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PMID: 8714593 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Competition BIAcore for measuring true affinities: large differences from values determined from binding kinetics.

Analytical biochemistry ·Vol. 234 ·No. 2 ·1996-02-15 ·Pages 155-65

Nieba L, Krebber A, Plückthun A

Abstract

In attempting to use the BIAcore instrument for the determination of binding constants of several haptens or peptides to different antibodies by measuring on- and off-rates, we found that neither the absolute nor the relative values of the binding constants corresponded to the measurements in solution. Even at the lowest coupling densities useful for measurements, rebinding and bivalency effects offset the measurements by a factor of up to 500. We caution therefore about using on- and off-rates for the determination of absolute or even relative binding constants without controlling for rebinding and avidity effects. Instead, we show that binding constants in solution can be reproduced well by using on-rate determinations of antibody preincubated with antigen, and we derive the conditions under which such an approach is valid.

MeSH Terms
Antibody Affinity Binding, Competitive Biosensing Techniques Enzyme-Linked Immunosorbent Assay Epitope Mapping Haptens/immunology Kinetics Mathematics Molecular Structure Peptides/immunology Thermodynamics
Chemicals
Haptens Peptides
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nieba L
Biochemisches Institut der Universität Zürich, Switzerland.
Krebber A
Plückthun A
Article Info
Journal
Analytical biochemistry
Abbr.
Anal Biochem
ISSN
0003-2697
Published
1996-02-15
Pages
155-65
Language
English
Region
United States
NLM ID
0370535
Subset
IM
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