If engineers at Stanford have their way, biological research may soon be transformed by a new class of light-emitting probes small enough to be injected into individual cells without harm to the host. Welcome to biophotonics, a discipline at the confluence of engineering, biology and medicine in which light-based devices – lasers and light-emitting diodes (LEDs) – are opening up new avenues in the study and influence of living cells. This is the first study to demonstrate that tiny, sophisticated devices known as light resonators can be inserted inside cells without damaging the cell. Even with a resonator embedded inside, a cell is able to function, migrate and reproduce as normal.
The researchers call their device a “nanobeam,” because it resembles a steel I-beam with a series of round holes etched through the center. This beam, however, is not massive, but measures only a few microns in length and just a few hundred nanometers in width and thickness. It looks a bit like a piece from an erector set of old. The holes through the beam act like a nanoscale hall of mirrors, focusing and amplifying light at the center of the beam in what are known as photonic cavities. These are the building blocks for nanoscale lasers and LEDs.
At the cellular level, a nanobeam acts like a needle able to penetrate cell walls without injury. Once inserted, the beam emits light, yielding a remarkable array of research applications and implications. While other groups have shown that it is possible to insert simple nanotubes and electrical nanowires into cells, nobody had yet realized such complicated optical components inside biological cells.
In this case, the studied cells came from a prostate tumor, indicating possible application for the probe in cancer research. The primary and most immediate use would be in the real-time sensing of specific proteins within the cells, but the probe could be adapted to sense any important biomolecules, such as DNA or RNA.
To detect these key molecules, researchers coat the probe with certain organic molecules or antibodies that are known to attract the target proteins, just like iron to a magnet. If the desired proteins are present within the cell, they begin to accumulate on the probe and cause a slight-but-detectable shift in the wavelength of the light being emitted from the device. This shift is a positive indication that the protein is present and in what quantity.
“Let’s say you have a study that is interested in whether a certain drug produces or inhibits a specific protein. Our biosensor would tell definitively if the drug was working and how well, based on the color of the light from the probe. It would be quite a powerful tool,” explained Sanjiv Sam Gambhir, chair of the Department of Radiology at the Stanford School of Medicine as well as director of Stanford’s Canary Center for Cancer Early Detection.
As such, embeddable nanoscale optical sensors would represent a key development in the quest for patient-specific cancer therapies – often referred to as personalized medicine – in which drugs are targeted to the patient based on efficacy.
Structurally, the new device is a sandwich of extremely thin layers of the semiconductor gallium arsenide alternated with similarly thin layers of light-emitting crystal, a sort of photonic fuel known as quantum dots. The structure is carved out of chips or wafers, much like sculptures are chiseled out of rock. Once sculpted, the devices remain tethered to the thick substrate. For biological applications, the thick, heavy substrate presents a serious hurdle for interfacing with single cells. The underlying and all-important nanocavities are locked in position on the rigid material and unable to penetrate cell walls.
The breakthrough came when Gary Shambat, a doctoral candidate in electrical engineering, was able to peel away the photonic nanobeams. He then glued the ultrathin photonic device to a fiberoptic cable with which he steers the needlelike probe toward and into the cell. Once inserted in the cell, the probe emits light, which can be observed from outside. For engineers, it means that almost any application of these powerful photonic devices can be translated into the previously off-limits environment of the cell interior.
In one finding that the researchers describe as stunning, they loaded their nanobeams into cells and watched as the cells grew, migrated around the research environment and reproduced. Each time a cell divided, one of the daughter cells inherited the nanobeam from the parent and the beam continued to function as expected. This inheritability frees researchers to study living cells over long periods of time, a research advantage not possible with existing detection techniques, which require cells be either dead or fixed in place.
“Our nanoscale probes can reside in cells for long periods of time, potentially providing sensor feedback or giving control signals to the cells down the road,” said Shambat. “We tracked one cell for eight days. That's a long time for a single-cell study.”
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