FLUIDFM SINGLE CELL EXTRACTION

Single cell analysis. Reinvented.

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Again we have some exciting news to share with you. A new, groundbreaking method for single cell analysis based on FluidFM® technology allows scientist to investigate the behavior of individual cells in their natural environment. The new method was developed at ETH Zurich and could revolutionize biological research as it opens up a completely new dimension for the study of individual cells. The procedure makes it possible to sample the content of individual cells for molecular analyses directly in their native environment while preserving the entire cellular context. Consequently, it can be applied repeatedly to the same cell without destroying it in the process.


Biologists are more and more interested to study the behavior of individual cells within a population. Studying the properties and behavior of individual cell rather than the conduct of an entire cell population can thereby lead to a much deeper understanding of the underlying biological processes. The newly developed technique relies on the usage of a FluidFM nanosyringe in order to penetrate single living cells and extract their content for further investigation. The subsequent downstream analysis of the collected samples can then be carried out using well established procedures. This way scientists can discover subtle differences between individual cells within a population at a molecular level. The method can therefore also be applied to discover and investigate very rare cell types. “Our method opens up new frontiers in biological research. It is the start of a whole new chapter, so to speak”, says Professor Julia Vorholt from the Department of Biology at ETH Zurich who is leading the research group that developed the new method.


Compared to existing methods, the newly developed technique has numerous advantages: Thanks to the unique properties of the underlying FluidFM technology, researchers can sample individual cells within a tissue culture directly within their native environment. The method can thereby be repeatedly applied to the same cell. In contrast to established methods for molecular analysis, FluidFM based single cell extraction does not require the cells under investigation to be separated and physically removed from their native environment. Furthermore, the cells are not destroyed in the process and can thereby be repeatedly sampled in order to study them over longer time periods. “This means we can study how a cell affects its neighboring cells” explains Dr. Orane Guillaume-Gentil who is a postdoc in Professor Vorholt’s research group. Thanks to the new FluidFM based extraction of single cells it is now possible to conduct single cell analysis studies while preserving the entire cellular context with respect to space and time.

Unprecedented precision

Thanks to the highly precise nature of the utilized FluidFM nanosyringe probe, scientist are even able to distinguish between extracting contents directly from the nucleus of a cell or from the surrounding cytosol. The extracted volume can thereby be directly quantified with extreme accuracy down to 0.1 picoliter (10e-13 l or one tenth of a trillionth of a liter). This way it is possible to extract only as much liquid as needed. The sampled cell remains alive and can therefore be tested repeatedly over time. The scientists at ETH Zurich have published their new method in the well renowned journal “Cell” by analyzing RNA and protein activity of individual cells. For the future they plan to expand the portfolio of compatible downstream analysis methods in order to investigate also metabolites at the single cell level.

FluidFM as a platform technology

The newly developed method is based entirely on FluidFM technology. This technique has initially been developed at ETH Zurich and has since seen further expansion in its application portfolio over the years. The technique is being commercialized by the ETH Zurich spin-off company Cytosurge. While it was already possible to inject and isolate individual cells using FluidFM technology, this newly developed method adds another chapter in the application scope of FluidFM technology.


The amount of issues that needed to be solved goes well beyond simply extracting a cell and depositing the sample into some container. It was necessary to find new coating for FluidFM probes in order to prevent fouling by the extracted cellular contents. Furthermore, the utilized downstream analysis methods needed to be adapted in order to be compatible with the minute amounts of sample volumes that can be obtained from a single cell. This work has been carried out with the support of other research groups and individuals at ETH Zurich, namely Tomaso Zambelli, Privatdozent at ETH Zurich’s Department of Information Technology and Electrical Engineering and Martin Pilhofer, Professor at the Institute of Molecular Biology and Biophysics.


“Professor Vorholt and her research group really made a phenomenal effort by developing this new method for the extraction of individual cells” says Dr. Pascal Behr, CEO of Cytosurge. “This really brings an entirely new chapter to FluidFM and allows us to further strengthen our value proposition to our customers” Pascal Behr continues. “With the addition of this new single cell extraction method, FluidFM technology is really transforming into a true platform technology. We can now offer solutions ranging from biophysical investigations to micro 3D printing of metals as well as comprehensive single cell analysis.”

Sources 

Publication in Cell 
ETH news article 

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  • Prabhjot Kaur an Fr. 10.11.2017 08:09

    Various new techniques are developed in the environment to have a better pace with the technology. Also, this helps in time saving and gives better results while increasing the productivity of the work done. The new techniques even call for a great number of doubts by the students. So, in order to solves one’s queries, there is a website that enables you to submit your assignment with a minimal charge to be solved by the experts.

  • Alexander Serre an So. 24.09.2017 17:14

    Very good article!

    I look forward to the next one.

    Alex