News Release

Deep learning for real-time molecular imaging

Peer-Reviewed Publication

National University of Singapore

Figure 1

image: 

(a) FCSNet is a convolutional neural network (CNN), which takes in the autocorrelation function Gτ  of a measurement as an input to predict the diffusion coefficient. (b) FCSNet allows evaluations in complex samples with a precision as good, or better than traditional Imaging FCS methods, as shown by the heatmaps.

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Credit: Biophysical Journal

National University of Singapore (NUS) researchers have demonstrated that deep learning allows them to observe the dynamics of single molecules more precisely and with less data than traditional evaluation methods. They used convolutional neural networks (CNNs) to observe the movement of single molecules in artificial systems, cells and small organisms. This method promises to accelerate single-molecule measurements in complex systems and make it more accessible to a wider range of researchers.

A single molecule is the most basic unit observable in biological systems. Understanding its behaviour and interactions unlocks insights into the functioning of biological systems, paving the way for strategic interventions in diseases. One of the most powerful ways to observe single molecules is fluorescence spectroscopy. This is due to its strong signal and specificity, which allows only labelled molecules to be observed. For over 50 years, Fluorescence Correlation Spectroscopy (FCS) has been used in this field, measuring the mobility and interaction of molecules with high accuracy and precision. A recent extension of this technique, Imaging FCS, extends its capabilities to characterise mobilities, concentrations and interactions among other parameters in whole images. Despite its capabilities, Imaging FCS poses challenges as it requires large amounts of data (about 100 MB for every measurement). This requires extensive computational processing, which results in slow evaluations.

A research team, led by Professor Thorsten WOHLAND from the NUS Department of Biological Sciences and Department of Chemistry, and Professor Adrian RÖLLIN, from the NUS Department of Statistics and Data Science, used deep learning methods to reduce the amount of data required for a measurement (about 5 MB per measurement) while achieving comparable results to traditional methods. The technique uses two CNNs, called FCSNet and ImFCSNet developed by Dr Wai Hon TANG and Mr Shao Ren SIM, members of the NUS research team. CNNs represent a type of deep learning algorithm suited for analysing visual data. They employ multiple layers of specialised filters that scan across the image for specific features, such as edges, textures and colours. By progressively extracting and combining these features together, they build up a better understanding of the image, allowing them to recognise patterns and objects within the visual data.

Both the FCSNet and ImFCSNet based methods are more precise than traditional FCS methods in terms of diffusion coefficients, but they have different trade-offs for data requirements and spatial resolution. By utilising less data, these techniques can potentially shorten the evaluation time by orders of magnitude, especially for large datasets or complex systems.

Their findings were published in the Biophysical Journal on 4 December 2023.

Prof Wohland said, “These CNNs are trained on simulated data and can predict diffusion coefficients from much smaller datasets compared to traditional FCS methods. They are also model agnostic and can be used with any microscope setup.”

Dr Tang added, "CNNs revolutionise data analysis, offering accelerated and simplified evaluation processes. While it is important to validate their performance, CNNs have the potential to make powerful techniques available to the wider research community."

The team hopes that their technique can open new possibilities to accelerate single-molecule research and make the technology accessible to a wider range of users. The CNNs do not require expert inputs and are poised to democratise FCS.


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