Mass spectrometry-based methods for characterizing transient protein–protein interactions

The dynamic associations of transient protein–protein interactions (PPIs) are critical mediators of myriad biochemical processes. These specific, low-affinity interactions are often mediated by conserved amino acid sequences or short linear motifs (SLiMs) that interact with corresponding binding domains. The short-lived and dynamic nature of these interactions make their biophysical characterization a significant challenge. This review focuses on the development and future directions of mass spectrometry (MS)-based techniques for elucidating and characterizing SLiM-mediated PPIs. This includes the application of protein footprinting techniques to infer the location of SLiM binding sites and the growing role of native MS for direct observation of protein–SLiM interactions, highlighting their potential for the assessment of small molecule modulation of transient PPIs and the identification of interfacial SLiMs.