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使用单克隆抗体鉴定和定位禾本科I组抗原上的变应原决定簇。

Identification and localization of allergenic determinants on grass group I antigens using monoclonal antibodies.

作者信息

Esch R E, Klapper D G

机构信息

Department of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill 27599.

出版信息

J Immunol. 1989 Jan 1;142(1):179-84.

PMID:2462587
Abstract

Epitopes recognized by five mAb which block the binding of human IgE antibodies to grass group I (GpI) Ag were characterized and partially mapped. Site specificity studies defined four apparently non-overlapping blocking antibody binding sites on the meadow fescue GpI molecule, Fes e I. One of these sites (site A) was localized to a 14,000 m.w. fragment designated P3 generated by CNBr cleavage of purified Fes e I. The P3 peptide possessed human IgE binding sites as well as other epitopes (non-site A) defined by 19 other anti-GpI mAb. All of the P3 reactive antibodies recognized cross-reactive determinants found on GpI Ag isolated from five different grasses suggesting that P3 is a conserved portion of grass GpI molecules. The P3 fragment from Fes e I was used to immunize mice and induced antibodies which reacted with intact GpI Ag from all 5 different grasses currently being studied in this laboratory.

摘要

对五种可阻断人IgE抗体与禾本科第I组(GpI)抗原结合的单克隆抗体(mAb)所识别的表位进行了特性鉴定和部分定位。位点特异性研究确定了草地羊茅GpI分子Fes e I上四个明显不重叠的阻断抗体结合位点。其中一个位点(位点A)定位于通过CNBr裂解纯化的Fes e I产生的一个14,000分子量的片段,称为P3。P3肽具有人IgE结合位点以及由其他19种抗GpI mAb定义的其他表位(非位点A)。所有与P3反应的抗体都识别从五种不同禾本科植物中分离出的GpI抗原上发现的交叉反应决定簇,这表明P3是禾本科GpI分子的保守部分。来自Fes e I的P3片段用于免疫小鼠,并诱导出与本实验室目前正在研究的所有5种不同禾本科植物的完整GpI抗原发生反应的抗体。

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