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Fluorescent Sensor Detects Drug-Induced Protein Stress in Cells

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A fluorescent sensor that will become activated in a cell when misfolded proteins in the cell begin to aggregate could be an effective way to detect drug-induced proteome stress prior to cell death.

Researchers from Penn State University have designed an unstable protein, called AgHalo, to sense proteome stress through the protein’s aggregation. AgHalo was tagged with a fluorogenic ligand that fluoresced when AgHalo formed soluble aggregates. When the AgHalo protein began to misfold and aggregate, the dye interacted with the hydrophobic portions of the protein and began to fluoresce.

AgHalo sensor developed to detect protein stress in cells, Penn State University.

Image of cells expressing the AgHalo sensor before (left) and after (right) cellular stress. The AgHalo sensor is turned on when misfolded proteins begin to aggregate and provides a quantitative measure of cellular stress that can be used to evaluate drug safety. Courtesy of Yu Liu, Penn State University.

The researchers used their sensor to test the level of protein stress caused by five commonly-used anti-cancer drugs. All five produced some level of protein stress detectable by the AgHalo sensor before any cell death was observed.

“Because we tested the anti-cancer drugs at much higher doses than typically used for treatment, our results do not necessarily call into question the continued use of these drugs,” said researcher Yu Liu. “However, because protein stress from long-term treatments could have lasting effects, evaluating drugs with our new sensor will help in the development of safer drugs.”

Drug safety is regularly evaluated using cytotoxicity assays that measure cell death. However, these assays provide limited insights into the presence of proteome stress in live cells. According to the researchers, previous systems have used sensors that were always “on.” The cells would have a diffuse fluorescence prior to any stress, and the system could only detect protein stress when misfolded proteins aggregated, forming bright spots of fluorescence that were large enough to be seen under a microscope.

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“An additional advantage of our system is that the level of fluorescence is correlated to the amount of protein aggregation in the cell, so we can quantify the level of stress,” said Liu. “Also, because our method measures the level of fluorescence, rather than having to identify the fluorescence under a microscope, it can be done using more accessible technology, like plate readers, and it is much more high-throughput.”

Professor Xin Zhang said, “Drug-induced protein stress in cells is a key factor in determining drug safety. Drugs can cause proteins — which are long strings of amino acids that need to be precisely folded to function properly — to misfold and clump together into aggregates that can eventually kill the cell. We set out to develop a system that can detect these aggregates at very early stages and that also uses technology that is affordable and accessible to many laboratories.”

Heat, toxins, bacterial infections, cancer and even aging can cause protein stress.

“With our method, we can quantitatively detect protein stress in cells at much earlier stages and therefore researchers can begin to study the mechanisms that cells use to combat this stress and develop compounds that can enhance the cell’s ability to handle protein stress,” said Zhang.

The research was performed at Penn State University. The research was published in Angewandte Chemie International Edition (doi: 10.1002/ange.201702417).  

Published: August 2017
Glossary
fluorescence
Fluorescence is a type of luminescence, which is the emission of light by a substance that has absorbed light or other electromagnetic radiation. Specifically, fluorescence involves the absorption of light at one wavelength and the subsequent re-emission of light at a longer wavelength. The emitted light occurs almost instantaneously and ceases when the excitation light source is removed. Key characteristics of fluorescence include: Excitation and emission wavelengths: Fluorescent materials...
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