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首页> 外文期刊>Journal of Immunological Methods >On-bead antibody-small molecule conjugation using high-capacity magnetic beads
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On-bead antibody-small molecule conjugation using high-capacity magnetic beads

机译:使用高容量磁珠的珠上抗体-小分子偶联

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Antibodies labeled with small molecules such as fluorophore, biotin or drugs play an important role in various areas of biological research, drug discovery and diagnostics. However, the majority of current methods for labeling antibodies is solution-based and has several limitations including the need for purified antibodies at high concentrations and multiple buffer exchange steps. In this study, a method (on-bead conjugation) is described that addresses these limitations by combining antibody purification and conjugation in a single workflow. This method uses high capacity-magnetic Protein A or Protein G beads to capture antibodies directly from cell media followed by conjugation with small molecules and elution of conjugated antibodies from the beads. High-capacity magnetic antibody capture beads are key to this method and were developed by combining porous and hydrophilic cellulose beads with oriented immobilization of Protein A and Protein G using HaloTag technology. With a variety of fluorophores it is shown that the on-bead conjugation method is compatible with both thiol- and amine-based chemistry. This method enables simple and rapid processing of multiple samples in parallel with high-efficiency antibody recovery. It is further shown that recovered antibodies are functional and compatible with downstream applications. (C) 2015 The Authors. Published by Elsevier B.V.
机译:用小分子标记的抗体,例如荧光团,生物素或药物,在生物学研究,药物发现和诊断的各个领域中发挥着重要作用。但是,目前用于标记抗体的大多数方法都是基于溶液的方法,并且存在一些局限性,包括需要高浓度的纯化抗体和多个缓冲液交换步骤。在这项研究中,描述了一种方法(珠上结合),该方法通过在单个工作流程中结合抗体纯化和结合来解决这些限制。该方法使用高容量的磁性蛋白A或蛋白G磁珠直接从细胞培养基中捕获抗体,然后与小分子结合并从磁珠中洗脱结合的抗体。高容量磁性抗体捕获珠是该方法的关键,并通过使用HaloTag技术将多孔和亲水性纤维素珠与定向固定化的A蛋白和G蛋白结合而开发。对于多种荧光团,显示珠上偶联方法与基于硫醇和胺的化学方法均兼容。这种方法可以简单,快速地处理多个样品,并实现高效抗体回收。进一步显示回收的抗体是功能性的并且与下游应用兼容。 (C)2015作者。由Elsevier B.V.发布

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