The Problem
Detecting and measuring low-concentration toxins and biomarkers in environmental and human health settings with sufficient sensitivity for practical applications is challenging.
Research
A ‘Volume Dial’ for Missed Signals Produced by Our Bodies
System that monitors contaminants in drinking water now sensitive enough to detect tiny nucleic acids
Our Idea
Enhancing the sensitivity of a biosensing platform by adding genetic circuitry that amplifies weak molecular signals, enabling the detection of low-concentration toxins and biomarkers using cell-free synthetic biology.
Why It Matters
The breakthrough enables more sensitive, accurate, and accessible detection of harmful toxins, contaminants, and health markers at low concentrations, which has practical applications in environmental monitoring, disease diagnosis, and public health.
Our Team
Professor Julius Lucks, PhD candidate Jenni Li
An unplugged electric instrument may function, but it sounds much better when it is connected to an amplifier and pedals. Similarly, toxins and other small molecules at low concentrations in the environment or human body may emit quiet signals that are undetectable without specialized lab technology.
Now, thanks to a “cool trick in biochemistry” used to adapt a sensing platform already being deployed by Northwestern Engineering scientists to measure toxins in drinking water, researchers can detect and even measure chemicals at low enough concentrations to have use outside the lab. By attaching circuitry akin to a volume knob to “turn up” weak signals, the team opened the door for the system to be applied to disease detection and monitoring in the human body for nucleic acids like DNA and RNA, as well as bacteria such as E. coli.
The results, which describe a system that is 10 times more sensitive than previous cell-free sensors built by the team, were published January 13 in the journal Nature Chemical Biology.
“Biosensors repurposed from nature can, in principle, detect a whole spectrum of contaminants and human health markers, though they’re often not sensitive enough as is,” said corresponding author and Northwestern synthetic biologist Julius Lucks. “By adding genetic circuitry that acts like an amplifier, we can make this biosensing platform meet sensitivity levels needed for application in environmental and human health monitoring.”
Lucks is a professor of chemical and biological engineering at the McCormick School of Engineering and a co-director of the Center for Synthetic Biology
Engineering a ‘pregnancy test for water’
ROSALIND’s original model could sense 17 different contaminants in a single drop of water, glowing green when a contaminant exceeded the US Environmental Protection Agency’s standards. A second model enabled the platform to compute different concentrations of contaminants, creating something more sophisticated than a “pregnancy test for water.”
Lucks and his team used an approach called cell-free synthetic biology to create ROSALIND, in which molecular machinery – like DNA, RNA, and proteins – is removed from cells and then reprogrammed to perform new tasks.
A useful bug in the system
Synthetic biologists working with DNA and RNA often run into an unhelpful nemesis called T7 RNA polymerase enzyme, which Lucks compares to the radio battery for its role in pumping out output signals. For most, the enzyme can also act like a bug in the system, munching up snippets of RNA that it is not supposed to and wreaking havoc on nucleic acid circuits. But Lucks wondered if it could be used to their advantage.
Lucks uses the history of the transistor radio to explain advances in the sensing platform built by his team, which is called ROSALIND (named after famous chemist Rosalind Franklin and short for “RNA output sensors activated by ligand induction”).
“You could build the first transistor radio in your Electronics 101 class, and it gets a radio signal, but it has all sorts of problems,” Lucks said. “If you walk behind a tree, you will lose signal, and if you walk closer to the source, it will get louder. In future generations of that radio, they added additional electronic circuitry to control for and correct those things. This iteration is basically adding a volume knob to the radio.”
With a signal amplification trick from DNA nanotechnology that allows a circuit to recycle and replay its input, the researchers found a method to boost an input molecule’s signal. When a signal is generated, the “bug” eats and recycles it, generating another signal. The result allowed the team to detect molecules — like antibiotics and heavy metals — at a fraction of the concentration as previous iterations.
“We created a new system to amplify signals in ROSALIND,” said first author Jenni Li, a PhD candidate in the Lucks lab. “Due to a cool trick in biochemistry, this lets us sensitize the system to detect compounds at lower levels without changing the actual biosensor protein. This is all done in nucleic acid ‘circuits.’ ROSALIND 3.0 is now more sensitive and can detect nucleic acids when it could previously only detect small molecule compounds.”
ROSALIND at work
Previous iterations of ROSALIND are already deployed in real-world settings, for example, in an ongoing field study in the Chicago area detecting lead in drinking water. According to Lucks, new elements of the team’s “3.0” model can be easily applied to this and other projects.
“We are also developing ROSALIND to detect human health markers, food quality markers, and agricultural compounds, opening up what this platform technology can be used for,” Lucks said. “This new sensitization approach is general, meaning that we will more quickly be able to develop sensors that can detect compounds at actionable levels in the future.”