Protease Activity Profiling via Programmable Phage Display of Comprehensive Proteome-Scale Peptide Libraries

Cell Syst. 2020 Oct 21;11(4):375-381.e4. doi: 10.1016/j.cels.2020.08.013. Epub 2020 Sep 23.

Abstract

Endopeptidases catalyze the internal cleavage of proteins, playing pivotal roles in protein turnover, substrate maturation, and the activation of signaling cascades. A broad range of biological functions in health and disease are controlled by proteases, yet assays to characterize their activities at a proteomic scale do not exist. To address this unmet need, we developed Sensing EndoPeptidase Activity via Release and recapture using flAnking Tag Epitopes (SEPARATE), which uses a monovalent phage display of the human proteome at a 90-aa peptide resolution. We demonstrate that SEPARATE is compatible with several human proteases from distinct catalytic classes, including caspase-1, ADAM17, and thrombin. Both well-characterized and newly identified substrates of these enzymes were detected in the assay. SEPARATE was used to discover a non-canonical caspase-1 substrate, the E3 ubiquitin ligase HUWE1, a key mediator of apoptotic cell death. SEPARATE enables efficient, unbiased assessment of endopeptidase activity by using a phage-displayed proteome. A record of this paper's Transparent Peer Review process is included in the Supplemental Information.

Keywords: next generation DNA sequencing; programmable phage display; protease activity profiling; proteomic analysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM17 Protein / metabolism
  • Caspase 1 / metabolism
  • Cell Surface Display Techniques / methods*
  • Humans
  • Peptide Hydrolases / metabolism*
  • Peptide Library
  • Peptides / analysis*
  • Peptides / chemistry
  • Proteolysis
  • Proteome / metabolism
  • Proteomics / methods*
  • Substrate Specificity
  • THP-1 Cells
  • Thrombin / metabolism
  • Tumor Suppressor Proteins / metabolism
  • Ubiquitin-Protein Ligases / metabolism

Substances

  • Peptide Library
  • Peptides
  • Proteome
  • Tumor Suppressor Proteins
  • Ubiquitin-Protein Ligases
  • Peptide Hydrolases
  • Thrombin
  • Caspase 1
  • ADAM17 Protein