PRESSEPORTAL Presseportal Logo
Alle Storys
Keine Story von Technische Universität München mehr verpassen.

17.03.2020 – 11:55

Technische Universität München

Artificial sugar-binding protein may inhibit cell growth


Corporate Communications Center

phone: +49 8161/ 71-5403 - e-mail: - web:

This text on the web:

High resolution images:


Artificial sugar-binding protein may inhibit cell growth

Blocking sugar structures on viruses and tumor cells

During a viral infection, viruses enter the body and multiply in its cells. Viruses often specifically attach themselves to the sugar structures of the host cells, or present characteristic sugar structures on their surface themselves. Researchers at the Technical University of Munich (TUM) have developed a new type of protein reagent for identifying biological sugar structures, which may block the spread of an illness in the body if used for blocking the sugar structures of a cell or a pathogen.

The laboratory directed by Arne Skerra, Professor of Biological Chemistry, has its focus on designing artificial binding proteins for therapeutic applications. The laboratory’s current research findings are paving the way for the development of new types of binding proteins for biological sugar structures, which play a significant role in cancer as well as infectious diseases.

Recognizing biological sugar structures

“The recognition of specific sugar molecules, or so-called carbohydrates, is of vital importance in many biological processes,” Prof. Skerra explains. Most cells carry a marker consisting of sugar chains which are attached to the outside of the cell membrane or to the membrane proteins, thus enabling the body to identify where these cells belong or whether certain cells are alien. Pathogens also have sugar structures of their own, or they can bind to these.

Proteins, which perform a wide range of functions within cells, generally have only low affinity to sugars. Thus, their molecular recognition poses a challenge. The reason: water molecules look similar to the sugar molecules, meaning that they are basically hidden in the aqueous environment of the cells. Prof. Skerra’s research group therefore set out to design an artificial binding protein with a peculiar chemical composition which makes it easier to bind to biological sugar structures.

A boric acid group implemented into a protein as amino acid

Amino acids are the building blocks of proteins. As a rule, nature only uses 20 amino acids in all living organisms. “Using the possibilities opened up by synthetic biology, we have employed an additional artificial amino acid,” reports researcher Carina A. Sommer.

“We have succeeded in incorporating a boric acid group, which exerts intrinsic affinity to sugar molecules, into the amino acid chain of a protein. In doing this, we have created an entirely new class of binding protein for sugar molecules,” Sommer explains. This artificial sugar-binding function is superior to natural binding proteins (so-called lectins) both in strength and with regard to possible sugar specificities.

“The sugar-binding activity of boric acid and its derivatives has been known for nearly a century,” says Prof. Skerra. “The chemical element boron is common on earth and has low toxicity, but so far has largely remained unexplored by organisms.”

“By using X-ray crystallography, we have succeeded in unraveling the crystal structure of a model complex of this artificial protein, which allowed us to validate our biomolecular concept,” explains scientist Dr. Andreas Eichinger.

The next step: towards medical application

Following approximately five years of fundamental scientific research, the findings from Prof. Skerra’s laboratory can now be applied to practical medical needs. Prof. Skerra points out: “Our results should not only be used to support the future development of new carbohydrate ligands in biological chemistry, but should also pave the way for creating high-affinity agents for controlling or blocking medically-relevant sugar structures on cell surfaces.”

Such a “blocking agent” could be used for conditions in which strong cell growth is evident or when pathogens are attaching themselves to cells, for example in oncology and virology. If we are successful in blocking the sugar-binding function and in slowing down the progress of a disease, this would give the patient’s immune system sufficient time to mobilize the body's natural defense.



Carina A. Sommer, Andreas Eichinger, and Arne Skerra (2020): A Tetrahedral Boronic Acid Diester Formed by an Unnatural Amino Acid in the Ligand Pocket of an Engineered Lipocalin. ChemBioChem 21:469-472. DOI: 10.1002/cbic.201900405

Images for journalists:


Prof. Dr. Arne Skerra

Technical University of Munich

Chair of Biological Chemistry

Tel.: +49 (0)8161 71-4351


The Technical University of Munich (TUM) is one of Europe’s leading research universities, with around 600 professors, 43,000 students, and 10,000 academic and non-academic staff. Its focus areas are the engineering sciences, natural sciences, life sciences and medicine, combined with economic and social sciences. TUM acts as an entrepreneurial university that promotes talents and creates value for society. In that it profits from having strong partners in science and industry. It is represented worldwide with the TUM Asia campus in Singapore as well as offices in Beijing, Brussels, Cairo, Mumbai, San Francisco, and São Paulo. Nobel Prize winners and inventors such as Rudolf Diesel, Carl von Linde, and Rudolf Mößbauer have done research at TUM. In 2006, 2012, and 2019 it won recognition as a German "Excellence University." In international rankings, TUM regularly places among the best universities in Germany.

Weitere Storys: Technische Universität München
Weitere Storys: Technische Universität München