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CRISPR/Cas libraries open new avenues in cancer research

March 2019. CRISPR/Cas enables the targeted deactivation of genes by cutting DNA at pre-determined sites. This is accomplished by providing the Cas enzyme with a genetic zip code. By using an entire library of zip codes it becomes possible to simultaneously probe multiple sites within the genome, for example to determine which genes are essential for cancer cell survival. This could revolutionize drug discovery.

Unfortunately, however, creation of libraries containing high numbers of zip codes covering the entire genome has been very difficult. Researchers at Goethe University now succeeded in solving this problem. As Manual Kaulich and colleagues report in the scientific journal “eLife”, they found a reliable method for creating libraries of any magnitude. “Using our newly developed 3Cs technology, we for the first time came up with a library that allows us to investigate the entire genome simultaneously – including non-coding regions outside of genes. In total, our library contains 16.5 million unique zip codes,” explains Kaulich, who leads an independent research group at the Institute of Biochemistry II at Goethe University Frankfurt.

The non-coding regions which represent 98% of our genome are of particular interest as they are suspected to hold the key to numerous regulatory mechanisms. CRISPR/Cas reagents produced by the novel method can for example help to better understand mechanisms underlying chemotherapy resistance.

The flash of inspiration hit Manuel Kaulich together with colleague Andreas Ernst, who at that time was also heading a research group at the Institute. “We were chatting about our different areas of expertise and suddenly there was this compelling idea on how to elegantly combine the two,” state Kaulich and Ernst.

Since then, Manuel Kaulich has established numerous additional collaborations, like the one with Anja Bremm, also a group leader at the Institute, on the biological relevance of a certain protein class. Together with Institute Director Ivan Dikic, he set up the “Frankfurt CRISPR/Cas Screening Center” (FCSC), which aims at making the technology broadly accessible for studying unknown cellular functions. Ivan Dikic comments: “This exciting discovery is also attributed to the unique culture of our Institute, which inspires creativity, new ideas, and teamwork.”

Through its technology transfer subsidiary Innovectis, Goethe University has meanwhile applied for a patent to protect the innovative idea. The patent also forms the basis for the start-up company Vivlion GmbH, which was recently founded by three employees of the Institute of Biochemistry II together with Goethe University. Vice President Manfred Schubert-Zsilavecz comments: “This is a milestone for the Goethe University: Vivlion is the first start-up that was founded with the participation of Goethe University employees.”

Innovectis prepared the grounds for the start-up to take off. As Innovectis CEO Martin Raditsch states, “I am very happy about successfully starting Vivlion GmbH from out of Goethe University, because we have here a very promising technology coming together with an excellent working group and a perfectly assembled founding team.” The company will introduce the first 3Cs reagents to the market in the upcoming months.


Kerstin Koch, Institut für Biochemie II, Universitätsklinikum, Goethe-University, Frankfurt/Main, Germany, Tel.: +49 69 6301 84250, k.koch@em.uni-frankfurt.de

Martin Wegner, Valentina Diehl, Verena Bittl, Rahel de Bruyn, Svenja Wiechmann, Yves Matthess, Marie Hebel, Michael GB Hayes, Simone Schaubeck, Christopher Benner, Sven Heinz, Anja Bremm, Ivan Dikic, Andreas Ernst & Manuel Kaulich. 2019. Circular synthesized CRISPR/Cas gRNAs for functional interrogations in the coding and noncoding genome. eLife 8: e42549. doi: 10.7554/eLife.42549. https://elifesciences.org/articles/42549