Polymers are long, chain-like molecules which are everywhere in biology. DNA and RNA are polymers formed by many consecutive copies of nucleotides coupled together. When being transported within or between cells, these biological polymers must pass through nanometre-sized holes called “nanopores”.This process also underlies a rapidly developing method for analyzing and sequencing DNA called nanopore sensing.
The experimental results revealed a two-step process where the DNA speed initially slows down before accelerating close to the end of the translocation. Simulations also demonstrated this two-stage process and helped to reveal that the underlying physics of the process is determined by changing friction between the DNA and surrounding fluid.
Our method for assembling LEGO-like molecular DNA rulers has given new insight into the process of threading polymers through incredibly small holes just a few nanometres in size. The combination of both experiments and simulations have revealed a comprehensive picture of the underlying physics of this process and will aid the development of nanopore-based biosensors. It is very exciting that we can now measure and understand these molecular processes in such minute detail.
These results will help improve the accuracy of nanopore sensors in their various applications, for instance localizing specific sequences on DNA with nanometer accuracy or detecting diseases early with target RNA detection. The superior resolution in analyzing molecules passing through nanopores will allow for low-error decoding of digital information stored on DNA. We are exploring and improving the utility of nanopore sensors for these applications.
Kaikai Chen et al, Dynamics of driven polymer transport through a nanopore, Nature Physics (2021). DOI: 10.1038/s41567-021-01268-2