Figure 1 – Smaller, lighter, cost-effective: The EPR spectrometer by Bridge 12 opens this technology to many more scientists
Thorsten Maly, VP Magnetic Resonance at Bridge12, said, “As a start-up, we had a clean slate to design our EPR spectrometer enabling us to use the latest technologies to create a next generation product that is much more compact than existing products. This will open up the use of this methodology to a much greater audience of researchers. Most of our customers are university researchers who gain access to the method through collaborations. Having a cheaper, state-of-the-art instrument will increase access to this powerful method. Our third goal was to make it much easier to use than current devices that need an experienced operator so that any scientist can use it for their research which will make EPR spectroscopy more widely used. Our control software has been designed to be intuitive to use with many features automated so that the set-up is straightforward and it immediately shows if the experiment is working correctly. You don’t have to be an expert in EPR spectroscopy to obtain results.”
How EPR works
An example of where EPR spectroscopy can be used is in structural biology to determine distances between radicals to determine the folded shape of (membrane) proteins. This provides insights on how these proteins can interact with other molecule or proteins. This is done by attaching two spin labels (markers) to the protein and measuring their distance using pulsed dipolar spectroscopy, a form of pulse EPR spectroscopy. The spin labels are specially designed, non-reactive, radical molecules that EPR spectroscopy can detect by exciting the radical with a sequence of microwave pulses and detecting the response. The dipolar coupling between the spins directly leads to the distance between the two markers. Spin label pairs can be put in different places on the protein to generate a set of distances that can be used to determine the three-dimensional model of how the protein is folded.
Operation in the 35 GHz Q band range
EPR spectroscopy has evolved over the past few decades thanks to advances in radar technology and the mobile telecommunications that created equipment that could be used to build EPR hardware which uses microwave technology that needs increasingly higher frequencies for better resolution. Historically, EPR spectrometers have operated at 10 GHz (X-Band), but thanks to 5G technology, there is now new commercial equipment that can operate at much higher frequencies such as 35 GHz (Q band), a frequency that is much more desired for this type of application.
The AWG generates 10 – 100 ns long pulses in the 200 to 500 MHz range as required by the experiment that are then first up-converted to X band range using an RF I/Q mixer and then up-converted to the Q band range. The microwave pulses are then fed into 100 W solid-state amplifier before sent to the EPR resonator. The reflected signal is then down-converted to an IF frequency in the 200 to 500 MHz range and sent to the digitizer. In EPR spectroscopy, the signal is traditionally down-converted to DC, however this new approach drastically reduces noise and artifacts.
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