To undergo high-resolution imaging, cells often must be sliced and diced, dehydrated, painted with toxic stains, or embedded in resin. For cells, the result is certain death.
But if researchers can only view the inner workings of dead cells, they’re only seeing part of the story. They cannot monitor living cells’ dynamic real-time processes, such as metabolic reactions or responses to diseases or treatments.
“Sub-cellular components and structures have a profound influence on the behavior of the complex cellular machinery and systems biology,” said Northwestern Engineering’s Gajendra Shekhawat. “However, unraveling the structures and components inside the cell is very challenging because they are so fragile.”
Now Shekhawat and Vinayak P. Dravid, the Abraham Harris Professor of Materials Science and Engineering, have developed a novel non-invasive imaging system that makes it possible to view the sub-cellular architecture of live cells at nanometer-scale resolution. Called Ultrasound Bioprobe, the technique combines ultrasound waves with atomic force microscopy, interacting with live cells to determine the changes in their mechanical behavior.
Supported by the National Science Foundation (NSF) and the National Heart, Lung, and Blood Institute, the research was recently published in Science Advances. Shekhawat and Dravid served as the paper’s co-corresponding authors. Shekhawat, a research associate professor in materials science and engineering, was also the first author of the paper. The research was completed in the Northwestern University Atomic and Nanoscale Characterization Experimental (NUANCE) Center. NUANCE is the lead facility in the NSF-supported National Nanotechnology Coordinated Infrastructure (NNCI) Program, which is headquartered at Northwestern and called the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource.
Despite recent advances in imaging, there is currently no single method that provides high-resolution and high-sensitivity images of living sub-cellular structures. Fluorescent and confocal microscopy, which are traditional methods for monitoring the biological interactions inside cells, suffer from poor spatial resolution and require invasive dyes or labels to enhance contrast and highlight structures within biological tissues. Light and acoustic wave imaging are unable to view structures smaller than a few hundred nanometers. Scanning probe microscopy can provide very high spatial resolution but can only identify surface structures rather than peer inside a cell. And while electron microscopy can view fine details at the sub-cellular level, it’s a destructive technique that cannot be used for living biological tissues.
“Many roadblocks have existed,” said Dravid, who directs the NUANCECenter and the SHyNE Resource. “Characterization of the complex dynamics of biological processes, especially signal pathways at nanoscale resolution, has remained a challenge.”
Shekhawat and Dravid’s Ultrasound Bioprobe, however, bypasses these issues. Its ultrasound waves non-invasively image deeply buried intracellular features. And its atomic force microscopy probe provides high sensitivity and mechanical contrast of the scattered ultrasound waves. The result? Non-destructive, remarkably high-contrast, nanoscale images of structures and components deep inside living tissues and cells.
“Using this non-invasive approach, we can monitor real-time imaging of the nanomechanical changes in complex biological systems,” Shekhawat said. “This could provide clues for early diagnostics and potential pathways for developing therapeutic strategies.”
Next, the team plans to expand its technique to diverse biomedical applications, such as the nanomechanics of soft tissues such as skin, enamels, and bones to probe their three-dimensional architecture down to nanoscale spatial resolution.
“A significant variation in cellular nanostructures and mechanics can be directly influenced by the cancer conditions of a cell,” Dravid said. “So Ultrasound Bioprobe could also expand our fundamental understanding of the nanomechanics at play within cancer cells.”