proteinases thus play important roles in the pathogenesis of several parasitic infections and have been proposed as targets for the structure-based strategy of drug design. As the first step toward applying this strategy to design inhibitors as antiparasitic agents for A. culbertsoni, we isolated and sequenced the full length clone of a cysteine proteinase gene from A. culbertsoni by performing reverse transcription-polymerase chain reaction (RT-PCR) with degenerate oligonucleotide primers derived from conserved cysteine proteinase sequences. The 5' and the 3' regions of the cysteine proteinase gene were amplified using the PCR protocol for the rapid amplification of cDNA ends (RACE). It has an open reading frame of 1359 bp. The deduced amino acid sequence has the sequence homology with the cysteine proteinase genes of Paragonimus westermani metacercaria, Schistosoma mansoni, human cathepsin L and Fasciola hepatica, each by 45.3%, 45.9%, 57.9% and 50.8% respectively. Sequence analysis and alignment showed significant similarity to other eukaryotic cysteine proteinases, including the conservation of the cysteine, histidine, and asparagine residues that form the catalytic triad. A 1.5 kbp mRNA was detected on Northern blot analysis using full-length cysteine proteinase cDNA as a probe. The A. culbertsoni cysteine proteinase gene (AcCP2) was found to contain Ex3Rx3Wx2N at the proregion and also a proline/threonine-rich C-terminal extension. Therefore, it has cathepsin L-like characteristics. Phylogenetic analysis based on the amino acid sequences of cysteine proteinase indicated that AcCP2 was closely related with papaya, while it was remotely related with those of Schistosoma.

摘要

自由生活的变形虫,包括致病性的库氏棘阿米巴,广泛分布于土壤和淡水中。已发现半胱氨酸蛋白酶在致病性变形虫菌株中活性更高,而丝氨酸蛋白酶在致病性和非致病性菌株中均有发现。因此,半胱氨酸蛋白酶在几种寄生虫感染的发病机制中起重要作用,并已被提议作为基于结构的药物设计策略的靶点。作为将该策略应用于设计作为库氏棘阿米巴抗寄生虫剂的抑制剂的第一步,我们通过使用源自保守半胱氨酸蛋白酶序列的简并寡核苷酸引物进行逆转录-聚合酶链反应(RT-PCR),从库氏棘阿米巴中分离并测序了一个半胱氨酸蛋白酶基因的全长克隆。使用用于快速扩增cDNA末端(RACE)的PCR方案扩增半胱氨酸蛋白酶基因的5'和3'区域。它有一个1359 bp的开放阅读框。推导的氨基酸序列与卫氏并殖吸虫后尾蚴、曼氏血吸虫、人组织蛋白酶L和肝片吸虫的半胱氨酸蛋白酶基因的序列同源性分别为45.3%、45.9%、57.9%和50.8%。序列分析和比对显示与其他真核生物半胱氨酸蛋白酶有显著相似性,包括形成催化三联体的半胱氨酸、组氨酸和天冬酰胺残基的保守性。使用全长半胱氨酸蛋白酶cDNA作为探针进行Northern印迹分析时检测到一个1.5 kbp的mRNA。发现库氏棘阿米巴半胱氨酸蛋白酶基因(AcCP2)在前区含有Ex3Rx3Wx2N,并且在C末端还有一个富含脯氨酸/苏氨酸的延伸。因此,它具有组织蛋白酶L样特征。基于半胱氨酸蛋白酶氨基酸序列的系统发育分析表明,AcCP2与木瓜密切相关,而与血吸虫的关系较远。

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