U-M scientists develop new tool to better understand neuronal signaling

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University of Michigan researchers have developed a new tool to better understand how chemicals like dopamine and epinephrine interact with neurons.

These chemicals are among a wide variety of signals that get processed in the brain through G protein-coupled receptors (GPCRs), proteins that sit on the surface of neurons to receive messages-;in the forms of proteins, sugars, fats, even light-;that inform cellular behavior. 

GPCRs are involved in an enormous number of biological functions, making them a prime target for treating diseases; more than one-third of FDA-approved drugs target GPCRs. But to fully understand how various molecules interact with GPCRs, researchers need to be able to detect those molecules across the whole brain with high spatial resolution.

The challenge in our field has been achieving the right balance between a detailed view and the whole picture across the brain."

Wenjing Wang, neuroscientist, U-M Life Sciences Institute

LSI faculty member Peng Li said most existing tools can detect a neural modulator either in a small part of the brain with high spatial resolution or in the whole brain with very low resolution.

"But we need to identify the cells that respond to the neuromodulators across various brain regions, in high resolution," he said.

In a study published in the Proceedings of the National Academy of Sciences, Wang, Li and colleagues unveiled a new chemical tool that achieves both goals for three chemicals that all target GPCRs.

Wang's lab at LSI uses protein engineering to develop technologies that can detect how signaling molecules travel within the brain to reach and interact with specific neurons. They previously created a tool to reveal the presence of opioids, another GPCR binding partner, at a cellular level.

When the molecule is detected, the tool creates a permanent fluorescent mark in the cells. Thus, researchers can see the specific cells that are highlighted, as well as the whole picture of cells across the brain.

This latest work broadens the utility of that sensor to detect multiple types of GPCR activators, beyond just opioids. So far, the team has tested the tool with opioids and epinephrine in cultured neurons and in mouse models. The team also expanded the tool to use both green and red fluorescence, enabling the tracking of multiple molecules at once.

"Coming from detecting just opioids, we now have a tool that we can begin to easily modulate for various signals that interact with GPCRs," said Wang, who also is an assistant professor of chemistry at the U-M College of Literature, Science, and the Arts. "The goal is eventually to even study the interplays of different signaling pathways simultaneously."

The team cautions that while the tool provides important visualizations of how signals travel across neurons for analysis postmortem, it cannot be used to track chemicals in real time, as it takes several hours for the fluorescence to appear. But it does offer a new path forward for improving understanding of neuronal signaling and the role of GPCRs as drug targets.

"Ideally, we aim to be able to create a brain map for multiple neuromodulators concurrently, offering a comprehensive understanding of the sites of neuromodulation," said Li, who also is an assistant professor at the U-M School of Dentistry.

Source:
Journal reference:

Kroning, K., et al. (2024). Single-chain fluorescent integrators for mapping G-protein-coupled receptor agonists. Proceedings of the National Academy of Sciences. doi.org/10.1073/pnas.2307090121.

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