4.5 Article

Gradient method for accurate affinity determinations

期刊

ANALYTICAL BIOCHEMISTRY
卷 667, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ab.2023.115085

关键词

Biosensor; Label -free; Kinetics; Affinity; SPR imaging

向作者/读者索取更多资源

This paper presents a new SPR-imaging method that uses a ligand density gradient to extrapolate analyte response. This method avoids cumbersome optimization procedures and minimizes surface dependent effects. The method can be fully automated for accurate determination of antibody quality from commercial sources.
The value of the affinity constants (kd, ka, and KD) that are determined by label free interaction analysis methods are strongly affected by the ligand density at the sensor surface [1]. This paper outlines a new SPR-imaging method that applies a ligand density gradient enabling the analyte response to be extrapolated to Rmax = 0 mu RIU. The mass transport limited region is used to determine the analyte concentration. Cumbersome opti-mization procedures for tuning the ligand density is prevented and surface dependent effects as rebinding, strong biphasic behavior etcetera are minimized. The method can be fully automated for e.g. accurate determination of the quality of antibodies from commercial sources.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据