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Updated: Sep 16, 2026

Proofreading and DNA Repair Assay Using Single Nucleotide Extension and MALDI-TOF Mass Spectrometry Analysis
Published on: June 19, 2018
Rapid assay optimization by plug-and-play MAPPIT
Stefanie Maes1,2, Louis Delhaye1,2, Robin Cooreman1,3
1VIB-UGent Center for Medical Biotechnology, VIB, Ghent, Belgium.
Abstract:
Studying protein-protein interactions, which are crucial for all cellular processes in both health and disease, offers valuable insights into underlying mechanisms and reveals promising therapeutic targets. While efforts have been made to vastly increase the scale of MAPPIT assays, covering the full protein interactome remains challenging, in particular when considering the availability of different assay configurations. In this study, we expanded our Golden Gate modular cloning platform to enable rapid, customizable construct assembly for MAPPIT assays. We demonstrate the strength of this expanded toolbox for multiple distinct protein-protein interactions, including a MAPPIT assay for six different intracellular VHHs targeting the antiviral effector protein MXA.

