Researchers at the University of California, Lawrence Berkeley National Laboratory and Marine Biological Laboratory, have created a cellular probe that combines a tarantula toxin with a fluorescent compound to help scientists observe electrical activity in neurons and other cells. The probe binds to a voltage-activated potassium ion channel subtype, lighting up when the channel is turned off and dimming when it is activated.
This is the first time researchers have been able to visually observe these electrical signalling proteins turn on without genetic modification. These visualization tools are prototypes of probes that could some day help researchers better understand the ion channel dysfunctions that lead to epilepsy, cardiac arrhythmias and other conditions.
Ion channels have been called life’s transistors because they act like switches, generating electrical feedback. To understand how neural systems or the heart works, the medical community need to know which switches are activated. These probes tell us when certain switches turn on.
Voltage-gated channels are proteins that allow specific ions, such as potassium or calcium, to flow in and out of cells. They perform a critical function, generating an electrical current in neurons, muscles and other cells. There are many different types, including more than 40 potassium channels. Though other methods can very precisely measure electrical activity in a cell, it has been difficult to differentiate which specific channels are turning on.
There are about 40 voltage-gated potassium channel genes that are basically doing the same thing, and it’s been shockingly hard to figure out which ones are doing something that’s physiologically relevant state the team.
The tarantula toxin, guangxitoxin-1E, was an ideal choice because it naturally binds to the Kv2 channels. These channels are expressed in most, if not all, neurons, yet their regulation and activity are complex and actively debated.
To study the channels, the team engineered variants of tarantula toxin that could be fluorescently labelled and retain function. These probes were designed to bind to the potassium channels when they were at rest and let go when they became active. The researchers then tested them on living cells. To their surprise, the probes worked right away giving a very clear signal. When the team then added potassium to stimulate the cells, the probes fell right off.
While this is just a first step towards imaging the activity of potassium and possibly other ion channels, this approach holds vast potential to help scientists understand the underlying mechanisms behind cardiac arrhythmias, muscle defects and other channelopathies.
There are dozens of known channelopathies, and more being uncovered at an increasing pace. If there is electrical signalling, then there is a potassium channel, and when that channel goes bad, the cell doesn’t work the same anymore. For example, the Kv2.1 channel that this probe binds to leads to epilepsy when it’s not functioning properly.
In addition, the ability to better observe electrical signalling could help researchers map the brain at its most basic levels. Understanding the molecular mechanisms of neuronal firing is a fundamental problem in unravelling the complexities of brain function.
While creating a probe that can read whether the Kv2.1 channel is firing or at rest is an important proof-of-concept, there’s still a lot of work to be done. The researchers will continue to collaborate, testing other types of spider venom that bind to different potassium channels.
The team state that this is a toehold into a new way of visualizing electrical activity with a huge family of spider toxins to target different ion channels. The potential here is enormous.
Source: UC Davis Health System
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