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通过噬菌体展示扣除法从头鉴定细胞类型特异性抗体-抗原对。分离出一种抗人角蛋白14的人单链抗体片段。

De novo identification of cell-type specific antibody-antigen pairs by phage display subtraction. Isolation of a human single chain antibody fragment against human keratin 14.

作者信息

Stausbøl-Grøn B, Jensen K B, Jensen K H, Jensen M Ø, Clark B F

机构信息

Department of Dermatology, Marselisborg Hospital, University of Aarhus, Denmark.

出版信息

Eur J Biochem. 2001 May;268(10):3099-107. doi: 10.1046/j.1432-1327.2001.02210.x.

Abstract

The aim of this study was to identify novel antibodies directed against cytosolic keratinocyte-specific antigens from a phage display antibody repertoire by using phage display subtraction. Phage display is a method of displaying foreign molecules on the surface of filamentous bacteriophage particles. It allows the interaction between two cognate molecules to be analysed through affinity selections. Recently, large repertoires of phage displayed human antibody fragments have been constructed. From such repertoires, antibodies can be obtained in vitro without the need for immunization or the hybridoma technology. A novel subtractive strategy for selecting antibodies from phage libraries was applied. Phage antibodies were selected against immobilized crude lysates of cultured human keratinocytes, the target antigens being unknown beforehand. A competing cell lysate was used to reduce retrieval of phage antibodies with specificities to commonly non-differentially expressed antigens. A monoclonal single chain fragment variable (scFv) with specificity for crude lysates of cultured human keratinocytes was identified as demonstrated by ELISA assays and immunoblotting analysis. The cognate keratinocyte antigen was shown to be keratin 14 (K14) by using immunoblotting based on 2D PAGE and a corresponding 2D PAGE protein database. In accordance with the expected tissue localization of K14, the identified scFv stained the basal layer of human epidermis by indirect immunofluorescence analysis. Starting with crude cell lysates, phage display subtraction in combination with 2D PAGE and 2D PAGE protein databases can be used to identify antibody-antigen pairs that characterize a specific cell type.

摘要

本研究的目的是通过噬菌体展示消减技术,从噬菌体展示抗体库中鉴定针对细胞溶质角质形成细胞特异性抗原的新型抗体。噬菌体展示是一种在丝状噬菌体颗粒表面展示外源分子的方法。它允许通过亲和选择分析两个同源分子之间的相互作用。最近,已经构建了大量噬菌体展示的人抗体片段库。利用这些文库,可以在体外获得抗体,而无需免疫或杂交瘤技术。应用了一种从噬菌体文库中选择抗体的新型消减策略。针对固定化的培养人角质形成细胞粗裂解物选择噬菌体抗体,靶抗原事先未知。使用竞争性细胞裂解物减少对通常非差异表达抗原具有特异性的噬菌体抗体的回收。通过ELISA分析和免疫印迹分析证明,鉴定出一种对培养人角质形成细胞粗裂解物具有特异性的单克隆单链可变片段(scFv)。通过基于二维聚丙烯酰胺凝胶电泳(2D PAGE)和相应的二维聚丙烯酰胺凝胶电泳蛋白质数据库的免疫印迹分析,同源角质形成细胞抗原显示为角蛋白14(K14)。根据K14预期的组织定位,通过间接免疫荧光分析,鉴定出的scFv对人表皮基底层进行了染色。从粗细胞裂解物开始,噬菌体展示消减技术与二维聚丙烯酰胺凝胶电泳和二维聚丙烯酰胺凝胶电泳蛋白质数据库相结合,可用于鉴定表征特定细胞类型的抗体-抗原对。

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