表面等离子体共振成像检测细胞抗体亲和度的新方法。

IF 5.6 3区 工程技术 Q1 CHEMISTRY, ANALYTICAL
Richard B M Schasfoort, Elise van Doorn, Jos van Weperen, Anouk Mentink, Ruchi Bansal
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引用次数: 0

摘要

近年来,亲和度已成为抗体设计的一个关键参数,但目前大多数分析仪器仅限于单独测量亲和度。本研究旨在评估一种新型表面等离子体共振成像仪器CellVysion的能力和优势,该仪器设计用于使用连续抗体密度梯度来量化细胞抗体的亲和度。这种方法的一个关键特征是确定一个“临界点”——特定的配体密度,以µRIUs为单位测量,在这个临界点上,细胞在定义的剪切流条件下仍然与传感器表面结合。在本文中,我们介绍了该方法的技术原理和应用,展示了如何在不同的抗体-细胞系组合中定量评估亲和度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A New Approach to Examine Cell-Antibody Avidity with Surface Plasmon Resonance Imaging.

A New Approach to Examine Cell-Antibody Avidity with Surface Plasmon Resonance Imaging.

A New Approach to Examine Cell-Antibody Avidity with Surface Plasmon Resonance Imaging.

A New Approach to Examine Cell-Antibody Avidity with Surface Plasmon Resonance Imaging.

In recent years, avidity has emerged as a critical parameter in antibody design, yet most current analytical instruments are limited to measuring affinity alone. This study aims to evaluate the capabilities and advantages of a novel surface plasmon resonance imaging instrument, CellVysion, designed to quantify cell-antibody avidity using a continuous antibody density gradient. A key feature of this approach is the identification of a "tipping point"-the specific ligand density, measured in µRIUs, at which cells remain bound to the sensor surface under defined shear flow conditions. In this paper, we present the technical principles and application of this method, demonstrating how avidity can be quantitatively assessed across different antibody-cell line combinations.

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来源期刊
Biosensors-Basel
Biosensors-Basel Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
6.60
自引率
14.80%
发文量
983
审稿时长
11 weeks
期刊介绍: Biosensors (ISSN 2079-6374) provides an advanced forum for studies related to the science and technology of biosensors and biosensing. It publishes original research papers, comprehensive reviews and communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files and software regarding the full details of the calculation or experimental procedure, if unable to be published in a normal way, can be deposited as supplementary electronic material.
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