PACTS-Assisted Thermal Proteome Profiling for Use in Identifying Peptide-Interacting Proteins

Bioactive peptides play important roles in various biological processes. However, the traditional methods for profiling the peptide-interacting proteins require modifications to the peptide molecules, often leading to false identifications. We found that the interaction between peptide ligands and protein receptors induced significant changes in the abundance of the interacting proteins, which is a signature indicating the interaction and providing complementary information for use in the classical thermal proteome profiling (TPP) technique. Herein, we developed a novel Peptide-ligand-induced Abundance Change of proTeinS (PACTS)-assisted TPP strategy for the identification of peptide-interacting proteins based on the peptide-ligand-induced change in protein abundance. The utility and efficacy of this approach were demonstrated by the identification of the interaction of the protein 3-phosphoinositide-dependent protein kinase 1 (PDPK1) and PDPK1-interacting fragment (PIF) pair and by large-scale profiling of the interacting proteins of PIF. The PACTS-assisted TPP approach was applied to describe the interactome of amyloid beta (A beta) 1-42 in THP-1 cells and resulted in the identification of 103 interacting proteins. Validation experiments indicated that A beta 1-42 interacted directly with fatty acid synthase and inhibited its enzymatic activity, providing insights into fatty acid metabolic disorders in Alzheimer's disease (AD). Overall, PACTS-assisted TPP is an efficient approach, and the newly identified A beta-interacting proteins provide rich resources for the research on AD.

Automated summary

The Peptide-ligand-induced Abundance Change of proTeinS (PACTS)-assisted TPP strategy is an efficient approach for the identification of peptide-interacting proteins. Using this method, we successfully identified the interaction of 3-phosphoinositide-dependent protein kinase 1 (PDPK1) and PDPK1-interacting fragment (PIF) pair, as well as the interaction proteins of Aβ1-42 in THP-1 cells.