Dan Loewenthal

This paper introduces a method for continuous mass photometry of single molecules, enabling long-term observation of biomolecular interactions with high mass precision and temporal resolution.

This study investigates how ligand binding dynamically influences QR2 dimerization and function using native mass spectrometry.

This study directly observes and quantifies the self-assembly of virus-like particles using mass photometry and single-molecule trapping, revealing the role of multivalent interactions and first-passage dynamics in achieving specific assembly.

This paper provides guidelines for optimizing mass photometry to achieve high mass resolution and detection limits while maintaining simplicity.