Browse views: by Year, by Function, by GLF, by Subfunction, by Conference, by Journal

Determining the affinity and stoichiometry of interactions between unmodified proteins in solution using Biacore

Day, ES and Capili, AD and Borysenko, CW and Zafari, M and Whitty, A (2013) Determining the affinity and stoichiometry of interactions between unmodified proteins in solution using Biacore. Analytical Biochemistry. pp. 96-107.

Abstract

We describe a general Biacore method for measuring equilibrium binding affinities and stoichiometries for interactions between unmodified proteins and their unmodified ligands free in solution. Mixtures of protein and ligand are preequilibrated at different ratios in solution and then analyzed by Biacore using a sensor chip surface that detects only unbound analyte. Performing the Biacore analysis under mass transport limited conditions allows the concentration of unbound analyte to be determined from the initial velocity of binding. Plots of initial velocity versus the concentration of the varied binding partner are fitted to a quadratic binding equation to give the affinity and stoichiometry of binding. We demonstrate the method using soluble Her2 extracellular domain binding to monovalent, bivalent, and trivalent forms of an anti-Her2 antibody. The affinity we measured agrees with that obtained from conventional Biacore kinetic analysis, and the stoichiometries for the resulting 1:1, 1:2, and 1:3 complexes were confirmed by gel filtration with in-line light scattering. The method is applicable over an affinity range of approximately 100 pM to 1 muM and is particularly useful when there is concern that covalently modifying one or the other binding partner might affect its binding properties or where multivalency might otherwise complicate a quantitative analysis of binding. 2013 Elsevier Inc

Item Type: Article
Additional Information: pubid: 67 nvp_institute: NIBR contributor_address: (Day, Capili, Borysenko, Zafari) Biogen Idec, Cambridge, MA 02142, United States (Whitty) Department of Chemistry, Boston University, Boston, MA 02215, United States (Borysenko) Carnegie Melon University, Pittsburgh, PA 15213, United States (Zafari) Novartis Institutes for BioMedical Research, Cambridge, MA 02139, United States
Date Deposited: 13 Oct 2015 13:13
Last Modified: 13 Oct 2015 13:13
URI: https://oak.novartis.com/id/eprint/21910

Search

Email Alerts

Register with OAK to receive email alerts for saved searches.