Scientists have created a new protein that can capture the incoming chemical signals received by brain cells, not just the signals they send out. These incoming messages are carried by glutamate, a neurotransmitter that plays a central role in brain communication. Although glutamate activity is essential for how the brain functions, its signals are extremely subtle and fast, making them nearly impossible to observe until now.
This breakthrough allows researchers to record these faint chemical messages as they arrive at individual neurons, opening a new window into how the brain processes information.
Why this breakthrough matters
By detecting incoming signals, scientists can now explore how neurons actually compute information. Each neuron integrates thousands of inputs before producing an output, a process that underlies thinking, decision making, and memory. Being able to observe this process directly could help explain long-standing questions about how the brain works.
The discovery also has important implications for disease research. Abnormal glutamate signaling has been linked to conditions such as Alzheimer’s disease, schizophrenia, autism, and epilepsy. Having tools that can track these signals more precisely may help researchers identify what goes wrong in these disorders.Drug development could benefit as well. Pharmaceutical researchers can use these sensors to see how experimental treatments affect real synaptic activity, potentially speeding up the development of more effective therapies.
A new protein that listens to neurons
The protein, developed by scientists at the Allen Institute and HHMI’s Janelia Research Campus, is a molecular “glutamate indicator” known as iGluSnFR4 (pronounced ‘glue sniffer’). It is sensitive enough to detect the weakest incoming chemical signals exchanged between neurons.
By revealing when and where glutamate is released, iGluSnFR4 offers a new way to interpret the complex patterns of activity that support learning, memory, and emotion. Researchers can now observe neurons communicating inside the brain in real time, rather than inferring activity indirectly. The findings were recently published in Nature Methods and could significantly change how neural activity is measured and analyzed in neuroscience research.
High-speed video of cultured neurons expressing iGluSnFR3 (100 Hz, measured on a simple widefield microscope). Neurons have been silenced with TTX, blocking evoked glutamate release. The flashes are iGluSnFR3 responding to spontaneous release of individual vesicles, on average containing just 500 molecules of glutamate. Credit: Allen Institute
How neurons communicate inside the brain
To appreciate the importance of this advance, it helps to understand how brain cells interact. Billions of neurons communicate by sending electrical pulses down long, branch-like structures called axons. When an electrical signal reaches the end of an axon, it cannot cross the tiny gap to the next cell, known as a synapse.
Instead, the signal triggers the release of chemical messengers called neurotransmitters into the synapse. Glutamate, the most common neurotransmitter in the brain, is especially important for memory, learning, and emotion. When glutamate reaches the next neuron, it can cause that cell to fire and pass the signal along.
This process resembles a chain reaction, but it is far more intricate. Each neuron receives input from thousands of others, and only specific combinations and patterns of those inputs determine whether the receiving neuron activates. With this new protein sensor, scientists can now identify which patterns of incoming signals lead to neuronal firing.










