Biopanning for the characterization of allergen mimotopes.

Isabella Pali-Schöll, Erika Jensen-Jarolim
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引用次数: 6

Abstract

Proper understanding of the pathogenesis of type I allergy relies on the identification of allergen epitopes. The phage display technique is a relatively new one to define peptide structures that mimic natural epitopes, including conformational B-cell epitopes. Peptides displayed on the phage recognized by an antiallergen antibody mimic the physicochemical properties of the amino acids and are, therefore, called mimotopes. The main advantage of the biopanning technique described in this chapter is that the structure of the antigen/allergen may be completely unknown; the only material needed is an antibody binding to it. The mimotopes generated by this technique display the features of the antigen/allergen but do not crosslink the mast cell-bound IgE-antibodies. Thus mimotopes could be used as a safe alternative to the commonly applied allergen extracts in immunotherapy of allergic patients and direct the immune response toward the desired allergen epitopes. In the selection procedure called biopanning, phages with the mimotopes best recognized by the selecting antibody are amplified. The titers of phages specifically binding to the selection antibody are checked. In this chapter we describe two alternative methods for colony screening: the immunoblot and ELISA.

变态反应原模位特征的生物筛选。
正确理解I型过敏的发病机制依赖于过敏原表位的鉴定。噬菌体展示技术是一种相对较新的技术,用于定义模仿天然表位的肽结构,包括构象b细胞表位。被抗过敏原抗体识别的噬菌体上显示的肽模仿氨基酸的物理化学性质,因此被称为模位。本章描述的生物筛选技术的主要优点是抗原/过敏原的结构可能是完全未知的;唯一需要的材料是与它结合的抗体。该技术产生的模位显示抗原/过敏原的特征,但不与肥大细胞结合的ige抗体交联。因此,mimotopes可以作为过敏原提取物的安全替代品,用于过敏患者的免疫治疗,并将免疫反应导向所需的过敏原表位。在被称为生物筛选的选择过程中,具有最能被选择抗体识别的同种异体的噬菌体被扩增。检测与选择抗体特异性结合的噬菌体滴度。在本章中,我们描述了菌落筛选的两种替代方法:免疫印迹和ELISA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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