Targeting the ATG5-ATG16L1 Protein-Protein Interaction with a Hydrocarbon-Stapled Peptide Derived from ATG16L1 for Autophagy Inhibition

Selective modulation of autophagy is a promising therapeutic strategy, especially for cancer treatment. However, the lack of specific autophagy inhibitors limits this strategy. The formation of the ATG12???ATG5???ATG16L1 complex is essential for targeting the ATG12???ATG5 conjugate to proper membranes and to generate LC3-II for the progression of autophagy. Thus, targeting ATG5???ATG16L1 protein???protein interactions (PPIs) might inhibit early stage autophagy with high specificity. In this paper, we report that a stapled peptide derived from ATG16L1 exhibits potent binding affinity to ATG5, striking resistance to proteolysis, and significant autophagy inhibition activities in cells. Superscript/Subscript Available

Automated summary

The study demonstrates that a stapled peptide derived from ATG16L1 exhibits potent binding affinity to ATG5, strong resistance to proteolysis, and significant autophagy inhibition activities in cells.