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Tagging Tiny Proteins To Probe Roots of Depression

Tagging Tiny Proteins To Probe Roots of Depression Scientists at Vanderbilt University have managed to tag a protein that regulates the neurotransmitter serotonin with tiny fluorescent beads, allowing them to track the movements of single molecules for the first time.

The capability, which took nearly a decade to achieve, makes it possible to study serotonin regulation at a new level, which is important because of the key role that serotonin plays in the regulation of mood, appetite and sleep, according to the researchers.

The regulatory protein that the scientists successfully tagged is known as the serotonin transporter. It extends through the membrane that forms the nerve’s outer surface and acts like a vacuum cleaner that sucks serotonin molecules into the cell body and away from serotonin target receptors on other cells, regulating the concentration of serotonin in the area around the cell.

Serotonin transporters are an important research subject because they are the target for the most common drugs used to treat depression, including Prozac, Paxil and Lexapro, the researchers note.

“If you are interested in mental health, then serotonin transporters are an ideal subject,” said Sandra Rosenthal, Ph.D., the Jack and Pamela Egan Chair of Chemistry, who directed the study with Randy Blakely, Ph.D., the Allan D. Bass Professor of Pharmacology and Psychiatry.

The researchers noted that problems with serotonin transporter regulation have also been implicated in autism. Two years ago, Blakely and geneticist James Sutcliffe reported the discovery of multiple changes in the serotonin transporter protein that cause the transporter to become “overactive” in people with autism.

Recently, Blakely and Jeremy Veenstra-VanderWeele, M.D., reported that mice expressing one of these high-functioning transporters exhibit multiple behavioral changes that resemble changes seen in kids with autism.

Attempts to understand how these transporters work have been limited by the difficulty of studying their behavior, according to the scientists.

“In the past, we have been limited to snapshots that show the location of transporter molecules at a specific time,” said chemistry graduate student Jerry Chang, who developed the tagging technique. “Now we can follow their motion on the surface of cells in real time and see how their movements relate to serotonin uptake activity.”

The fluorescent tags the researchers used are nanoscale beads called quantum dots made from a mixture of cadmium and selenium. The beads are only slightly bigger than the proteins they are tagging: You would have to string 10,000 together to span the width of a human hair, the researchers explain.

Quantum dots emit colored light when illuminated and small changes in their size cause them to glow in different colors. One of the researchers, Ian D. Tomlinson, Ph.D., developed a special molecular string that attaches to the quantum dot at one end and attaches to a drug derivative on the other end that binds with the serotonin transporter.

When a mixture that contains these quantum dots is incubated with cultured nerve cells, the drug attaches to the transporter. As the protein moves around, it drags the quantum dot behind it like a child holding a balloon on a string, he explained. When the area is illuminated, the quantum dots show up in a microscope as colored points of light.

Putting their new procedure to use, the researchers looked at extensions of the nerve cell that are involved in secreting serotonin. From previous research, the researchers suspected that the transporters would be concentrated in cholesterol-rich parts of these extensions, termed rafts, although the level of resolution with standard approaches was inadequate to provide any clues as to what they were doing there.

The quantum dot studies demonstrated that there were two distinct transporters: those that can travel freely around the membrane and those that act as if they are unable to move. They found that the immobile transporters were located in the rafts.

When they stimulated the cell to increase transporter activity, they were surprised at what happened. “We found that the transporters in the rafts began to move much faster, whereas the motion of the other population didn’t change at all,” Rosenthal reported.

Since the mobilized transporters do not leave the rafts, they appear to whiz around inside a confined compartment, as if released from chains that normally keep them subdued. These observations suggest it is likely that the two populations are controlled by different regulatory pathways.

“Now that we can watch transporter regulation actually happening, we should be able to figure out the identity of the anchoring proteins and the signals these proteins respond to that permit transporters to switch back and forth between low and high activity levels,” said Blakely.

“Currently, antidepressant drugs must fully shut down the brain’s serotonin transporters to achieve a clinical benefit,” he added, noting that this can produce a number of unpleasant side-effects, such as nausea, weight gain, sexual problems, fatigue and drowsiness.

“By understanding the basic mechanisms that naturally turn serotonin transporter activity up and down, maybe we can develop medications that produce milder side effects and have even greater efficacy,” he said. “Our sights are also focused on transferring what we have learned with normal serotonin transporters to an understanding of the hyperactive transporters we have found in kids with autism.”

Source: Vanderbilt University

Tagging Tiny Proteins To Probe Roots of Depression

Janice Wood

Janice Wood is a long-time writer and editor who began working at a daily newspaper before graduating from college. She has worked at a variety of newspapers, magazines and websites, covering everything from aviation to finance to healthcare.

APA Reference
Wood, J. (2018). Tagging Tiny Proteins To Probe Roots of Depression. Psych Central. Retrieved on November 28, 2020, from
Scientifically Reviewed
Last updated: 8 Aug 2018 (Originally: 5 Jul 2012)
Last reviewed: By a member of our scientific advisory board on 8 Aug 2018
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