Journal
ANALYTICAL BIOCHEMISTRY
Volume 667, Issue -, Pages -Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ab.2023.115085
Keywords
Biosensor; Label -free; Kinetics; Affinity; SPR imaging
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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.
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