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Activity-Based Probes for the High Temperature Requirement A Serine Proteases
- Source :
- ACS Chemical Biology. 15:2346-2354
- Publication Year :
- 2020
- Publisher :
- American Chemical Society (ACS), 2020.
-
Abstract
- The high temperature requirement A (HTRA) family of serine proteases mediates protein quality control. These proteins process misfolded proteins in several diseases including Alzheimer's disease (AD) and Parkinson's disease (PD). While their structures and activation mechanisms have been studied, the precise details of the regulation of their activity under physiological conditions have not been completely elucidated, partly due to the lack of suitable chemical probes. In the present study, we developed novel activity-based probes (ABPs) targeting the HTRAs and demonstrated their utility in the monitoring and quantification of changes in enzyme activity in live cells. Using our probes, we found the activity of HTRA1 to be highly elevated in an AD-like cell-based model. We also observed the active HTRA2 in live cells by using a mitochondrion-targeted probe. We believe that our probes can serve as a useful tool to study the role of human HTRAs in neurodegenerative diseases.
- Subjects :
- 0301 basic medicine
Proteases
Cell
Organophosphonates
01 natural sciences
Biochemistry
Serine
03 medical and health sciences
Cell Line, Tumor
medicine
Humans
Fluorescent Dyes
Microscopy, Confocal
biology
010405 organic chemistry
Chemistry
High-Temperature Requirement A Serine Peptidase 1
General Medicine
High-Temperature Requirement A Serine Peptidase 2
Fluoresceins
Enzyme assay
Mitochondria
0104 chemical sciences
030104 developmental biology
medicine.anatomical_structure
Microscopy, Fluorescence
Cell culture
Molecular Probes
HTRA1
biology.protein
Molecular Medicine
Protein folding
Oligopeptides
Protein quality
Subjects
Details
- ISSN :
- 15548937 and 15548929
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- ACS Chemical Biology
- Accession number :
- edsair.doi.dedup.....413a5077009a8a499fe96be95526d102
- Full Text :
- https://doi.org/10.1021/acschembio.0c00279