Ulrike Kutay: "...biological science is most insightful when conducted in diverse teams..."

Ulrike Kutay will give the IUBMB Lecture at the at the 50th FEBS Congress (4–8 July 2026, Maastricht, The Netherlands). On this post she explores the top three research developments in her field and flags the necessary new skills of the modern molecular life scientist.
Ulrike Kutay: "...biological science is most insightful when conducted in diverse teams..."
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Portrait of Ulrike Kutay
Ulrike Kutay is a full professor of Biochemistry at the Department of Biology at the ETH in Zurich. She studied Biochemistry in Berlin, where she obtained her PhD on the integration of tail-anchored proteins into the ER membrane. During her postdoc in Heidelberg, she investigated the mechanisms governing nucleo-cytoplasmic transport. At the ETH in Zurich, Ulrike and her group explore the organization, function and dynamics of the human cell nucleus. Work of her team helped to unravel the mechanisms governing nuclear envelope breakdown for open mitosis, membrane protein targeting to the inner nuclear membrane, the biogenesis and organization of NE-spanning LINC complexes as well as the mechanisms driving the assembly of ribosomal subunits. Ulrike Kutay received an ERC Advanced Grant (2012), the ETH Zurich Alea Award (2020), the SNSF Advanced Grant (2022), and is an elected member of EMBO (2010), the Leopoldina (2012) and the Academy of Europe (2014). She has been Chair of the Institute of Biochemistry of ETH Zurich and served as the President of the ETH Zurich Strategy Committee.

What do you consider the most formative phase of your research career?

My undergraduate years were certainly the most formative phase of my career. Already then, I spent nearly every spare moment in research labs—starting at the East German Academy of Sciences in Berlin-Buch, where I later conducted my PhD studies after it had become the Max-Delbrück Center. During this period, I first fell in love with the 'bench' side of science. The hands-on nature of biochemical work and that initial spark of discovery really influenced my decision for a path as a researcher.

What do you see as the most important developments that have influenced the way you do research in the past 15 years?

Three developments were particularly transformative. First to mention is the introduction of CRISPR-Cas9 as a gene-editing tool. For our mechanistic work in mammalian cell biology, it has become an indispensable part of the toolkit for both gene inactivation and endogenous protein tagging. Second is the 'resolution revolution' in single-particle cryo-EM and cryo-tomography. In my view, seeing is believing; the high-resolution structures that are now obtainable are decisive for building accurate mechanistic models of cellular processes. Finally, there is AlphaFold, which I use almost daily. A decade ago, obtaining a reasonable structural model for a protein complex could take years of labour; today, we can generate testable predictions in minutes. I am incredibly eager to see how much this will accelerate the pace of drug discovery.

What comes first: technique or biological question?

For me, the biological question comes first, then the technology or method that enables us to find answers.

What do you consider to be the most important skills and areas of knowledge for molecular life scientists nowadays?

In the last century, many biochemists built their entire careers around studying a single protein from start to end, or mastering one specific, sophisticated method. Today, I believe that this level of specialization is no longer sufficient; one must be far more versatile.

From my perspective, for a modern molecular life scientist, computational literacy is essential. You must also be adept at interdisciplinary communication, working fluently at the intersections of chemistry, physics, and data science. Furthermore, you need the technical breadth to study molecular players across scales—from atomic structure to systemic physiology. Because of this complexity, I find that biological science is most insightful when conducted in diverse teams where different backgrounds come together to solve a problem.


Lab webpage:

https://bc.biol.ethz.ch/research/kutay.html

Two recent/key papers:

Lewis, R., Sinigiani, V., Maziak, N. et al. LBR and LAP2 mediate heterochromatin tethering to the nuclear periphery to preserve genome homeostasis. Nat Cell Biol (2026). https://doi.org/10.1038/s41556-025-01822-7

Maslennikova, D. et al. Dystonia-associated Torsins sustain CLCC1 function to promote membrane fusion of the nuclear envelope for NPC biogenesis. bioRxiv 2025.11.07.687155. https://doi.org/10.1101/2025.11.07.687155


More information on the IUBMB plenary lecture at the 50th FEBS Congress

Ulrike Kutay will give the IUBMB Lecture at the 50th FEBS Congress in Maastricht, the Netherlands on Saturday 4th July 2026 on 'The nuclear envelope – from genome organisation to nuclear pore complex biogenesis’.


Photo by Puscas Adryan on Unsplash.

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