1. Academic Validation
  2. Development of activity-based probes for cathepsin X

Development of activity-based probes for cathepsin X

  • ACS Chem Biol. 2011 Jun 17;6(6):563-72. doi: 10.1021/cb100392r.
Margot G Paulick 1 Matthew Bogyo
Affiliations

Affiliation

  • 1 Department of Pathology, Stanford University School of Medicine, 300 Pasteur Dr., Stanford, CA 94305-5324, United States.
Abstract

Cathepsin X is a lysosomal cysteine Protease that functions as a Carboxypeptidase with broad substrate specificity. Cathepsin X was discovered only recently, and its physiological roles are still not well understood. A number of studies suggest that Cathepsin X may be involved in a variety of biological processes, including Cancer, aging and degenerative conditions of the brain, inflammation, and cellular communication. Here we present the synthesis and characterization of several activity-based probes (ABPs) that target active Cathepsin X. These ABPs were used to label Cathepsin X in complex lysates, whole cells, and in vivo. Furthermore, we have developed a method for selectively labeling and visualizing active Cathepsin X in vitro and in vivo. Overall, the probes developed in this study are valuable tools for the study of Cathepsin X function.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-101779
    Cysteine Cathepsins Probe