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The Role of ClpP Protease in Bacterial Pathogenesis and Human Diseases.
- Source :
-
ACS chemical biology [ACS Chem Biol] 2018 Jun 15; Vol. 13 (6), pp. 1413-1425. Date of Electronic Publication: 2018 Jun 01. - Publication Year :
- 2018
-
Abstract
- In prokaryotic cells and eukaryotic organelles, the ClpP protease plays an important role in proteostasis. The disruption of the ClpP function has been shown to influence the infectivity and virulence of a number of bacterial pathogens. More recently, ClpP has been found to be involved in various forms of carcinomas and in Perrault syndrome, which is an inherited condition characterized by hearing loss in males and females and by ovarian abnormalities in females. Hence, targeting ClpP is a potentially viable, attractive option for the treatment of different ailments. Herein, the biochemical and cellular activities of ClpP are discussed along with the mechanisms by which ClpP affects bacterial pathogenesis and various human diseases. In addition, a comprehensive overview is given of the new classes of compounds in development that target ClpP. Many of these compounds are currently primarily aimed at treating bacterial infections. Some of these compounds inhibit ClpP activity, while others activate the protease and lead to its dysregulation. The ClpP activators are remarkable examples of small molecules that inhibit protein-protein interactions but also result in a gain of function.
- Subjects :
- Adenosine Triphosphatases antagonists & inhibitors
Anti-Bacterial Agents pharmacology
Bacteria drug effects
Bacterial Infections drug therapy
Bacterial Proteins antagonists & inhibitors
Endopeptidase Clp antagonists & inhibitors
Endopeptidase Clp chemistry
Enzyme Inhibitors pharmacology
Heat-Shock Proteins antagonists & inhibitors
Humans
Mitochondria physiology
Mycobacterium tuberculosis drug effects
Mycobacterium tuberculosis enzymology
Bacterial Infections physiopathology
Endopeptidase Clp physiology
Neoplasms physiopathology
Subjects
Details
- Language :
- English
- ISSN :
- 1554-8937
- Volume :
- 13
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- ACS chemical biology
- Publication Type :
- Academic Journal
- Accession number :
- 29775273
- Full Text :
- https://doi.org/10.1021/acschembio.8b00124