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使用SPOT肽阵列进行抗体表位图谱分析。

Antibody epitope mapping using SPOT peptide arrays.

作者信息

Reineke Ulrich, Sabat Robert

机构信息

Lead Discovery Biology Department, Jerini AG, Invalidenstr. 130, D-10115 Berlin, Germany.

出版信息

Methods Mol Biol. 2009;524:145-67. doi: 10.1007/978-1-59745-450-6_11.

Abstract

Information at the amino acid level about the epitopes of proteins recognized by antibodies or antibody fragments is important for their use as biological and diagnostic tools, therapeutic molecules, and for understanding molecular recognition events in general. The use of chemically prepared arrays of short peptides has emerged as a powerful tool to identify and characterize antibody epitopes. In this chapter the SPOT synthesis technique is described in detail. In addition, three different types of peptide libraries and their applications are described: protein sequence-derived scans of overlapping peptides (peptide scans) used to locate epitopes within the protein sequence, truncation libraries used to identify the minimal peptide length required for antibody binding, and complete substitutional analyses to identify the key residues important for antibody binding.

摘要

关于抗体或抗体片段所识别的蛋白质表位的氨基酸水平信息,对于将其用作生物学和诊断工具、治疗分子以及总体上理解分子识别事件而言非常重要。使用化学制备的短肽阵列已成为鉴定和表征抗体表位的有力工具。在本章中,将详细描述SPOT合成技术。此外,还将描述三种不同类型的肽文库及其应用:用于在蛋白质序列中定位表位的重叠肽的蛋白质序列衍生扫描(肽扫描)、用于鉴定抗体结合所需的最小肽长度的截短文库,以及用于鉴定对抗体结合重要的关键残基的完全取代分析。

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