Active-Site-Directed Chemical Tools for Profiling Mitochondrial Lon Protease

• Published in: ACS chemical biology 2011-08, Vol.6 (8), p.781-788
• Main Authors: Fishovitz, Jennifer, Li, Min, Frase, Hilary, Hudak, Jason, Craig, Sandra, Ko, Kristin, Berdis, Anthony J, Suzuki, Carolyn K, Lee, Irene
• Format: Article
• Language: English
• Subjects: Adenosine Triphosphate - metabolism; Catalytic Domain; Endopeptidase Clp - antagonists & inhibitors; Endopeptidase Clp - metabolism; Enzyme Inhibitors - analysis; Enzyme Inhibitors - metabolism; Fluorescent Dyes - analysis; Fluorescent Dyes - metabolism; HeLa Cells; Humans; Mitochondria - metabolism; Mitochondrial Proteins - antagonists & inhibitors; Mitochondrial Proteins - metabolism; Peptides - analysis; Peptides - metabolism; Protease La - antagonists & inhibitors; Protease La - metabolism; Proteolysis
• ISSN: 1554-8929; 1554-8937
• DOI: 10.1021/cb100408w

Lon and ClpXP are the only soluble ATP-dependent proteases within the mammalian mitochondria matrix, which function in protein quality control by selectively degrading misfolded, misassembled, or damaged proteins. Chemical tools to study these proteases in biological samples have not been identified, thereby hindering a clear understanding of their respective functions in normal and disease states. In this study, we applied a proteolytic site-directed approach to identify a peptide reporter substrate and a peptide inhibitor that are selective for Lon but not ClpXP. These chemical tools permit quantitative measurements that distinguish Lon-mediated proteolysis from that of ClpXP in biochemical assays with purified proteases, as well as in intact mitochondria and mitochondrial lysates. This chemical biology approach provides needed tools to further our understanding of mitochondrial ATP-dependent proteolysis and contributes to the future development of diagnostic and pharmacological agents for treating diseases associated with defects in mitochondrial protein quality.