The 50-nanometer tip of this nanoplasmonic fiber tip probe allows direct measurement of protein levels in living single cells. [Feng Liang, Ph.D., Rowland Institute, Harvard University]
The 50-nanometer tip of this nanoplasmonic fiber tip probe allows direct measurement of protein levels in living single cells. [Feng Liang, Ph.D., Rowland Institute, Harvard University]

Scientists from Massachusetts General Hospital (MGH) and the Rowland Institute at Harvard University have used a specialized nanoprobe developed by the Harvard/Rowland investigators to  measure levels of key proteins directly within living, cultured cells. As described in Nano Letters (“Direct Tracking of Amyloid and Tau Dynamics in Neuroblastoma Cells Using Nanoplasmonic Fiber Tip Probes”), the investigators used the device to track levels of the Alzheimer's-disease-associated proteins amyloid-β (Aβ) and tau in neurons and other cells exposed to an anesthetic known to produce Alzheimer's-like changes in the brains of mice. Their results support the view that the generation of Aβ is among the first steps leading to the characteristic neurodegeneration of Alzheimer's disease. 

“To study the dynamics of Aβ and tau, we needed a way to trigger the expression of both proteins and a tool to track dynamic changes of protein expression,” says lead author Feng Liang, Ph.D., a research fellow at the Rowland Institute. 

In 2008, some of the MGH members of the current team showed that the anesthetic isoflurane induced characteristic changes seen in Alzheimer's disease, including activation of cell-death enzymes and generation of Aβ, in cultured cells and in mouse brains. In 2014, the Harvard/Rowland researchers demonstrated the ability of their nanodevice to detect levels of intracellular proteins in living, cultured cells. The current study merges both of these accomplishments to investigate a key question regarding the mechanism of Alzheimer's disease: whether generation of Aβ precedes or follows the generation of the abnormal form of tau that characterizes the disease?

The tip of the device developed by the Harvard/Rowland investigators is around 50 nanometers (billionths of a meter) across, about 200 times smaller than a single cell. An integrated gold nanorod serves as the biosensor for surface plasmon resonance, an oscillation of electrons in response to a light signal that can generate an optical readout reflecting protein binding signals. Antibodies targeting specific proteins can be integrated into the probe to give specific measurements of protein levels. The team first demonstrated that it was possible to use the nanoplasmonic fiber tip probe (nFTP) to quantify protein levels in individual cells without affecting their vitality and viability. 

Using the nFTP device the investigators then tracked the changing levels of Aβ and the Alzheimer's-associated form of tau, which is characterized by excess phosphate molecules, in cultured cells that had been treated with isoflurane. The readings indicated that the increase in Aβ expression preceded the rise in phosphorylated tau levels by several hours.

The team then showed that, while blocking Aβ expression reduced tau levels, blocking tau did not prevent the initial rise in Aβ. However, without phosphorylated tau expression, Aβ levels eventually began to drop, suggesting a sequence in which Aβ generation stimulates tau phosphorylation, which promotes further generation of Aβ. 

“We have brought the traditional immunoassay into living cells with exquisite sensitivity,” says Qimin Quan, Ph.D., a junior fellow at the Rowland Institute and co-corresponding author of the Nano Letters report. “The device is still limited in its ability to measure a large number of single cells, requiring further improvement. But its high-sensitivity, label-free, and single-cell capability make it a unique tool for diagnosing clinically obtained limited samples.” 








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