Sensitive ELISA-based detection method for the mitophagy marker p-S65-Ub in human cells, autopsy brain, and blood samples
| Autor: | Xu Hou, Fabienne C. Fiesel, Jens O. Watzlawik, Michael G. Heckman, Wolfdieter Springer, Owen A. Ross, Matthew S. Goldberg, Zbigniew K. Wszolek, Michael DeTure, Sandeep Kumar Barodia, Dennis W. Dickson, Joanna Siuda, Chloe Ramnarine, Tania F. Gendron, Guojun Bu, Dominika Fricova, Clemens R. Scherzer |
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| Jazyk: | angličtina |
| Rok vydání: | 2020 |
| Předmět: |
0301 basic medicine
autophagy Ubiquitin-Protein Ligases Autopsy PINK1 Enzyme-Linked Immunosorbent Assay Disease Parkin 03 medical and health sciences Mice Ubiquitin Mitophagy medicine Animals Humans PRKN Molecular Biology 030102 biochemistry & molecular biology biology Autophagy Brain Cell Biology medicine.disease nervous system diseases Parkinson disease 030104 developmental biology Cancer research biology.protein Alzheimer's disease Alzheimer disease Toolbox Protein Kinases Research Article |
| Zdroj: | Autophagy article-version (VoR) Version of Record |
| ISSN: | 1554-8635 1554-8627 |
| Popis: | Mitochondrial dysfunction is an early, imminent event in neurodegenerative disorders including Parkinson disease (PD) and Alzheimer disease (AD). The enzymatic pair PINK1 and PRKN/Parkin recognize and transiently label damaged mitochondria with ubiquitin (Ub) phosphorylated at Ser65 (p-S65-Ub) as a signal for degradation via the autophagy-lysosome system (mitophagy). Despite its discovery in cell culture several years ago, robust and quantitative detection of altered mitophagy in vivo has remained challenging. Here we developed a sandwich ELISA targeting p-S65-Ub with the goal to assess mitophagy levels in mouse brain and in human clinical and pathological samples. We characterized five total Ub and four p-S65-Ub antibodies by several techniques and found significant differences in their ability to recognize phosphorylated Ub. The most sensitive antibody pair detected recombinant p-S65-Ub chains in the femtomolar to low picomolar range depending on the poly-Ub chain linkage. Importantly, this ELISA was able to assess very low baseline mitophagy levels in unstressed human cells and in brains from wild-type and prkn knockout mice as well as elevated p-S65-Ub levels in autopsied frontal cortex from AD patients vs. control cases. Moreover, the assay allowed detection of p-S65-Ub in blood plasma and was able to discriminate between PINK1 mutation carriers and controls. In summary, we developed a robust and sensitive tool to measure mitophagy levels in cells, tissue, and body fluids. Our data strongly support the idea that the stress-activated PINK1-PRKN mitophagy pathway is constitutively active in mice and humans under unstimulated, physiological and elevated in diseased, pathological conditions. Abbreviations: Ab: antibody; AD: Alzheimer disease; AP: alkaline phosphatase; CV: coefficient of variation; ECL: electrochemiluminescence; KO: knockout; LoB: Limit of Blank; LoD: Limit of Detection; LoQ: Limit of Quantification; MSD: meso scale discovery; PD: Parkinson disease; p-S65-PRKN: phosphorylated PRKN at serine 65; p-S65-Ub: phosphorylated ubiquitin at serine 65; Std.Dev.: standard deviation; Ub: ubiquitin; WT: wild type |
| Databáze: | OpenAIRE |
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