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用于交叉反应性测定的肽微阵列。

Peptide microarrays for determination of cross-reactivity.

作者信息

Thiele Alexandra

机构信息

Max Planck Research Unit for Enzymology of Protein Folding, Weinbergweg 22, 06120 Halle, Germany.

出版信息

Methods Mol Biol. 2009;524:225-34. doi: 10.1007/978-1-59745-450-6_16.

Abstract

Polyclonal antibodies raised against full-length antigens are often used for localization experiments. Exact knowledge of epitopes in the antigen recognized by the antiserum is important if the target antigen belongs to a large family of proteins which are highly conserved. We have shown that epitope mapping using peptide microarrays represents a powerful tool for determination of immunodominat regions in a proteome-wide manner. As examples we show results of epitope mapping using peptide microarrays displaying overlapping peptide scans through either all human cyclophilins or all human FK506-binding proteins.

摘要

针对全长抗原产生的多克隆抗体常用于定位实验。如果靶抗原属于高度保守的蛋白质大家族,那么准确了解抗血清所识别抗原中的表位就很重要。我们已经表明,使用肽微阵列进行表位作图是一种以蛋白质组范围方式确定免疫显性区域的强大工具。作为示例,我们展示了使用肽微阵列进行表位作图的结果,这些肽微阵列展示了通过所有人类亲环蛋白或所有人类FK506结合蛋白的重叠肽扫描。

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