Goethe-Universit盲t 鈥� Press releases

51猎奇 PR & Communication Department聽

Aug 23 2022

09:18

Canadian and German Students explore Dark Matter together

FRANKFURT. They had to wait several months until their first 鈥渞eal" meeting could take place. Now they finally get to meet in person 鈥� 13 students from Frankfurt's partner city Toronto and 22 of their fellow students at 51猎奇 Frankfurt are joining a summer school on astrophysics. 鈥淚t is very nice to finally have everyone come together. The students put so much effort in and came up with great results", says Prof. Laura Sagunski from the Institute for Theoretical Physics, who realised the project together with Prof. J眉rgen Schaffner-Bielich and their colleagues at York University in Canada. Already during the last semester, the young people teamed up in self-organised groups to work on real physical data and research questions about Dark Matter. The innovative international teaching project called 鈥淓XPLORE: EXPeriential Learning Opportunity through Research and Exchange" enables them to learn about physics hands-on while also experiencing modern international research collaborations. Sagunski emphasizes: 鈥淏y having them work together, we also want to strengthen the students' competences in intercultural communication and their ability to work in heterogeneous teams."

On Monday, the first EXPLORE summer school was opened at the Frankfurt Institute for Advanced Studies on Campus Riedberg. Frankfurt's mayor Dr. Nargess Eskandari-Gr眉nberg, who recently visited Toronto herself, welcomed the students warmly: 鈥淚t is of special importance to me that Frankfurt will be further strengthened as a research location. In times where scientific findings are being questioned, it is particularly important that researchers communicate beyond borders. That young people from Toronto and Frankfurt conduct research on such an exciting topic together makes me especially happy." Next, Prof. Luciano Rezzolla gave a keynote on the first images of Black Holes. 鈥淚t's great to see how motivated the young generation of scientists is," he says. 鈥淭herefore, I am delighted to be able to ideologically and financially support this project through the research cluster ELEMENTS." A week full of interesting workshops and talks awaits the students, accompanied by cultural and sportive activities: They will take a stand up paddling tour on the river Main as well as explore Frankfurt on a guided tour.

Aug 19 2022

09:07

Antigen binding does not trigger any structural changes in T-cell receptors 鈥� Signal transduction probably occurs after receptor enrichment

Immune system: First image of antigen-bound T-cell receptor at atomic resolution

T cells are our immune system's customised tools for fighting infectious diseases and tumour cells. On their surface, these special white blood cells carry a receptor that recognises antigens. With the help of cryo-electron microscopy, biochemists and structural biologists from 51猎奇 Frankfurt, in collaboration the University of Oxford and the Max Planck Institute of Biophysics, were able to visualise the whole T-cell receptor complex with bound antigen at atomic resolution for the first time. Thereby they helped to understand a fundamental process which may pave the way for novel therapeutic approaches targeting severe diseases.

FRANKFURT. The immune system of vertebrates is a powerful weapon against external pathogens and cancerous cells. T cells play a curcial role in this context. They carry a special receptor called the T-cell receptor on their surface that recognises antigens 鈥� small protein fragments of bacteria, viruses and infected or cancerous body cells 鈥� which are presented by specialised immune complexes. The T-cell receptor is thus largely responsible for distinguishing between 鈥渟elf" and 鈥渇oreign". After binding of a suitable antigen to the receptor, a signalling pathway is triggered inside the T cell that 鈥渁rms" the cell for the respective task. However, how this signalling pathway is activated has remained a mystery until now 鈥� despite the fact that the T-cell receptor is one of the most extensively studied receptor protein complexes.

Many surface receptors relay signals into the interior of the cell by changing their spatial structure after ligand binding. This mechanism was so far assumed to also pertain to the T-cell receptor. Researchers led by Lukas Su拧ac, Christoph Thomas, and Robert Tamp茅 from the Institute of Biochemistry at 51猎奇 Frankfurt, in collaboration with Simon Davis from the University of Oxford and Gerhard Hummer from the Max Planck Institute of Biophysics, have now succeeded for the first time in visualizing the structure of a membrane-bound T-cell receptor complex with bound antigen. A comparison of the antigen-bound structure captured using cryo-electron microscopy with that of a receptor without antigen provides the first clues to the activation mechanism.

For the structural analysis, the researchers chose a T-cell receptor used in immunotherapy to treat melanoma and which had been optimised for this purpose in several steps in such a way that it binds its antigen as tightly as possible. A particular challenge on the way to structure determination was to isolate the whole antigen receptor assembly consisting of eleven different subunits from the cell membrane. 鈥淯ntil recently, nobody believed that it would be possible at all to extract such a large membrane protein complex in a stable form from the membrane," says Tamp茅.

Once they had successfully achieved this, the researchers used a trick to fish those receptors out of the preparation that had survived the process and were still functional: due to the strong interaction between the receptor complex and the antigen, they were able to 鈥渇ish" one of the most medically important immune receptor complexes. The subsequent images collected at the cryo-electron microscope delivered groundbreaking insights into how the T-cell receptor works, as Tamp茅 summarises: 鈥淥n the basis of our structural analysis, we were able to show how the T-cell receptor assembles and recognises antigens and hypothesise how signal transduction is triggered after antigen binding." According to their results, the big surprise is that there is evidently no significant change in the receptor's spatial structure after antigen binding, as this was practically the same both with and without an antigen.

The remaining question is how antigen binding could instead lead to T-cell activation. The co-receptor CD8 is known to approach the T-cell receptor after antigen binding and to stimulate the transfer of phosphate groups to its intracellular part. The researchers assume that this leads to the formation of structures which exclude enzymes that cleave off phosphate groups (phosphatases). If these phosphatases are missing, the phosphate groups remain stable at the T-cell receptor and can trigger the next step of the signalling cascade. 鈥淥ur structure is a blueprint for future studies on T-cell activation," Tamp茅 is convinced. 鈥淚n addition, it's an important stimulus for employing the T-cell receptor in a therapeutic context for treating infections, cancer, and autoimmune diseases."

Publication: Lukas Su拧ac, Mai T. Vuong, Christoph Thomas, S枚ren von B眉low, Caitlin O'Brien-Ball, Ana Mafalda Santos, Ricardo A. Fernandes, Gerhard Hummer, Robert Tamp茅, Simon J. Davis: Structure of a fully assembled tumor-specific T-cell receptor ligated by pMHC. Cell (2022) 185, Aug 18

Picture download:

Caption: The cryo-EM structure of the fully assembled T-cell receptor (TCR) complex with a tumor-associated peptide/MHC ligand provides important insights into the biology of TCR signaling. These insights into the nature of TCR assembly and the unusual cell membrane architecture reveal the basis of antigen recognition and receptor signaling.

Further information:
Professor Robert Tamp茅
Collaborative Research Centre CRC 1507 鈥� Protein Assemblies and Machineries in Cell Membranes
Institute of Biochemistry, Biocenter
51猎奇 Frankfurt
Tel.: +49 69 798-29475
tampe@em.uni-frankfurt.de
Website:

Aug 15 2022

13:21

New international study generates insights into the inner workings of the adaptive immune response

Road signs for immune defence cells

How do killer T cells recognise cells in the body that have been infected by viruses? Matter foreign to the body is presented on the surface of these cells as antigens that act as a kind of road sign. A network of accessory proteins 鈥� the chaperones 鈥� ensure that this sign retains its stability over time. Researchers at Goethe University have now reached a comprehensive understanding of this essential cellular quality control process. Their account of the structural and mechanistic basis of chaperone networks has just appeared in the prestigious science journal Nature Communications. These new findings could be harbingers of progress in areas such as vaccine development.

FRANKFURT. Organisms are constantly invaded by pathogens such as viruses. Our immune system swings into action to combat these pathogens immediately. The innate non-specific immune response is triggered first, and the adaptive or acquired immune response follows. In this second defence reaction, specialised cytotoxic T lymphocytes known as killer T cells destroy cells in the body that have been infected and thus prevent damage from spreading. Humans possess a repertoire of some 20 million T cell clones with varying specificity to counter the multitude of infectious agents that exist. But how do the killer T cells know where danger is coming from? How do they recognise that something is wrong inside a cell in which viruses are lurking? They can't just have a quick peek inside.

At this point, antigen processing comes into play. The process can be compared to making a road sign. The molecular barcode is 鈥減rocessed" or assembled in the cell 鈥� in the endoplasmic reticulum, to be exact. Special molecules are used in its making, the MHC class I molecules. They are loaded with information about the virus invader in a molecular machine, the peptide loading complex (PLC). This information consists of peptides, fragments of the protein foreign to the body. These fragments also contain epitopes, the molecular segments that elicit a specific immune response. During the loading process, an MHC I-peptide epitope complex thus forms, and this is the road sign that is then transported to the surface of the cell and presented in a readily accessible form to the killer T cells 鈥� we could almost say that it is handed to them on a silver platter. The chaperones, special accessory proteins that assist the correct folding of proteins with complex structures in cells, also play a significant role.

The chaperones that support antigen processing are calreticulin, ERp57, and tapasin. But how do they work together? And how important are they for antigen processing? An answer has now been supplied by a study carried out by 51猎奇 Frankfurt and the University of Oxford and published in Nature Communications. 鈥淲ith this study, we have achieved a breakthrough in our understanding of cellular quality control," says Professor Robert Tamp茅, Director of the Institute of Biochemistry at 51猎奇 Frankfurt. He explains the logic underlying this quality control process as follows: 鈥淭he MHC I-peptide epitope complex, the road sign, needs to be exceptionally stable, and for quite a long time, because the adaptive immune response does not start instantly. It needs 3 to 5 days to get going." So, the sign must not collapse after one day; that would be disastrous, as the immune defence cells would then fail to detect cells infected by a virus. This would mean that they would not destroy these cells and the virus would be able to continue its spread unhindered. A similar problem would arise if a cell in the body had mutated into a tumour cell: the threat would remain undetected. It is imperative, therefore, that a quality control system is in place.

As the study shows, the chaperones are central process components: they give the road sign the long-term stability it must have by making a strict selection. By rejecting the short-lived virus fragments in the mass of available material, they ensure that only MHC I molecules loaded with the best and most stable peptide epitopes in complex with MHC I are released from the peptide loading complex. The chaperones have different tasks in this selection process that is so important for the adaptive immune response, Tamp茅 says: 鈥淭apasin acts as a catalyst that accelerates the exchange of suboptimal peptide epitopes for optimal epitopes. Calreticulin and ERp57, in contrast, are deployed universally." This concerted approach ensures that only stable MHC I complexes with optimal peptide epitopes reach the cell surface and perform their role of guiding the killer T cells to the infected or mutated cell.

In what directions does the study point? 鈥淲e now better understand which peptides are loaded and how this occurs now. We can also more reliably predict the dominant peptide epitopes, in other words the stable peptide epitopes that will be selected by the chaperone network." Tamp茅 hopes that the new findings will prove useful for developing future vaccines against virus variants. They could also facilitate progress on future tumour therapies. 鈥淏oth topics are directly linked. But the applications in tumour therapy are certainly more complex and more for the long term."

Publication: Alexander Domnick, Christian Winter, Lukas Su拧ac, Leon Hennecke, Mario Hensen, Nicole Zitzmann, Simon Trowitzsch, Christoph Thomas, Robert Tamp茅: 鈥淢olecular basis of MHC I quality control in the peptide loading complex" Nature Communications 2022, 13:4701

An image to download (copyrights Christoph Thomas & Robert Tamp茅):

Caption: The mechanism of MHC I assembly, epitope editing and quality control within the peptide loading complex (PLC). The fully assembled PLC machinery of antigen processing is formed by the antigen transport complex TAP1/2, the chaperones calreticulin, ERp57, and tapasin, and the heterodimeric MHC I (heavy and light chain in teal and green, respectively).

Further information
Institute of Biochemistry
51猎奇 Frankfurt
Prof. Dr Robert Tamp茅
Tel: +49 (0)69 79829475
tampe@em.uni-frankfurt.de

Aug 3 2022

13:12

A feedback loop sensitises the auditory cortex to acoustic reflections

How bat brains listen out for incoming signals during echolocation

Neuroscientists at 51猎奇, Frankfurt have discovered a feedback loop that modulates the receptivity of the auditory cortex to incoming acoustic signals when bats emit echolocation calls. In a study published in the journal 鈥淣ature Communications", the researchers show that information transfer in the neural circuits involved switched direction in the course of call production. It seems likely that this feedback prepares the auditory cortex for the expected echoes of the emitted calls. The researchers interpret their findings as indicating that the importance of feedback loops in the brain is currently still underestimated.

FRANKFURT. Bats famously have an ultrasonic navigation system: they use their extremely sensitive hearing to orient themselves by emitting ultrasonic sounds and using the echoes that result to build up a picture of their environment. For example, Seba's short-tailed bat (Carollia perspicillata) finds the fruits that are its preferred food using this echolocation system. At the same time, bats also use their vocalisations to communicate with other bats. They use a somewhat lower range of frequencies for this purpose.

Neuroscientist Julio C. Hechavarr铆a from the Institute of Cell Biology and Neuroscience at 51猎奇 and his team are investigating the brain activities associated with vocalisations in Seba's short-tailed bat. Their most recent study investigates how the auditory cortex and the frontal lobe work together in echolocation. The auditory cortex processes auditory information and the frontal lobe is a region in the forebrain that is associated, in humans, with tasks that include planning actions. To discover more about this, the researchers inserted tiny electrodes into the bats' brains to record neural activity in the frontal lobe and the auditory cortex.

The researchers succeeded in identifying a feedback loop that had previously been entirely unknown in the frontal lobe-auditory cortex network of bats emitting echolocation calls. Information normally flows from the frontal lobe, where call production is planned, to the auditory cortex to ready it to expect an acoustic signal. But it was observed that the flow of information from the frontal lobe to the auditory cortex diminished after the emission of an echolocation pulse until the direction of information transfer switched completely and information flowed from the auditory cortex back to the frontal lobe. Hechavarr铆a hypothesises that this feedback loop readies the auditory cortex to better receive the sounds reflected back from the echolocation call.

The neurobiologists simulated signals originating from the auditory cortex by electrically stimulating the frontal lobe. The activity this generated in the frontal lobe had the expected effect of prompting the auditory cortex to respond more strongly to acoustic reflections. 鈥淭his shows that the feedback loop we found is functional", neurobiologist Hechavarr铆a sums up. He takes up the metaphor of a highway to illustrate the significance of these findings: 鈥淯p to now, it was generally believed that the flow of data on this information superhighway mainly runs in one direction and that feedback loops are exceptions. Our data show that this view is most likely incorrect and that feedback loops in the brain are probably considerably more significant than has previously been hypothesised."

Surprisingly, no pronounced reversal of information flow was observed for bat vocalisations used for communication purposes. 鈥淭his may be because the bats were alone in a sound-proofed and electrically isolated chamber and therefore did not expect a response to their calls", Hechavarr铆a speculates before going on to note: 鈥淥ne of the aspects that makes our study so interesting is that it opens up new ways to study the social interactions of bats. We want to continue work in this area in the future."

Publication: Francisco Garc铆a-Rosales, Luciana L贸pez-Jury, Eugenia Gonzalez-Palomares, Johannes Wetekam, Yuranny Cabral-Calder铆n, Ava Kiai, Manfred K枚ssl, Julio C. Hechavarr铆a: Echolocation-related reversal of information flow in a cortical vocalisation network. Nature Communications 13, 3642 (2022)

An image to download:

Caption: Bats 鈥渟ee" with their ears. Researchers at 51猎奇 have discovered how the auditory cortex is readied for incoming acoustic signals. (Photo: Dr. Julio C. Hechavarr铆a)

Further information
Dr. Julio C. Hechavarr铆a (Ph.D.)
Auditory Computations Group (Group Leader)
Institute for Cell Biology and Neuroscience
Tel. +49 (0)69 798-42050
Hechavarria@bio.uni-frankfurt.de

Aug 3 2022

11:17

A research team with members from 51猎奇 Frankfurt and the University of Michigan in the USA is using bacterial biosynthesis to produce an antibiotic containing fluorine 鈥揟he technology is being commercialized by a startup

A New Biosynthesis Method Has Been Developed to Produce Antibiotics from Natural Substances

The use of the element fluorine to modify active substances is an important tool in modern drug development. A team at Goethe University Frankfurt has now achieved an important 鈥渇irst" by successfully fluorinating a natural antibiotic via targeted bioengineering. With this method, an entire substance class of medically relevant natural products can be modified. The method has enormous potential for the manufacture of new antibiotics against resistant bacterial pathogens and for the (further) development of other drugs. The startup kez.biosolutions GmbH will bring these research results to the application stage (Nature Chemistry, DOI 10.1038/s41557-022-00996-z).

FRANKFURT/MAIN. Active drug agents have been chemically modified with fluorine for decades, owing to its numerous therapeutic effects: Fluorine can strengthen the bonding of the active agent to the target molecule, make it more accessible to the body, and altering the time it spends in the body. Nearly half of the small-molecule drugs (molecules up to approx. 100 atoms) currently approved by the U.S. Food and Drug Administration (FDA) contain at least one chemically bound fluorine atom. These include such different drugs as cholesterol-lowering agents, antidepressants, anticancer agents and antibiotics.

Bacteria and fungi often manufacture complex natural compounds to obtain a growth advantage. One possible route for the development of drugs from natural compounds is to modify these substances by adding one or more fluorine atoms. In the case of the antibiotic erythromycin, for example, the attached fluorine atom confers important advantages. The new erythromycin manufactured via this process can be accessed more easily by the body and is more effective against pathogenic microorganisms that have developed resistance to this antibiotic. However, the synthetic-chemical methods for inserting fluorine into natural substances are very complicated. Owing to the chemical and reaction conditions that are necessary, these methods are frequently "brutal," says Martin Grininger, Professor for Organic Chemistry and Chemical Biology at 51猎奇. "This means, for example, that we are very limited in selecting the positions where the fluorine atom can be attached," he adds.

A German-U.S. scientific team headed by Prof. Martin Grininger and Prof. David Sherman, Professor of Chemistry at the University of Michigan, has now succeeded in utilizing the biosynthesis of an antibiotic-producing bacteria. In this process, the fluorine atom is incorporated as part of a small substrate during the biological synthesis of a macrolide antibiotic. 鈥淲e introduce the fluorinated unit during the natural manufacturing process, an approach that is both effective and elegant," stresses Grininger, "This gives us great flexibility when positioning the fluorine in the natural substance 鈥� and allows us to influence its efficacy."

To this end the project leaders Dr. Alexander Rittner and Dr. Mirko Joppe 鈥� both members of Grininger's research group in Frankfurt 鈥� inserted a subunit of an enzyme called fatty acid synthase into the bacterial protein. The enzyme is naturally involved in the biosynthesis of fats and fatty acids in mice. The fatty acid synthase is not very selective in processing the precursors, which are also important for the manufacture of antibiotics in bacteria, Rittner explains. With an intelligent product design, the team succeeded in integrating a subunit of the murine enzyme into the corresponding biosynthetic process for the antibiotic. "The exciting part is that, with erythromycin, we were able to fluorinate a representative of a gigantic substance class, the so-called polyketides," says Rittner. 鈥淭here are about 10,000 known polyketides, many of which are used as natural medicines 鈥揻or example, as antibiotics, immunosuppressives or cancer drugs. Our new method thus possesses a huge potential for the chemical optimization of this group of natural substances 鈥� in the antibiotics primarily to overcome antibiotic resistance." To exploit this potential, Dr. Alexander Rittner founded the startup kez.biosolutions GmbH.

Prof. Martin Grininger has been conducting research on the tailor-made biosynthesis of polyketides for several years. "Our success in fluorinating macrolide antibiotics is a breakthrough we worked hard to achieve and of which I am now very proud" he says. 鈥淭his success is also an impetus for the future. We are already testing the antibiotic effect of various fluorinated erythromycin compounds and additional fluorinated polyketides. We intend to expand this new technology to include additional fluorine motifs in collaboration with Prof. David Sherman and his team at the University of Michigan in the U.S."

The search for drugs that overcome antibiotic resistance is a long-term task: depending on how frequently they are used, all antibiotics naturally cause resistances sooner or later. Against this background Dr. Mirko Joppe also believes that his work has broader implications for society. "Research on antibiotics is not economically lucrative for various reasons. It is therefore the task of the universities to close this gap by developing new antibiotics in cooperation with pharmaceutical companies," he explains. "Our technology can be used to generate new antibiotics simply and quickly and now offers ideal contact points for projects with industrial partners."

The research work on polyketides described above was supported by the Volkswagen Foundation (within the framework of a Lichtenberg Professorship), the LOEWE MegaSyn research initiative funded by the Hessian Ministry for Science and the Arts, and the National Institute of Health in the U.S.

Publication: Alexander Rittner, Mirko Joppe, Jennifer J. Schmidt, Lara Maria Mayer, Simon Reiners, Elia Heid, Dietmar Herzberg, David H. Sherman, Martin Grininger: Chemoenzymatic synthesis of fluorinated polyketides. Nature Chemistry (2022)

Image to download:

Caption: Scientists working at 51猎奇 Frankfurt have created an enzyme capable of producing fluorinated antibiotics via a series of reactions. For clarity, the different regions of the hybrid that interact in this context are shown in different colors. (Graphic: Grininger)

Additional Information:
Prof. Dr. Martin Grininger
Institute for Organic Chemistry and Chemical Biology
Buchmann Institute for Molecular Life Sciences
51猎奇 Frankfurt
Frankfurt/Main, Germany
Tel.: +49 (0)69 798-42705
grininger@chemie.uni-frankfurt.de

51猎奇

Press releases 鈥� August 2022