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对侵蚀艾肯菌粘附素复合体中一个接近碳水化合物识别结构域的蛋白质成分的编码基因进行分子分析。

Molecular analysis of the gene encoding a protein component of the Eikenella corrodens adhesin complex that is close to the carbohydrate recognition domain.

作者信息

Azakami H, Yumoto H, Nakae H, Matsuo T, Ebisu S

机构信息

Department of Conservative Dentistry, Tokushima University School of Dentistry, Japan.

出版信息

Gene. 1996 Nov 21;180(1-2):207-12. doi: 10.1016/s0378-1119(96)00639-7.

Abstract

A monoclonal antibody against a lectin-like substance (LS) of Eikenella corrodens (Ec) was used for screening the Ec DNA library. Three positive clones that carried an identical 12-kb segment were obtained. A 25-kDa protein, which specifically binds to the antibody, was overproduced in all of the Escherichia coli clones. Deletion analysis showed that the gene encoding the 25-kDa protein was located within a 1.2-kb segment. The nucleotide (nt) sequence of this segment contained an open reading frame encoding a protein of 24600 Da. We purified the 25-kDa protein from the cloned E. coli strain. The sequence of the first 10 amino acids(aa) from the N-terminus of the purified 25-kDa protein agreed with that deduced from the nt sequence. Since the monoclonal antibody used in this study inhibits the physiological activity of EcLS, we concluded that the 25-kDa protein is a component of the adhesin complex, which is located near the carbohydrate recognition domain of lectin in EcLS.

摘要

一种针对腐蚀艾肯菌(Ec)凝集素样物质(LS)的单克隆抗体被用于筛选Ec DNA文库。获得了三个携带相同12 kb片段的阳性克隆。在所有大肠杆菌克隆中均过量产生了一种与该抗体特异性结合的25 kDa蛋白。缺失分析表明,编码25 kDa蛋白的基因位于一个1.2 kb的片段内。该片段的核苷酸(nt)序列包含一个编码24600 Da蛋白的开放阅读框。我们从克隆的大肠杆菌菌株中纯化了25 kDa蛋白。纯化的25 kDa蛋白N端前10个氨基酸(aa)的序列与从nt序列推导的序列一致。由于本研究中使用的单克隆抗体抑制EcLS的生理活性,我们得出结论,25 kDa蛋白是粘附素复合物的一个组成部分,位于EcLS中凝集素的碳水化合物识别结构域附近。

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