The graphic represents two laser traps holding two beads (gray spheres), which are stretching out the DNA (gray spirals on both sides) holding the telomerase protein/RNA machine (center, colored purple protein) and teal RNA. The telomerase extends the DNA on the right (which represents the end of a chromosome) and the newly created DNA (yellow) forms a loop extruding from the machine. Credit: Matthew Comstock

Stem cells involved in replenishing human tissues and blood depend on an enzyme known as telomerase to continue working throughout our lives. When telomerase malfunctions, it can lead to both cancer and premature aging conditions. Roughly 90% of cancer cells require inappropriate telomerase activity to survive.

In a groundbreaking new study, an interdisciplinary team of Michigan State University researchers has observed activity at a with unprecedented precision—expanding our understanding of the vital enzyme and progressing toward better cancer treatments.

This breakthrough was made possible by a novel investigative procedure and a pair of "optical tweezers," designed in close collaboration by coauthors Jens Schmidt, assistant professor in the Department of Obstetrics, Gynecology and Reproductive Biology, and Matthew Comstock, assistant professor in the Department of Physics and Astronomy and the Jerry Cowen Endowed Chair of Experimental Physics.

Optical tweezers use powerful lasers to create small forces capable of pushing, pulling and holding microscopic objects like individual strands of DNA and a telomerase enzyme.

"Our optical tweezer method lets us take the little machines out of the cell, gently hold onto them and watch them go," Comstock said. "By watching the telomerase work in real time, we can learn how it functions in full detail."

We know that as divide over time, the chromosomes gradually decrease in length. Each chromosome end is capped by a telomere—a disposable buffer of repeating DNA sequences.

Jens Schmidt (left) and Matthew Comstock (right) with the optical tweezers. Credit: Matthew Comstock

The telomerase enzyme attaches to the telomere buffer and replaces most of the sequences lost during replication. It was thought that telomerase made progressive extensions in a single step, but scientists could only theorize as to how it stayed in contact and aligned with the right sequence.

What the researchers found was essentially a safety harness anchored to the chromosome in a seemingly specific location.

"In an ideal world we could inhibit telomerase in without affecting stem ," Schmidt said. "This anchor site is a potential drug target. If we or someone else finds a molecule that interferes with the telomerase anchor site, telomerase would fall off the chromosome end faster, stopping its activity."

The team hopes their method and discovery will help others in their research.

"It is very important that we also are showing other teams with optical tweezer instruments like ours how to do these experiments," Comstock said.

For Schmidt and Comstock, this discovery is the realization of a long-term goal—it sets the stage for a wide range of new research opportunities. And most importantly, brings us one step closer to more effective and safe cancer treatments.

Both Schmidt and Comstock emphasized the unique partnership between their respective laboratories, with key efforts in the lab from Research Associate Dr. Eric Patrick and undergraduate researchers Joseph Slivka and Bramyn Payne. The pair credit this close relationship as a key factor in the discovery.

The study, "Observation of processive telomerase catalysis using high-resolution ," appears in Nature Chemical Biology.

More information: Eric M. Patrick et al, Observation of processive telomerase catalysis using high-resolution optical tweezers, Nature Chemical Biology (2020). DOI: 10.1038/s41589-020-0478-0

Journal information: Nature Chemical Biology