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Updated: May 2, 2026

Author Spotlight: Optimizing Affinity Chromatography for His-Tagged FEN1 Protein
Published on: April 26, 2024
Measuring binding constants of His-tagged proteins using affinity chromatography and Ni-NTA-immobilized enzymes
Annette C Moser1, Benjamin White, Frank A Kovacs
1Chemistry Department, University of Nebraska at Kearney, 905 West 25th Street, Kearney, NE, 68849-1150, USA, moserac@unk.edu.
Abstract:
Affinity chromatography is one way to measure the binding constants of a protein-ligand interaction. Here we describe a method of measuring a binding constant using Ni-NTA resin to immobilize a His-tagged enzyme and the method of frontal analysis. While other methods of immobilization are possible, using the strong affinity interaction between His-tagged proteins and Ni-NTA supports results in a fast, easy, and gentle method of immobilization. Once the affinity support is created, frontal analysis can be used to measure the binding constant between the protein and various analytes.

