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一种针对脂多糖中碳水化合物表位的单克隆抗体可将鹦鹉热嗜衣原体与猪嗜衣原体、肺炎嗜衣原体和沙眼衣原体区分开来。

A monoclonal antibody against a carbohydrate epitope in lipopolysaccharide differentiates Chlamydophila psittaci from Chlamydophila pecorum, Chlamydophila pneumoniae, and Chlamydia trachomatis.

作者信息

Müller-Loennies Sven, Gronow Sabine, Brade Lore, MacKenzie Roger, Kosma Paul, Brade Helmut

机构信息

Research Center Borstel, Leibniz Center for Medicine and Biosciences, Parkallee 22, D-23845 Borstel, Germany.

出版信息

Glycobiology. 2006 Mar;16(3):184-96. doi: 10.1093/glycob/cwj055. Epub 2005 Nov 10.

Abstract

Lipopolysaccharide (LPS) of Chlamydophila psittaci but not of Chlamydophila pneumoniae or Chlamydia trachomatis contains a tetrasaccharide of 3-deoxy-alpha-d-manno-oct-2-ulopyranosonic acid (Kdo) of the sequence Kdo(2-->8)[Kdo(2-->4)] Kdo(2-->4)Kdo. After immunization with the synthetic neoglycoconjugate antigen Kdo(2-->8)[Kdo(2-->4)]Kdo(2-->4) Kdo-BSA, we obtained the mouse monoclonal antibody (mAb) S69-4 which was able to differentiate C. psittaci from Chlamydophila pecorum, C. pneumoniae, and C. trachomatis in double labeling experiments of infected cell monolayers and by enzyme-linked immunosorbent assay (ELISA). The epitope specificity of mAb S69-4 was determined by binding and inhibition assays using bacteria, LPS, and natural or synthetic Kdo oligosaccharides as free ligands or conjugated to BSA. The mAb bound preferentially Kdo(2-->8)[Kdo(2-->4)]Kdo(2-->4)Kdo(2-->4) with a K(d) of 10 microM, as determined by surface plasmon resonance (SPR) for the monovalent interaction using mAb or single chain Fv. Cross-reactivity was observed with Kdo(2-->4)Kdo(2-->4) Kdo but not with Kdo(2-->8)Kdo(2-->4)Kdo, Kdo disaccharides in 2-->4- or 2-->8-linkage, or Kdo monosaccharide. MAb S69-4 was able to detect LPS on thin-layer chromatography (TLC) plates in amounts of <10 ng by immunostaining. Due to the high sensitivity achieved in this assay, the antibody also detected in vitro products of cloned Kdo transferases of Chlamydia. The antibody can therefore be used in medical and veterinarian diagnostics, general microbiology, analytical biochemistry, and studies of chlamydial LPS biosynthesis. Further contribution to the general understanding of carbohydrate-binding antibodies was obtained by a comparison of the primary structure of mAb S69-4 to that of mAb S45-18 of which the crystal structure in complex with its ligand has been elucidated recently (Nguyen et al., 2003, Nat. Struct. Biol., 10, 1019-1025).

摘要

鹦鹉热衣原体的脂多糖(LPS)含有序列为Kdo(2-->8)[Kdo(2-->4)] Kdo(2-->4)Kdo的3-脱氧-α-D-甘露糖-2-辛酮糖酸(Kdo)四糖,而肺炎衣原体或沙眼衣原体的脂多糖则不含。用合成的新糖缀合物抗原Kdo(2-->8)[Kdo(2-->4)]Kdo(2-->4) Kdo-BSA免疫后,我们获得了小鼠单克隆抗体(mAb)S69-4,在感染细胞单层的双重标记实验和酶联免疫吸附测定(ELISA)中,该抗体能够区分鹦鹉热衣原体与猪衣原体、肺炎衣原体和沙眼衣原体。mAb S69-4的表位特异性通过结合和抑制测定来确定,使用细菌、LPS以及天然或合成的Kdo寡糖作为游离配体或与BSA偶联。通过表面等离子体共振(SPR)测定单价相互作用(使用mAb或单链Fv),该mAb优先结合Kdo(2-->8)[Kdo(2-->4)]Kdo(2-->4)Kdo(2-->4),解离常数(K(d))为10 microM。观察到与Kdo(2-->4)Kdo(2-->4) Kdo有交叉反应,但与Kdo(2-->8)Kdo(2-->4)Kdo、2-->4-或2-->8-连接的Kdo二糖或Kdo单糖无交叉反应。mAb S69-4能够通过免疫染色在薄层色谱(TLC)板上检测到量小于10 ng的LPS。由于该测定法具有高灵敏度,该抗体还能检测衣原体克隆的Kdo转移酶的体外产物。因此,该抗体可用于医学和兽医诊断、普通微生物学、分析生物化学以及衣原体LPS生物合成研究。通过将mAb S69-4的一级结构与mAb S45-18的一级结构进行比较,对碳水化合物结合抗体的总体理解有了进一步贡献,mAb S45-18与其配体的复合物晶体结构最近已得到阐明(Nguyen等人,2003年,《自然结构生物学》,10,1019 - 1025)。

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