Abstract

Proteases are involved in the control of numerous physiological processes, and their dysregulation has been identified in a wide range of pathologies, including cancer. Protease activity is normally tightly regulated post-translationally and therefore cannot be accurately estimated based on mRNA or protein expression alone. While several types of zymography approaches to estimate protease activity exist, there remains a need for a robust and reliable technique to measure protease activity in biological tissues. We present a novel quantitative ex vivo zymography (QZ) technology based on Probody® therapeutics (Pb-Tx), a novel class of protease-activated cancer therapeutics that contain a substrate linker cleavable by tumor-associated proteases. This approach enables the measurement and comparison of protease activity in biological tissues via the detection of Pb-Tx activation. By exploiting substrate specificity and selectivity, cataloguing and differentiating protease activities is possible, with further refinement achieved using protease-specific inhibitors. Using the QZ assay and human tumor xenografts, patient tumor tissues, and patient plasma, we characterized protease activity in preclinical and clinical samples. The QZ assay offers the potential to increase our understanding of protease activity in tissues and inform diagnostic and therapeutic development for diseases, such as cancer, that are characterized by dysregulated proteolysis.

Highlights

  • Proteases, or proteolytic enzymes, catalyze the breakdown of proteins by hydrolysis of peptide bonds

  • Western capillary electrophoresis (Wes) previously reported an IHZ technology based on the unique features of a Pb-Tx and IHC, which can be applied to profile and monitor protease activity in any biological tissue [43]

  • We present an improved version of the assay, which is based on Pb-Tx technology and capillary electrophoresis and does not require target binding for protease activity assessment

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Summary

Introduction

Proteolytic enzymes, catalyze the breakdown of proteins by hydrolysis of peptide bonds. Protease activity is tightly regulated through multiple redundant mechanisms, including gene expression, zymogen activation, endogenous inhibitors, subcellular localization, and post-translational modifications [3]. Protease dysregulation has been identified in a wide range of pathologies, including cardiovascular, neurodegenerative and inflammatory diseases, infection, and cancer [2]. Dysregulated proteolysis is central to carcinogenesis by playing key roles in tumor progression-associated processes, including growth, invasion, and metastasis [9,10,11]. Due to their involvement in multiple pathologies, proteases represent attractive biomarkers or drug targets in wide-ranging therapeutic areas, including cancer

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