Single-Molecule Valve: A Breakthrough in Nanoscale Control

A joint research group at Osaka Metropolitan University has succeeded in regulating the flow of single molecules in solution by opening and closing the nanovalve mounted on the nanofluidic device by applying external pressure. The research group fabricated a device with a ribbon-like, thin, soft glass sheet on the top, and at the bottom a hard glass substrate having nanochannels and nanovalve seats. By applying external pressure to the soft glass sheet to open and close the valve, they succeeded in directly manipulating and controlling the flow of individual molecules in solution. They also observed an effect of fluorescence signal amplification when single fluorescent molecules are confined in the tiny nanospace inside the valve. The effect can be ascribed to the nanoconfinement, which suppresses the random motion of the molecules.

Schematic drawing of the working principle of the single-molecule valve

Scientists dream of using tiny molecules as building blocks to construct things, similar to how we build things with mechanical parts. However, molecules are incredibly small - around one hundred millionth the size of a softball - and they move randomly in liquids, making it very difficult to manipulate them in a single form. To overcome this challenge, “nanofluidic devices” that can transport molecules in extremely narrow channels, similar in size to one millionth of a straw, are attracting attention as a way to directly manipulate single molecules in solutions.

A joint research team led by Associate Professor Yan Xu of the Osaka Metropolitan University Graduate School of Engineering has succeeded in regulating the flow of single molecules in solution by opening and closing a nanovalve in a nanofluidic device by applying external pressure.

The research team fabricated a nanofluidic device with a thin, flexible glass sheet on the top, and a hard glass plate with small structures that forms nanochannels and nanovalve seats on the bottom. By applying external pressure to the flexible glass sheet to open and close the valve, they succeeded in directly manipulating and controlling the flow of individual molecules in solution. They also found that when they trapped single fluorescent molecules in the nanospace inside the valve, the fluorescence of the single molecules became brighter. This happened because the small space made it harder for the single molecules to move around randomly. Professor Xu said that “this effect of fluorescence signal amplification could help with detecting very small amounts of pathogens for early diagnosis of diseases such as cancers and Parkinson's disease, without requiring expensive equipment.”

The findings of this study could be a significant step towards freely assembling materials using single molecules as building blocks in solution. This technology has the potential to be useful in various fields, such as developing personalized medicines for rare diseases and creating better displays and batteries. Its applications are limitless.

“We have been addressing various challenges by proposing and promoting the concept of ‘Single-Molecule Regulated Chemistry (SMRC),’ where molecules are treated as building blocks and all processes involved in chemical and biochemical reactions in solution are performed on a single-molecule basis. The single-molecule valve marks the first step towards the goal, which could one day revolutionize chemistry, biology, and materials science, as well as transform various industries,” said Professor Xu.

Their findings were published in Nano Letters.

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Conflict of interest 

The authors declare no conflict of interest. 

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Published: 02 May 2023

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Rina Matsuki

3-3-138 Sugimoto, Sumiyoshi-ku,
Osaka 558-8585 JAPAN

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Title: Flexible glass-based hybrid nanofluidic device to enable the active regulation of single-molecule flows
DOI: 10.1021/acs.nanolett.2c04807
Author: Hiroto Kawagishi, Shun-ichi Funano, Yo Tanaka, Yan Xu
Publish: March 6,2023
URL: https://doi.org/10.1021/acs.nanolett.2c04807

Funding information:

This work was partially supported by JSPS KAKENHI (Grant Nos. JP21H04640, JP20H00497, JP19KK0129, JP18H01848, JP26630403 and JP19J22901), MEXT KAKENHI (Grant Nos. JP21H05231 and JP19H04678), JST PRESTO (Grant No. JPMJPR18H5), JST CREST (Grant No. JPMJCR18H2), and SiMS of Osaka Prefecture University.