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Z:一种具有钙依赖性亲和性的蛋白 A 衍生结构域,用于温和抗体纯化。

Z: A Protein A-Derived Domain with Calcium-Dependent Affinity for Mild Antibody Purification.

机构信息

Department of Protein Science, KTH Royal Institute of Technology, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), AlbaNova University Centre, Stockholm, Sweden.

出版信息

Methods Mol Biol. 2021;2178:245-249. doi: 10.1007/978-1-0716-0775-6_17.

Abstract

Therapeutic antibodies are at the forefront of modern medicine where high purity, which is typically obtained by Protein A-based affinity purification, is of utmost importance. In this chapter, we present a method for neutral and selective purification of antibodies by utilizing an engineered affinity ligand, Z, derived from Protein A. This domain displays a calcium-dependent binding of antibodies and has been multimerized and immobilized to a chromatography resin to achieve an affinity matrix with high binding capacity. IgG antibodies can be eluted from the tetrameric Z ligand at pH 7 with the addition of EDTA, or at pH 5.5 with EDTA for purification of monoclonal IgG1, which is significantly milder than the low pH (3-4) required in conventional Protein A affinity chromatography. Here, a protocol for selective capture of IgG with elution at neutral pH from a Z tetramer ligand immobilized on a chromatography resin is described.

摘要

治疗性抗体是现代医学的前沿领域,其中高纯度至关重要,通常通过基于蛋白 A 的亲和纯化来获得。在本章中,我们介绍了一种利用工程化的亲和配体 Z 来实现抗体的中性和选择性纯化的方法。该结构域表现出对抗体的钙离子依赖性结合,并已被多聚化并固定在色谱树脂上,以实现具有高结合容量的亲和基质。IgG 抗体可以在 pH 7 时加入 EDTA 从四聚体 Z 配体中洗脱,或者在 pH 5.5 时加入 EDTA 用于单克隆 IgG1 的纯化,这比传统的蛋白 A 亲和层析所需的低 pH(3-4)要温和得多。此处描述了一种从固定在色谱树脂上的 Z 四聚体配体中以中性 pH 洗脱 IgG 的选择性捕获方案。

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