Tracking molecules at turbo speed

January 15, 2024 This article has been reviewed according to Science X's editorial process and policies . Editors have highlighted the following attributes while ensuring the content's credibility: fact checked peer reviewed publication trusted source proofread by Katrin Piecha, University of Bonn Microbiologists and biophysicists from the University of Bonn have developed a method that makes the high throughput process for observing molecules five times faster, enabling insights to be gained into hitherto unknown cellular functions.

UV rays can cause mutations in our DNA, which can potentially lead to cancer. However, the human body has a defense mechanism that it can deploy. "Damage to our DNA activates molecules that repair it quickly, ideally before the cell divides and the damage spreads," explains Koen Martens from the Institute for Microbiology and Biotechnology at the University of Bonn.

Yet nobody quite knows exactly how fast this cellular repair function works, something that Martens now wants to find out. This is easier said than done, however, as the methods used to date are not powerful enough to track individual molecules accurately. "Single particle tracking involves marking the molecule with fluorescent light, making it into a kind of light bulb ," Martens explains.

"We then take hundreds of photos a second using a high resolution microscope. Our 'light bulb' lights up the molecule in the darkness of the cell, allowing us to observe it and track its movement over time. This enables us to measure its diffusion and how it interacts with other cellular components." By looking at the gaps between molecules and the distances traveled by a single molecule from one photograph to another, the researchers can tell whether the particles are moving freely inside the cell or interacting with other molecules.

As far as DNA repair is concerned, this indicates when the enzymes are performing their repair work —when they are interacting with the DNA—and when they are "idle," i.e., diffusing freely inside the cell. However, the method does have one drawback. "It's hard to track multiple molecules at the same time," Martens explains.

"When their paths cross or they're too close together, you get two light bulbs merging, in effect. Then it's impossible to identify their movements." Up until now, therefore, microbiologists have had to study molecules one after the other in a time consuming process that is too long winded to observe the DNA repairing molecules "at work." In fact, single particle tracking currently takes longer than the repair process itself.

To solve the problem, Martens has created a piece of software to speed up the high throughput process. TARDIS (short for "temporal analysis of relative distances") runs an all to all analysis of the distances between locations, i.e. the positions of the molecule in the individual photographs, with increasing time lags.

The work has been published in Nature Methods . Instead of focusing on individual points as before, it looks at the entire sequence of movements within the cell and thus scrutinizes all the molecules simultaneously. "TARDIS makes the measurement process at least five times faster without any loss of information," says Martens.

This means that he can now devote his attention to the remaining part of his research project, using TARDIS to study the processes involved in DNA repair in more detail. "I'm especially interested in investigating how easy or difficult certain kinds of damage are to repair and how badly the DNA is damaged by a specific dose of UV radiation or chemicals," Martens says.

More information: Koen J.A. Martens et al, Temporal analysis of relative distances (TARDIS) is a robust, parameter free alternative to single particle tracking. Nature Methods (2024). DOI: 10.1038/s41592 023 02149 7 Journal information: Nature Methods Provided by University of Bonn.