A Multiplexed High-Content Screening Approach Using the Chromobody Technology to Identify Cell Cycle Modulators in Living Cells. (October 2016)
- Record Type:
- Journal Article
- Title:
- A Multiplexed High-Content Screening Approach Using the Chromobody Technology to Identify Cell Cycle Modulators in Living Cells. (October 2016)
- Main Title:
- A Multiplexed High-Content Screening Approach Using the Chromobody Technology to Identify Cell Cycle Modulators in Living Cells
- Authors:
- Schorpp, Kenji
Rothenaigner, Ina
Maier, Julia
Traenkle, Bjoern
Rothbauer, Ulrich
Hadian, Kamyar - Abstract:
- Many screening hits show relatively poor quality regarding later efficacy and safety. Therefore, small-molecule screening efforts shift toward high-content analysis providing more detailed information. Here, we describe a novel screening approach to identify cell cycle modulators with low toxicity by combining the Cell Cycle Chromobody (CCC) technology with the CytoTox-Glo (CTG) cytotoxicity assay. The CCC technology employs intracellularly functional single-domain antibodies coupled to a fluorescent protein (chromobodies) to visualize the cell cycle–dependent redistribution of the proliferating cell nuclear antigen (PCNA) in living cells. This image-based cell cycle analysis was combined with determination of dead-cell protease activity in cell culture supernatants by the CTG assay. We adopted this multiplex approach to high-throughput format and screened 960 Food and Drug Administration (FDA)–approved drugs. By this, we identified nontoxic compounds, which modulate different cell cycle stages, and validated selected hits in diverse cell lines stably expressing CCC. Additionally, we independently validated these hits by flow cytometry as the current state-of-the-art format for cell cycle analysis. This study demonstrates that CCC imaging is a versatile high-content screening approach to identify cell cycle modulators, which can be multiplexed with cytotoxicity assays for early elimination of toxic compounds during screening.
- Is Part Of:
- SLAS discovery. Volume 21:Number 9(2016)
- Journal:
- SLAS discovery
- Issue:
- Volume 21:Number 9(2016)
- Issue Display:
- Volume 21, Issue 9 (2016)
- Year:
- 2016
- Volume:
- 21
- Issue:
- 9
- Issue Sort Value:
- 2016-0021-0009-0000
- Page Start:
- 965
- Page End:
- 977
- Publication Date:
- 2016-10
- Subjects:
- high-content screening -- chromobodies -- cell cycle -- multiplexing -- phenotypic drug discovery
Drugs -- Analysis -- Periodicals
Drugs -- Testing -- Periodicals
Biomolecules -- Analysis -- Periodicals
Biomolecules -- Analysis
Drugs -- Analysis
Drugs -- Testing
Drug Evaluation, Preclinical
Molecular Biology -- methods
Periodicals
Periodicals
615.1 - Journal URLs:
- http://journals.sagepub.com/home/jbx ↗
https://www.sciencedirect.com/journal/slas-discovery/ ↗
http://www.sagepublications.com/ ↗
https://www.journals.elsevier.com/slas-discovery ↗ - DOI:
- 10.1177/1087057116641935 ↗
- Languages:
- English
- ISSNs:
- 2472-5552
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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