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Updated: Jun 19, 2026

High Throughput, Real-time, Dual-readout Testing of Intracellular Antimicrobial Activity and Eukaryotic Cell Cytotoxicity
Published on: November 16, 2016
A novel no-wash (homogenous) high-throughput toxicity assay on primary cells
Yan Cheng1, Victoria S Yang2, Zixuan Zhu3
1Dexorgen, Inc., 12358 Parklawn Drive, Suite 250A, USA.
Abstract:
Mitochondrial membrane potential (MMP) is a critical marker of mitochondrial and, therefore, cellular function. However, current dyes used for MMP measurement possess significant limitations: nonspecific targeting, long incubation times, potential mitochondrial toxicity, poor water solubility, and numerous wash steps. Using a novel fluorescent dye-mitochondrial membrane potential indicator (m-MPI)-in combination with a masking dye, we overcame these challenges and successfully measured MMP changes across multiple cell lines and four different human primary cells. This no-wash assay has been miniaturized into a 384-well format. It is robust, with a Z' value > 0.5 on both HepG2 and HeLa cells, making it suitable for high-throughput screening. The reagents in the m-MPI homogeneous assay kit are non-toxic, as was demonstrated in HepG2 and HeLa cell lines using Dexorgen's EnerCount ATP assay. Using this assay, we conducted a pilot screen on human hepatocytes against the Library of Pharmacologically Active Compounds (LOPAC) (Sigma). Identified hits were subsequently confirmed through follow-up studies. Collectively, these findings establish the m-MPI assay as a reliable, scalable tool for mitochondrial functional analysis and drug discovery.
Insights
A new assay using a novel fluorescent dye (m-MPI) accurately measures mitochondrial membrane potential (MMP) in cells. This non-toxic, no-wash, high-throughput method offers a reliable tool for cellular function analysis and drug discovery.
Area of Science:
- Biochemistry
- Cell Biology
- Pharmacology
Background:
- Mitochondrial membrane potential (MMP) is crucial for cellular function.
- Existing MMP measurement dyes have limitations including toxicity and complex protocols.
Purpose of the Study:
- To develop a novel, improved assay for measuring MMP.
- To overcome limitations of current MMP detection methods.
Main Methods:
- Developed a novel fluorescent dye, mitochondrial membrane potential indicator (m-MPI), with a masking dye.
- Validated the assay in multiple cell lines and human primary cells.
- Miniaturized the assay into a 384-well, no-wash, high-throughput format.
Main Results:
- The m-MPI assay successfully measured MMP changes across various cell types.
- The assay demonstrated robustness with Z' values > 0.5, suitable for high-throughput screening.
- Reagents were confirmed non-toxic using an ATP assay.
Conclusions:
- The m-MPI assay is a reliable and scalable tool for mitochondrial function analysis.
- This assay facilitates drug discovery through efficient screening of compounds.
- The developed assay overcomes significant limitations of previous MMP measurement techniques.
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