Publications

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Articles

Puravankara Menon, A., Villanueva, H., Meraviglia-Crivelli, D. H., van Santen, H. M., Hellmeier, J., Zheleva, A., Nonateli, F., Peters, T., Wachsmann, T. L. A., Hernandez-Rueda, M., Huppa, J. B., Schütz, G., Sevcsik, E., Moreno, B., & Pastor, F. (2024). CD3 aptamers promote expansion and persistence of tumor-reactive T cells for adoptive T cell therapy in cancer. MOLECULAR THERAPY NUCLEIC ACIDS, 35(2), Article 102198. https://doi.org/10.1016/j.omtn.2024.102198
| CD3 aptamers promote expansion and persistence of tumor-reactive T cells for adoptive T cell therapy in cancer at reposiTUm , opens an external URL in a new window
Moura, S., Hartl, I., Brumovska, V., Calabrese, P. P., Yasari, A., Striedner, Y., Bishara, M., Mair, T., Ebner, T., Schütz, G., Sevcsik, E., & Tiemann-Boege, I. (2024). Exploring FGFR3 mutations in the male germline: implications for clonal germline expansions and paternal age-related dysplasias. Genome Biology and Evolution, 16(2), Article evae015. https://doi.org/10.1093/gbe/evae015
| Exploring FGFR3 mutations in the male germline: implications for clonal germline expansions and paternal age-related dysplasias at reposiTUm , opens an external URL in a new window
Hartl, I., Brumovska, V., Striedner, Y., Yasari, A., Schütz, G., Sevcsik, E., & Tiemann-Boege, I. (2023). Measurement of FGFR3 signaling at the cell membrane via total internal reflection fluorescence microscopy to compare the activation of FGFR3 mutants. Journal of Biological Chemistry, 299(2), Article 102832. https://doi.org/10.1016/j.jbc.2022.102832
| Measurement of FGFR3 signaling at the cell membrane via total internal reflection fluorescence microscopy to compare the activation of FGFR3 mutants at reposiTUm , opens an external URL in a new window
Platzer, R., Hellmeier, J., Göhring, J., Perez, I. D., Schatzlmaier, P., Bodner, C., Focke-Tejkl, M., Schütz, G. J., Sevcsik, E., Stockinger, H., Brameshuber, M., & Huppa, J. B. (2023). Monomeric agonist peptide/MHCII complexes activate T-cells in an autonomous fashion. EMBO Reports, Article e57842. https://doi.org/10.15252/embr.202357842
| Monomeric agonist peptide/MHCII complexes activate T-cells in an autonomous fashion at reposiTUm , opens an external URL in a new window
Hellmeier, J., Platzer, R., Eklund, A. S., Schlichthaerle, T., Karner, A., Motsch, V., Schneider, M. C., Kurz, E., Bamieh, V., Brameshuber, M., Preiner, J., Jungmann, R., Stockinger, H., Schütz, G. J., Huppa, J. B., & Sevcsik, E. (2021). DNA origami demonstrate the unique stimulatory power of single pMHCs as T cell antigens. Proceedings of the National Academy of Sciences, 118(4). https://doi.org/10.1073/pnas.2016857118
| DNA origami demonstrate the unique stimulatory power of single pMHCs as T cell antigens at reposiTUm , opens an external URL in a new window
Hellmeier, J., Platzer, R., Mühlgrabner, V., Schneider, M. C., Kurz, E., Schütz, G. J., Huppa, J. B., & Sevcsik, E. (2021). Strategies for the Site-Specific Decoration of DNA Origami Nanostructures with Functionally Intact Proteins. ACS Nano, 15(9), 15057–15068. https://doi.org/10.1021/acsnano.1c05411
| Strategies for the Site-Specific Decoration of DNA Origami Nanostructures with Functionally Intact Proteins at reposiTUm , opens an external URL in a new window
Schromm, A. B., Paulowski, L., Kaconis, Y., Kopp, F., Koistinen, M., Donoghue, A., Keese, S., Nehls, C., Wernecke, J., Garidel, P., Sevcsik, E., Lohner, K., Sanchez-Gomez, S., Martinez-de-Tejada, G., Brandenburg, K., Brameshuber, M., Schütz, G. J., Andrä, J., & Gutsmann, T. (2021). Cathelicidin and PMB neutralize endotoxins by multifactorial mechanisms including LPS interaction and targeting of host cell membranes. Proceedings of the National Academy of Sciences, 118(27). https://doi.org/10.1073/pnas.2101721118
| Cathelicidin and PMB neutralize endotoxins by multifactorial mechanisms including LPS interaction and targeting of host cell membranes at reposiTUm , opens an external URL in a new window
Arnold, A. M., Reismann, A. W. A. F., Sevcsik, E., & Schütz, G. J. (2020). Monte Carlo simulations of protein micropatterning in biomembranes: effects of immobile nanofeatures with reduced diffusivity. Journal of Physics D: Applied Physics, 53(43), 435401. https://doi.org/10.1088/1361-6463/aba297
| Monte Carlo simulations of protein micropatterning in biomembranes: effects of immobile nanofeatures with reduced diffusivity at reposiTUm , opens an external URL in a new window
Platzer, R., Rossboth, B. K., Schneider, M. C., Sevcsik, E., Baumgart, F., Stockinger, H., Schütz, G. J., Huppa, J. B., & Brameshuber, M. (2020). Unscrambling fluorophore blinking for comprehensive cluster detection via photoactivated localization microscopy. Nature Communications, 11(4993). https://doi.org/10.1038/s41467-020-18726-9
| Unscrambling fluorophore blinking for comprehensive cluster detection via photoactivated localization microscopy at reposiTUm , opens an external URL in a new window
Varadi, T. E., Schneider, M., Sevcsik, E., Kiesenhofer, D., Baumgart, F., Batta, G., Kovács, T., Platzer, R., Huppa, J. B., Szöllősi, J., Schütz, G., Brameshuber, M., & Nagy, P. (2019). Homo- and Heteroassociations Drive Activation of ErbB3. Biophysical Journal, 117(10), 1935–1947. https://doi.org/10.1016/j.bpj.2019.10.001
| Homo- and Heteroassociations Drive Activation of ErbB3 at reposiTUm , opens an external URL in a new window
Lindner, M., Tresztenyak, A., Fülöp, G., Jahr, W., Prinz, A., Prinz, I., Danzl, J. G., Schütz, G. J., & Sevcsik, E. (2019). A Fast and Simple Contact Printing Approach to Generate 2D Protein Nanopatterns. Frontiers in Chemistry, 6. https://doi.org/10.3389/fchem.2018.00655
| A Fast and Simple Contact Printing Approach to Generate 2D Protein Nanopatterns at reposiTUm , opens an external URL in a new window
Motsch, V., Brameshuber, M., Baumgart, F., Schütz, G. J., & Sevcsik, E. (2019). A micropatterning platform for quantifying interaction kinetics between the T cell receptor and an intracellular binding protein. Scientific Reports, 9(3288). https://doi.org/10.1038/s41598-019-39865-0
| A micropatterning platform for quantifying interaction kinetics between the T cell receptor and an intracellular binding protein at reposiTUm , opens an external URL in a new window
Brameshuber, M., Kellner, F., Rossboth, B., Ta, H., Alge, K., Sevcsik, E., Göhring, J., Axmann, M., Baumgart, F., Gascoigne, N. R. J., Darvis, S. J., Stockinger, H., Schütz, G., & Huppa, J. B. (2018). Monomeric TCRs Drive T Cell Antigen Recognition. Nature Immunology, 19(5), 487–496. https://doi.org/10.1038/s41590-018-0092-4
| Monomeric TCRs Drive T Cell Antigen Recognition at reposiTUm , opens an external URL in a new window
Fülöp, G., Brameshuber, M., Arnold, A., Schütz, G., & Sevcsik, E. (2018). Determination of the Membrane Environment of CD59 in Living Cells. Biomolecules, 8(2), Article 28. https://doi.org/10.3390/biom8020028
| Determination of the Membrane Environment of CD59 in Living Cells at reposiTUm , opens an external URL in a new window
Hager, R., Arnold, A., Sevcsik, E., Schütz, G. J., & Howorka, S. (2018). Tunable DNA Hybridization Enables Spatially and Temporally Controlled Surface-Anchoring of Biomolecular Cargo. Langmuir, 34(49), 15021–15027. https://doi.org/10.1021/acs.langmuir.8b01942
| Tunable DNA Hybridization Enables Spatially and Temporally Controlled Surface-Anchoring of Biomolecular Cargo at reposiTUm , opens an external URL in a new window
Schütz, G. J., Weghuber, J., Lanzerstorfer, P., & Sevcsik, E. (2017). Protein Micropatterning Assay: Quantitative Analysis of Protein-Protein Interactions. Methods in Molecular Biology, 261–270. https://doi.org/10.1007/978-1-4939-6747-6_18
| Protein Micropatterning Assay: Quantitative Analysis of Protein-Protein Interactions at reposiTUm , opens an external URL in a new window
Sevcsik, E., & Schütz, G. (2017). Proteins and lipids - a complicated relationship? ASBMB Today, 16(1), 9–10.
| Proteins and lipids - a complicated relationship? at reposiTUm , opens an external URL in a new window
Arnold, A. M., Sevcsik, E., & Schütz, G. J. (2016). Monte Carlo simulations of protein micropatterning in biomembranes: effects of immobile sticky obstacles. Journal of Physics D: Applied Physics, 49(36), 364002. https://doi.org/10.1088/0022-3727/49/36/364002
| Monte Carlo simulations of protein micropatterning in biomembranes: effects of immobile sticky obstacles at reposiTUm , opens an external URL in a new window
Brameshuber, M., Sevcsik, E., Rossboth, B. K., Manner, C., Deigner, H.-P., Peksel, B., Péter, M., Török, Z., Hermetter, A., & Schütz, G. J. (2016). Oxidized Phospholipids Inhibit the Formation of Cholesterol-Dependent Plasma Membrane Nanoplatforms. Biophysical Journal, 110(1), 205–213. https://doi.org/10.1016/j.bpj.2015.11.018
| Oxidized Phospholipids Inhibit the Formation of Cholesterol-Dependent Plasma Membrane Nanoplatforms at reposiTUm , opens an external URL in a new window
Sevcsik, E., & Schütz, G. J. (2016). With or without rafts? Alternative views on cell membranes. BioEssays, 38(2), 129–139. https://doi.org/10.1002/bies.201500150
| With or without rafts? Alternative views on cell membranes at reposiTUm , opens an external URL in a new window
Sevcsik, E., Brameshuber, M., Fölser, M., Weghuber, J., & Honigmann, A. (2015). GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane. Nature Communications, 6, 69691–696910.
| GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane at reposiTUm , opens an external URL in a new window

Books & Book Contributions

Hellmeier, J., Platzer, R., Huppa, J. B., & Sevcsik, E. (2023). A DNA Origami-Based Biointerface to Interrogate the Spatial Requirements for Sensitized T-Cell Antigen Recognition. In C. Baldari & M. L. Dustin (Eds.), The Immune Synapse. Methods and Protocols (Vol. 2654, pp. 277–302). Humana. https://doi.org/10.1007/978-1-0716-3135-5_18
| A DNA Origami-Based Biointerface to Interrogate the Spatial Requirements for Sensitized T-Cell Antigen Recognition at reposiTUm , opens an external URL in a new window

Inproceedings

Hellmeier, J., Platzer, R., Huppa, J., & Sevcsik, E. (2024). Spatial requirements for T-cell receptor triggering probed via a DNA origami-based biointerface. In 3rd MOSBRI Scientific Conference: 10th - 13th June 2024, Ljubljana, Slovenia: Programme Abstracts (pp. 77–77).
| Spatial requirements for T-cell receptor triggering probed via a DNA origami-based biointerface at reposiTUm , opens an external URL in a new window
Helfert, S., Hellmeier, J., Sevcsik, E., Liska, R., & Baudis, S. (2019). Tailor-made biointerfaces on oxidic substrates via polymer brushes. In Termis EU 2019 (p. 1338).
| Tailor-made biointerfaces on oxidic substrates via polymer brushes at reposiTUm , opens an external URL in a new window
Dobos, A., Gruber, P., Steiger, W., Fülöp, G., Sevcsik, E., Schütz, G., & Ovsianikov, A. (2018). High resolution 3D printing of biomimetic microenvironments to study T-cell activation. In G. Fülöp (Ed.), Abstract Book.
| High resolution 3D printing of biomimetic microenvironments to study T-cell activation at reposiTUm , opens an external URL in a new window
Helfert, S., Hellmeier, J., Sevcsik, E., Liska, R., & Baudis, S. (2018). Tailor-made Polymer Interfaces - Surfaces on Demand. In VSS 2018 (pp. 84–85). Book-of-Abstracts.com.
| Tailor-made Polymer Interfaces - Surfaces on Demand at reposiTUm , opens an external URL in a new window
Helfert, S., Dworak, C., Sevcsik, E., Peterlik, H., Ret, D., Sauer, M., & Liska, R. (2017). Synthesis and Characterization of Polymer Linker Systems for Cell Studies. In Bypos Workshop Book 2017 (p. 29).
| Synthesis and Characterization of Polymer Linker Systems for Cell Studies at reposiTUm , opens an external URL in a new window
Helfert, S., Dworak, C., Sevcsik, E., Peterlik, H., Sauer, M., Ret, D., & Liska, R. (2017). Design and Synthesis of Tailor-made Nanostructured Polymer Biointerfaces. In Danube Vltava Sava Polymer Meeting 2017 (p. OP-11). Book of Abstracts.com.
| Design and Synthesis of Tailor-made Nanostructured Polymer Biointerfaces at reposiTUm , opens an external URL in a new window
Helfert, S., Dworak, C., Sevcsik, E., Peterlik, H., Sauer, M., Ret, D., & Liska, R. (2017). Synthesis and Characterization of Polymer Linker systems for T-cell activation. In Advanced Polymers via Macromolecular Engineering (p. 133).
| Synthesis and Characterization of Polymer Linker systems for T-cell activation at reposiTUm , opens an external URL in a new window

Preprints

Hondl, N., Neubauer, L., Ramos Garcia, V., Kuligowski, J., Bishara, M., Sevcsik, E., Lendl, B., & Ramer, G. (2025). Chemical characterization of extracellular vesicles at the sub-vesicle level. ChemRxiv. https://doi.org/10.34726/8660
| Chemical characterization of extracellular vesicles at the sub-vesicle level at reposiTUm , opens an external URL in a new window

Talks

Sevcsik, E. (2024, June 2). Signaling from single TCRs? Dissecting binding kinetics and clustering in TCR-antigen recognition. Lymphocyte Antigen Receptor Signalling Workshop (2024), Siena, Italy.
| Signaling from single TCRs? Dissecting binding kinetics and clustering in TCR-antigen recognition at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2024, May 15). Spatial requirements for T-cell receptor triggering probed via a DNA origami-based biointerface. 20th International Life Science Meeting, Krems an der Donau, Austria.
| Spatial requirements for T-cell receptor triggering probed via a DNA origami-based biointerface at reposiTUm , opens an external URL in a new window
Majkova, A., Hellmeier, J., Platzer, R., Kopittke, C., Huppa, J., Schütz, G., & Sevcsik, E. (2023, December 1). Designing functionalized DNA origami-based biointerfaces for probing T-cell activation. Vienna Soft Matter Day, Wien, Austria.
| Designing functionalized DNA origami-based biointerfaces for probing T-cell activation at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2023, September 19). Spatial requirements for T-cell receptor triggering probed via a DNA origami-based biointerface. 2023 Fall Meeting of the European Materials Research Society (E-MRS), Warschau, Poland.
| Spatial requirements for T-cell receptor triggering probed via a DNA origami-based biointerface at reposiTUm , opens an external URL in a new window
Majkova, A., Hellmeier, J., Huppa, J. B., & Sevcsik, E. (2023, September 6). Designing functionalized DNA origami-based biointerfaces for probing cell-cell interaction. Active mechanics, from single cells to cell layers, tissues and development (SPLW02), Cambridge, United Kingdom of Great Britain and Northern Ireland (the).
| Designing functionalized DNA origami-based biointerfaces for probing cell-cell interaction at reposiTUm , opens an external URL in a new window
Majkova, A., Hellmeier, J., Platzer, R., Huppa, J., & Sevcsik, E. (2023, August 29). Designing functionalized DNA origami-based biointerfaces for probing T-cell activation. 12th Single Molecule Localization Microscopy Symposium (SMLMS) 2023, Wien, Austria.
| Designing functionalized DNA origami-based biointerfaces for probing T-cell activation at reposiTUm , opens an external URL in a new window
Bishara, M., Brumovska, V., Arnold, A. M., Kalouskova, B., Fülöp, G., Schütz, G., & Sevcsik, E. (2023, August 28). Protein micropatterning as a tool to probe the membrane environment of transmembrane proteins in live-cells. 12th Single Molecule Localization Microscopy Symposium (SMLMS) 2023, Wien, Austria.
| Protein micropatterning as a tool to probe the membrane environment of transmembrane proteins in live-cells at reposiTUm , opens an external URL in a new window
Brameshuber, E., Platzer, R., Rossboth, B., Sevcsik, E., Schneider, M., Schütz, G., & Huppa, J. B. (2023, August 28). Comprehensive Fluorophore Blinking Platform for Detecting Nanoscale Protein Distributions. 12th Single Molecule Localization Microscopy Symposium (SMLMS) 2023, Wien, Austria.
| Comprehensive Fluorophore Blinking Platform for Detecting Nanoscale Protein Distributions at reposiTUm , opens an external URL in a new window
Bishara, M., Brumovska, V., Arnold, A. M., Kalouskova, B., Fülöp, G., Schütz, G., & Sevcsik, E. (2023, August 2). Determining the nanoscopic membrane environment of transmembrane proteins in live-cells with protein micropatterning. European Biophysical Societies Association (EBSA Congress) 2023, Stockholm, Sweden.
| Determining the nanoscopic membrane environment of transmembrane proteins in live-cells with protein micropatterning at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2023, July 11). A DNA origami-based biointerface for interrogating the spatial requirements of T-cell antigen recognition. CellNanOS und SFB - Seminar, Osnabrück, Germany.
| A DNA origami-based biointerface for interrogating the spatial requirements of T-cell antigen recognition at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2023, April 13). Probing the spatial requirements for T-cell receptor triggering (invited talk). EMBO Workshop “ImmunoBiophysics: From fundamental physics to understanding the immune response,” Les Houches, France.
| Probing the spatial requirements for T-cell receptor triggering (invited talk) at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2023, January 10). Probing plasma membrane organization and function using microstructured biointerfaces. seminar series “Selected Topics in Membrane Biophysics,” Graz, Austria.
| Probing plasma membrane organization and function using microstructured biointerfaces at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2022, September 22). Distinct spatial requirements for TCR but not pMHC organization direct T-cell activation (talk). ÖGMBT Jahrestagung, Wien, Austria.
| Distinct spatial requirements for TCR but not pMHC organization direct T-cell activation (talk) at reposiTUm , opens an external URL in a new window
Bishara, M., Brumovska, V., Arnold, A. M., Fülöp, G., Schütz, G., & Sevcsik, E. (2022, September 11). Unraveling protein-lipid interactions in live-cells with protein micropatterning. Methods and Applications in Fluorescence, Göteborg, Sweden.
| Unraveling protein-lipid interactions in live-cells with protein micropatterning at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2022, September 7). A DNA origami-based biointerface for probing the spatial requirements of cell surface receptor triggering (Invited talk). 16th Multinational Congress on Microscopy, Brno, Czechia.
| A DNA origami-based biointerface for probing the spatial requirements of cell surface receptor triggering (Invited talk) at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2022, July 25). Micro- and nanostructured biointerfaces for studying cell surface receptor triggering. Membrane Symposium, Tulln/NÖ, Austria.
| Micro- and nanostructured biointerfaces for studying cell surface receptor triggering at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2022, July 10). Spatial requirements for T-cell receptor triggering probed via a DNA origami-based biointerface. Meeting of the Austrian Biophysical Society, Strobl/Sbg, Austria.
| Spatial requirements for T-cell receptor triggering probed via a DNA origami-based biointerface at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2022). A DNA origami-based biointerface for probing T-cell receptor triggering; invited talk. Gordon Research Conference on Biointerface Science, Barga-Gallicano, Italy.
| A DNA origami-based biointerface for probing T-cell receptor triggering; invited talk at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2022). A DNA origami-based biointerface for probing the spatial requirements of cell surface receptor triggering, invited talk. International Workshop “Frontiers in Physiology and Disease,” Ceske Budejovice/Czech Republic, online, Czechia.
| A DNA origami-based biointerface for probing the spatial requirements of cell surface receptor triggering, invited talk at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2022). DNA origami as a tool to study T-cell activation; invited speaker. Immuno-biophysics virtual lecture series, CNRS, Marseille, online, France.
| DNA origami as a tool to study T-cell activation; invited speaker at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2022). DNA origami as a tool to study T-cell activation; invited talk. seminar series “Selected Topics in Membrane Biophysics,” UniversitätGraz, online, Austria.
| DNA origami as a tool to study T-cell activation; invited talk at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2022). Probing the membrane environment of plasma membrane proteins; invited talk. DGfB - Membrane Biophysics Meeting, Drübeck, Germany.
| Probing the membrane environment of plasma membrane proteins; invited talk at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2022). Wie die Nanobiophysik helfen kann, unser Immunsystem und vieles mehr zu verstehen; invited speaker. “Science” forum of VHS Wien, Wien, online, Austria.
| Wie die Nanobiophysik helfen kann, unser Immunsystem und vieles mehr zu verstehen; invited speaker at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2021). A DNA origami-based biointerface for probing the spatial requirements of cell surface receptor triggering. Austrian Cluster for Tissue Regeneration Meeting, Wien, Austria.
| A DNA origami-based biointerface for probing the spatial requirements of cell surface receptor triggering at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2021). DNA origami demonstrate the unique stimulatory power of single pMHCs as T-cell antigens. Biophysical Society 65th Annual Meeting, United States of America (the).
| DNA origami demonstrate the unique stimulatory power of single pMHCs as T-cell antigens at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2021). Micro‐ and nanostructured biointerfaces for cell interaction. Habilitandenseminar der Fakultät Physik, TU-Vienna, Austria.
| Micro‐ and nanostructured biointerfaces for cell interaction at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2021). Probing the membrane environment of plasma membrane proteins; invited talk. ITN PROTON Meeting, Prague, online, Czechia.
| Probing the membrane environment of plasma membrane proteins; invited talk at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2021). Probing the membrane environment of plasma membrane proteins. 13th European Biophysics Congress (EBSA), Wien, Austria.
| Probing the membrane environment of plasma membrane proteins at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2021). Spatial requirements for T-cell receptor triggering probed via a DNA origami-based biointerface; invited talk. Purdue University, United States of America (the).
| Spatial requirements for T-cell receptor triggering probed via a DNA origami-based biointerface; invited talk at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2021). Spatial requirements for T-cell receptor triggering probed via a DNA origami-based biointerface; invited talk. seminartalk, University of Cambridge, Cambridge/UK, online, United Kingdom of Great Britain and Northern Ireland (the).
| Spatial requirements for T-cell receptor triggering probed via a DNA origami-based biointerface; invited talk at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2020). DNA origami demonstrate the unique stimulatory power of single pMHCs as T-cell antigens. Cell Bio Virtual 2020, online, United States of America (the).
| DNA origami demonstrate the unique stimulatory power of single pMHCs as T-cell antigens at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2019). DNA Origami as a nanoscale platform for T cell activation. XXIth Annual Linz Winter Workshop, Linz/ÖO, Austria.
| DNA Origami as a nanoscale platform for T cell activation at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2019). DNA origami as a nanoscale tool to study T cell activation, invited talk. SFB1032-Workshop, Benediktbeuern, Germany.
| DNA origami as a nanoscale tool to study T cell activation, invited talk at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2019). Nanoscale organization and mobility of ligands direct T cell activation. Biophysical Society 63rd Annual Meeting, Baltimore, United States of America (the).
| Nanoscale organization and mobility of ligands direct T cell activation at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2019). Nanoscale organization of ligands directs T cell activation; contributed talk. BioNanoMed 2019, Graz/Stmk, Austria.
| Nanoscale organization of ligands directs T cell activation; contributed talk at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2018). DNA Origami as a nanoscale platform for T cell activation. 8th Regional Biophysics Conference (RBC), Zrece, Slovenia.
| DNA Origami as a nanoscale platform for T cell activation at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2018). DNA origami as a nanoscale platform for T cell activation. Biophysical Society 62nd Annual Meeting, San Francisco, United States of America (the).
| DNA origami as a nanoscale platform for T cell activation at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2018). Probing lipid interactions of plasma membrane proteins: a micropatterning approach. 7th Wroclaw-Prague Seminar on Biophysics of Lipids, Wroclaw, Poland.
| Probing lipid interactions of plasma membrane proteins: a micropatterning approach at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2018). Probing lipid interactions of the T-cell receptor complex: a micropatterning approach. 20th Annual Linz Winter Workshop, Linz/OÖ, Austria.
| Probing lipid interactions of the T-cell receptor complex: a micropatterning approach at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2018). Using micro- and nanostructured biointerfaces to study plasma membrane organization and function, invited seminartalk. Invited seminar talk, DK NanoCell Colloquium, TU Wien, Austria.
| Using micro- and nanostructured biointerfaces to study plasma membrane organization and function, invited seminartalk at reposiTUm , opens an external URL in a new window
Helfert, S., Dworak, C., Sevcsik, E., Peterlik, H., Sauer, M., Ret, D., & Liska, R. (2017). Synthesis and Characterization of Polymer Linker Systems for T-cell Investigations. Workshop Additive manufacturing as a tool to create life in 3D, Brno, Czechia.
| Synthesis and Characterization of Polymer Linker Systems for T-cell Investigations at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2017). Probing the membrane environment of palmitoylated transmembrane proteins: a micropatterning approach. 9th ÖGMBT Annual Meeting 2017, Innsbruck, Austria.
| Probing the membrane environment of palmitoylated transmembrane proteins: a micropatterning approach at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2017). Probing the membrane environment of palmitoylated transmembrane proteins: a micropatterning approach. TethMem 2017, Wien, Austria.
| Probing the membrane environment of palmitoylated transmembrane proteins: a micropatterning approach at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2016). Biophysik - die Brücke zwischen Biologie und Physik; invited talk. 66th annual meeting of the Austrian Physical Society (ÖPG), Wien, Austria.
| Biophysik - die Brücke zwischen Biologie und Physik; invited talk at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2016). Combining protein micropatterning and single molecule microscopy to decipher plasma membrane organization. 8th ÖGMBT annual meeting, Graz/Stmk, Austria.
| Combining protein micropatterning and single molecule microscopy to decipher plasma membrane organization at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2016). Combining protein micropatterning and single molecule microscopy to decipher plasma membrane organization. Regional Biophysics Conference (RBC) 2016, Triest, Italy.
| Combining protein micropatterning and single molecule microscopy to decipher plasma membrane organization at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2016). GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane. Linz Winter Workshop, Linz/OÖ, Austria.
| GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane at reposiTUm , opens an external URL in a new window
Motsch, V., Hager, R., Sevcsik, E., Schäffler, F., Howorka, S., & Schütz, G. (2015). DNA origami platform for protein interaction analysis. 65th Annual Meeting of the Austrian Physical Society, Wien, Austria.
| DNA origami platform for protein interaction analysis at reposiTUm , opens an external URL in a new window
Motsch, V., Hager, R., Sevcsik, E., Schäffler, F., Howorka, S., & Schütz, G. (2015). DNA origami platform for protein interaction analysis. Biophysical Society 59th Annual Meeting, Baltimore/USA, Non-EU.
| DNA origami platform for protein interaction analysis at reposiTUm , opens an external URL in a new window
Motsch, V., Hager, R., Sevcsik, E., Schäffler, F., Howorka, S., & Schütz, G. (2015). DNA origami platform for protein interaction analysis. XVI. Annual Linz Winter Workshop 2015, Linz/OÖ, Austria.
| DNA origami platform for protein interaction analysis at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2015). Determination of the reach of a membrane proteins: is there a space for rafts?; seminartalk. Seminartalk, Universität Graz, Inst. f. Molekulare Biowissenschaften, Graz, Austria.
| Determination of the reach of a membrane proteins: is there a space for rafts?; seminartalk at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2015). GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane. 10th European Biophysics Congress, Dresden/Germany, EU.
| GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2015). GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane. 65th Annual Meeting of the Austrian Physical Society, Wien, Austria.
| GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2015). GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane. Biophysical Society 59th Annual Meeting, Baltimore/USA, Non-EU.
| GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2015). GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane. XVI. Annual Linz Winter Workshop 2015, Linz/OÖ, Austria.
| GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2015). Lipid rafts - From model membranes to live cells - Introduction to Single-molecule fluorescence microscopy techniques; invited talk. ITN SNAL Summer School on Biomaterials, Cells and Lipid Bilayers, Roccalumera/Italy, EU.
| Lipid rafts - From model membranes to live cells - Introduction to Single-molecule fluorescence microscopy techniques; invited talk at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2015). Protein micropatterning as a tool to decipher plasma membrane organization and protein interactions; invited talk. Workshop on Biomaterials and Their Interactions with Biological and Model Membranes, Salou/Spain, EU.
| Protein micropatterning as a tool to decipher plasma membrane organization and protein interactions; invited talk at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2014). Creating obstacle courses for raft proteins - How micropatterning can help decipher plasma membrane organization. Linz Winter Workshop, Linz/OÖ, Austria.
| Creating obstacle courses for raft proteins - How micropatterning can help decipher plasma membrane organization at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2014). Creating obstacle courses for raft proteins - How micropatterning can help decipher plasma membrane organization. Seminar Institut für Allgemeine Physik (IAP), TU Wien, Austria.
| Creating obstacle courses for raft proteins - How micropatterning can help decipher plasma membrane organization at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2014). Determination of the reach of membrane proteins:is there a space for rafts? 6th ÖGMBT (Österreichische Gesellschaft für Molekulare Biowissenschaften und Biotechnologie) Annual Meeting, Universitätszentrum Althanstrasse, Austria.
| Determination of the reach of membrane proteins:is there a space for rafts? at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2014). Determination of the reach of membrane proteins:is there a space for rafts? Biomembrane Days, Berlin/Germany, EU.
| Determination of the reach of membrane proteins:is there a space for rafts? at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2014). Determination of the reach of membrane proteins:is there a space for rafts? Linzer Forum Medizintechnik Medical Imaging, Linz/OÖ, Austria.
| Determination of the reach of membrane proteins:is there a space for rafts? at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2013). Protein micropatterning as a tool to decipher plasma membrane organization. Invited seminar talk, MPI für Biophysikalische Chemie, Göttingnen/D, EU.
| Protein micropatterning as a tool to decipher plasma membrane organization at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2013). Protein micropatterning in live cells: a tool for creating membrane domains with raft-like properties. Biophysical Society 57th Annual Meeting, Philadelphia, Pennsylvania/USA, Non-EU.
| Protein micropatterning in live cells: a tool for creating membrane domains with raft-like properties at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2012). Allostery in a disordered protein: Oxidative modifications to α-Synuclein act distally to regulate membrane binding. XIV Linz Winter Workshop 2012, Linz/ÖO, Austria.
| Allostery in a disordered protein: Oxidative modifications to α-Synuclein act distally to regulate membrane binding at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2012). Using protein micropatterning to probe lipid-mediated protein interactions in the plasma membrane of live cells. Arbeitsgruppentreffen der ÖGMBT Arbeitsgruppe “Single Molecule Biology,” Litschau/NÖ, Austria.
| Using protein micropatterning to probe lipid-mediated protein interactions in the plasma membrane of live cells at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2012). Using protein micropatterning to probe lipid-mediated protein interactions in the plasma membrane of live cells. Euromembrane Conference: Membrane Dynamics in Physiology and Disease, Basel/Switzerland, Non-EU.
| Using protein micropatterning to probe lipid-mediated protein interactions in the plasma membrane of live cells at reposiTUm , opens an external URL in a new window
Sevcsik, E. (2012). Using protein micropatterning to probe lipid-mediated protein interactions in the plasma membrane of live cells. LipidomicNet Workshop, TU Wien, Austria.
| Using protein micropatterning to probe lipid-mediated protein interactions in the plasma membrane of live cells at reposiTUm , opens an external URL in a new window

Articles in refereed journals

R. Platzer, J. Hellmeier, J. Göhring, I. Doel Perez, P. Schatzlmaier, C. Bodner, M. Focke-Tejkl, G.J. Schütz, E. Sevcsik, H. Stockinger, M. Brameshuber, J.B. Huppa (2023). Monomeric agonist peptide/MHCII complexes activate T-cells in an autonomous fashion. EMBO Reports e57842
J. Hellmeier, R. Platzer, J.B. Huppa, E. Sevcsik* (2023). A DNA origami-based biointerface to interrogate the spatial requirements for sensitized T-cell antigen recognition. Methods Mol. Biol. 2654, 277
I. Hartl, V. Brumovska, Y. Strieder, A. Yasari, G.J. Schütz, E. Sevcsik*, I. Tiemann-Böge* (2023) Measurement of FGFR3 signaling at the cell membrane via total internal reflection fluorescence microscopy to compare the activation of FGFR3 mutants. J. Biol. Chem. 299, 102832
J. Hellmeier, R. Platzer, V. Mühlgrabner, M.C. Schneider, E. Kurz, G.J. Schütz, J.B. Huppa, E. Sevcsik* (2021). Strategies for the site-specific decoration of DNA origami nanostructures with functionally intact proteins. ACS Nano 15, 15057
A. Schromm, L. Paulowski, Y. Kaconis, F. Kopp, M. Koistinen, A. Donoghue, S. Keese, C. Nehls, J. Wernecke, P. Garidel, E. Sevcsik, K. Lohner, S. Sanchez-Gomez, G. Martinez-de-Tejada, K. Brandenburg, M. Brameshuber, G.J. Schütz, J. Andrä, T. Gutsmann (2021). Cathelicidin and PMB neutralize endotoxins by multifactorial mechanisms including LPS interaction and targeting of host cell membranes. PNAS 118, e2101721118
J. Hellmeier, R. Platzer, A.S. Eklund, T. Schlichthärle, A. Karner, M.C. Schneider, V. Motsch, E. Kurz, V. Bamieh, M. Brameshuber, J. Preiner, R. Jungmann, H. Stockinger, G.J. Schütz, J.B. Huppa, E. Sevcsik* (2021). DNA origami demonstrate the unique stimulatory power of single pMHCs as T-cell antigens. PNAS 118, e2016857118
R. Platzer, B.K. Rossboth, M.C. Schneider, E. Sevcsik, F. Baumgart, H. Stockinger, G.J. Schütz, J.B. Huppa, M. Brameshuber (2020). Unscrambling fluorophore blinking for comprehensive cluster detection via photoactivated localization microscopy. Nature Commun. 11, 4993
A. M. Arnold, A.W.A.F. Reismann, E. Sevcsik, G.J. Schütz (2020). Monte Carlo simulations of protein micropatterning in biomembranes: effects of immobile nanofeatures with reduced diffusivity. J. Phys. D: Appl. Phys. 53, 435401
T. Váradi, M. Schneider, E. Sevcsik, D. Kiesenhofer, F. Baumgart, G. Batta, T. Kovács, R. Platzer, J.B. Huppa, J. Szöllősi, G.J. Schütz, M. Brameshuber, P. Nagy (2019). Homo- and heteroassociations drive activation of ErbB3. Biophys. J. 117, 1935
V. Motsch, M. Brameshuber, F. Baumgart, G.J. Schütz, E. Sevcsik* (2019). A micropatterning platform for quantifying interaction kinetics between the T cell receptor and an intracellular binding protein. Scientific Reports 9, 3288
M. Lindner, A. Tresztenyak, G. Fülöp, W. Jahr, A. Prinz, I. Prinz, J. Danzl, G.J. Schütz, E. Sevcsik* (2019). A fast and simple contact printing approach to generate 2D protein nanopatterns. Frontiers in Chemistry 6, 655
R. Hager, A.M. Arnold, E. Sevcsik, G.J. Schütz and S. Howorka (2018). Tunable DNA hybridization enables spatially and temporally controlled surface-anchoring of biomolecular cargo. Langmuir 34, 15021-15027
G. Fülop, M. Brameshuber, A.M. Arnold, G.J. Schütz, E. Sevcsik* (2018). Determination of the membrane environment of CD59 in living cells. Biomolecules 8, 28
M. Brameshuber, F. Kellner, B.K. Rossboth, H. Ta, K. Alge, E. Sevcsik, J. Göhring, M. Axmann, F. Baumgart, N.R.J. Gascoigne, S.J. Davis, H. Stockinger, G.J. Schütz and J.B. Huppa (2018). Monomeric TCRs drive T cell antigen recognition. Nature Immun. 19, 487-496
G.J. Schütz, J. Weghuber, P. Lanzerstorfer, E. Sevcsik* (2017). Protein Micropatterning Assay: Quantitative Analysis of Protein–Protein Interactions. Methods Mol. Biol. 1550, 261-270
A.M. Arnold, E. Sevcsik, G.J. Schütz (2016). Monte Carlo simulations of protein micropatterning in biomembranes: effects of immobile sticky obstacles. J. Phys. D: Appl. Phys. 49, 364002
E. Sevcsik* and G.J. Schütz* (2016). With or without rafts? Alternative views on cell membranes. Bioessays 38, 129-139
M. Brameshuber, E. Sevcsik, B. K. Rossboth, C. Manner, HP. Deigner, B. Peksel, M. Péter, Z. Török, A. Hermetter, G. J. Schütz (2016). Oxidized phospholipids inhibit the formation of cholesterol-dependent plasma membrane nanoplatforms. Biophys. J. 110, 205-213
E. Sevcsik*, M. Brameshuber, M. Fölser, J. Weghuber, A. Honigmann, G.J. Schütz* (2015). GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane. Nature Commun. 6, 6969
A.R. Braun, E. Sevcsik, P. Chin, E. Rhoades, S. Tristram-Nagle, J.N. Sachs (2012). α-Synuclein induces both positive mean curvature and negative Gaussian curvature in membranes. J. Am. Chem. Soc. 134, 2613
E. Sevcsik, A. Trexler, J. Dunn, E. Rhoades (2011). Evidence for allostery in a disordered protein: oxidative modifications to α-synuclein act distally to regulate membrane binding. J. Am. Chem. Soc. 133, 7152
S. Strobach, R. Kunert, J. Stadlmann, P. Messner, E. Sevcsik, G. Lhota, H. Katinger, K. Vorauer-Uhl (2009). Topological transformation of liposomes by a membrane-affecting domain of recombinant human erythropoietin, J. Liposome Res. 20, 24
E. Sevcsik*, G. Pabst, W. Richter, S. Danner, H. Amenitsch, K. Lohner (2008). Interaction of LL-37 with model membrane systems of different complexity – Influence of the lipid matrix, Biophys. J 94, 4688
E. Sevcsik, G. Pabst, A. Jilek, K. Lohner (2007). How lipids influence the mode of action of membrane-active peptides, Biochim. Biophys. Acta 1768, 2586
H. Reisinger, E. Sevcsik, K. Vorauer-Uhl, K. Lohner, H. Katinger, R. Kunert (2007). Serum-free transfection of CHO-cells with tailor-made unilamellar vesicles, Cytotechnology 54, 157
B. Pozo Navas, K. Lohner, G. Deutsch, E. Sevcsik, K.A. Riske, R. Dimova, P. Garidel, G. Pabst (2005). Composition dependence of vesicle morphology and mixing properties in a bacterial model membrane system, Biochim. Biophys. Acta 1716, 40
O. Konovalov, S.M. O’Flaherty, E. Saint-Martin, G. Deutsch, E. Sevcsik, K. Lohner (2005). The bending rigidity of phospholipid monolayers in the presence of an antimicrobial frog peptide studied by X-ray grazing incidence diffraction, Physica B 357, 185
A. Loidl, E. Sevcsik, G. Riesenhuber, H.P. Deigner, A. Hermetter (2003). Oxidized phospholipids in minimally modified low density lipoprotein induce apoptotic signaling via activation of acid sphingomyelinase in arterial smooth muscle cells, J. Biol. Chem. 278, 32921

Book contributions

K. Lohner, E. Sevcsik, G. Pabst (2007). Liposome based membrane mimetic systems: Implications for lipid-peptide interactions, in Advances in Planar Lipid Bilayers Vol. 6, (Ed. A. Leitmannova Liu), Elsevier, New York, 103

Articles in non-refereed journals

E. Sevcsik and G.J. Schütz (2017). Proteins and lipids – a complicated relationship? ASBMB Today 16, 9-10

E. Sevcsik (2021). Origami mit DNA - Wie DNA-Nanotechnologie helfen kann, unser Immunsystem besser zu verstehen.TU Wien alumni club bulletin 51, 8-9

Associate Prof. Dipl.-Ing.in Dr.in techn.Eva Sevcsik

Head of Micro- and Nanostructured Biointerfaces Group

Phone: +43 1 58801 134890 Call Eva Sevcsik

Send email to Eva Sevcsik

ORCID iD of Eva Sevcsik , opens an external URL in a new window

Research profile of Eva Sevcsik , opens an external URL in a new window

Google Scholar , opens an external URL in a new window

Associate Prof. Dipl.-Ing.in Dr.in techn.Eva Sevcsik

Head of Micro- and Nanostructured Biointerfaces Group

Phone: +43 1 58801 134890 Call Eva Sevcsik

Send email to Eva Sevcsik

ORCID iD of Eva Sevcsik , opens an external URL in a new window

Research profile of Eva Sevcsik , opens an external URL in a new window

Google Scholar , opens an external URL in a new window

Name	Purpose	Lifetime	Type	Provider
CookieConsent	Saves your settings for the use of cookies on this website.	1 year	HTML	Homepage TU Wien
SimpleSAML	This is needed to distinguish between the sessions of the logged-in users.	session	HTTP	Login TU Wien
SimpleSAMLAuthToken	This is needed to distinguish between the sessions of the logged-in users.	session	HTTP	Login TU Wien
fe_typo_user	Is needed so that in case of a Typo3 frontend login the session ID is recognized to grant access to protected areas.	session	HTTP	Homepage TU Wien
staticfilecache	Is needed to optimize the delivery time of the website.	session	HTTP	Homepage TU Wien
JESSIONSID	Is needed so that in case of a LectureTube the session ID is recognized to grant access to protected areas.	session	HTTP	LectureTube TU Wien
_shibsession_lecturetube	This is needed to distinguish between the sessions of the logged-in users.	session	HTTP	LectureTube TU Wien

Name	Purpose	Lifetime	Type	Provider
_pk_id	Used to store a few details about the user such as the unique visitor ID.	13 months	HTML	Matomo TU Wien
_pk_ref	Is used to store the information of the users home website.	6 months	HTML	Matomo TU Wien
_pk_ses	Is needed to store temporary data of the visit.	30 minutes	HTML	Matomo TU Wien
nmstat	Is used to record the behaviour on the website. It is used to collect statistics about website usage, such as when the visitor last visited the website. The cookie does not contain any personal data and is only used for website analysis.	1000 days	HTML	Siteimprove
siteimproveses	Is used to track the sequence of pages that a visitor views during his/her visit to the website. The cookie does not contain any personal data and is used solely for website analysis.	session	HTTP	Siteimprove
AWSELB	Always occurs in pairs with siteimproveses (for load balancing on the provider server)	session	HTTP	Siteimprove

Name	Purpose	Lifetime	Type	Provider
_ga	Is needed to distinguish the sessions of the users from each other.	persistent	HTTP	Google Analytics
_gali	Is needed to determine which links are clicked on a page.	expires immediately	HTTP	Google Analytics
_gat	This is a function-related cookie, whose tasks may differ.	2 years	HTTP	Google Analytics
_gid	Is needed to distinguish users and create statistics.	24 hours	HTTP	Google Analytics
_gads	Required to enable websites to display advertising from Google, including personalized advertising.	13 months	HTTP	Google Analytics
_gac_	Required by advertisers to measure user activity and the performance of their advertising campaigns.	90 days	HTTP	Google Analytics
_gcl_	Required by advertisers to determine how often users who click on their ads end up taking an action on their website.	90 days	HTTP	Google Analytics
_gcl_au	Contains a randomly generated user ID.	90 days	HTTP	Google
_gcl_aw	Is set when users click on a Google ad on the website and contains information about which ad was clicked.	90 days	HTTP	Google
__utma	Is used to record visits and visitors.	2 years	HTTP	Google Analytics
__utmb	Is used to detect new visits.	30 minutes	HTTP	Google Analytics
__utmc	Is used in connection with __utmb to determine whether it is a new (recent) visit.	session	HTTP	Google Analytics
__utmd	Is used to store and track visitor journeys through the site and classifies them into groups (marketing/tracking).	1 second	HTTP	Google Analytics
__utmt	Is needed to limit the query rate on Google Analytics.	10 minutes	HTTP	Google Analytics
__utmz	Is needed to determine from which source/campaign visitors come.	6 months	HTTP	Google Analytics
__utmvc	Is needed to collect information about user behavior on multiple websites. This information is used to optimize the relevance of advertising on the website.	24 hours	HTTP	Google AdSense
utm_source	Is needed to tag URLs with parameters to identify the campaigns that forward traffic.	expires immediately	HTTP	Google Analytics
__utm.gif	Is needed to save browser details.	session	HTTP	Google Analytics
gtag	Is needed to perform remarketing.	30 days	HTTP	Google AdSense
id	Is needed to perform remarketing.	2 years	HTTP	Google AdWords
1P_JAR	Is needed to optimize advertising, provide ads that are relevant to users, improve campaign performance reports, or prevent users from seeing the same ads more than once.	2 years	HTTP	Google
AID	Is needed to activate targeted advertising.	2 years	HTTP	Google Analytics
ANID	Is needed to display Google ads on non-Google websites.	2 years	HTTP	Google AdSense
APISID	Unknown functionality	2 years	HTTP	Google Ads Optimization
AR	Is needed to profile visitors' interests and display relevant ads on other websites. This cookie works by uniquely identifying your browser and device.	2 years	HTTP	Google AdSense
CONSENT	Is needed to store the preferences of visitors and personalize advertising.	persistent	HTTP	Google
DSID	Is needed by DoubleClick for advertising displayed in various places on the web and used to store the preferences of users.	2 years	HTTP	Doubleclick
DV	Is needed to store user preferences and other information. This includes, in particular, the preferred language, the number of search results to be displayed on the page, and the decision whether or not to activate the Google SafeSearch filter.	2 years	HTTP	Google
HSID	Contains the Google account ID and the last login time of the user.	2 years	HTTP	Google
IDE	Is needed by DoubleClick to record and report the actions of users on the website after viewing or clicking on one of the provider's ads, with the purpose of measuring the effectiveness of an advertisement and displaying targeted advertisements to users.	2 years	HTTP	Doubleclick
LOGIN_INFO	Is used to store the credentials of users of Google services.	2 years	HTTP	Google
NID	Is used to store information about user settings.	6 months	HTTP	Google
OTZ	Is needed to link activities of visitors with other devices that are previously logged in via the Google account. In this way, advertising is tailored to different devices.	1 month	HTTP	Google
RUL	Is needed by DoubleClick to determine whether advertising has been displayed correctly in order to make marketing activities more efficient.	1 year	HTTP	Doubleclick
SAPISID	Is needed by YouTube to store user settings and to calculate user bandwidth.	persistent	HTTP	Google
SEARCH_SAMESITE	Enables servers to mitigate the risk of CSRF and information leakage attacks by specifying that a particular cookie may only be sent on requests originating from the same registerable domain.	6 months	HTTP	Google
SID	Contains the Google account ID and the last login time of the user.	2 years	HTTP	Google
SIDCC	Is needed to store information about user settings and information for Google Maps.	3 months	HTTP	Google
SSID	Is needed to collect visitor information for videos hosted by YouTube on Google Maps integrated maps.	persistent	HTTP	Google
__SECURE-1PAPISID	Is needed for targeting purposes to create a profile of the interests of website visitors.	2 years	HTTP	Google
__SECURE-1PSID	Is needed for targeting purposes to create a profile of the interests of website visitors.	2 years	HTTP	Google
__SECURE-3PAPISID	Is needed for targeting purposes to create a profile of the interests of website visitors.	2 years	HTTP	Google
__SECURE-3PSID	Is needed for targeting purposes to create a profile of the interests of website visitors.	2 years	HTTP	Google
__SECURE-3PSIDCC	Is needed for targeting purposes to create a profile of the interests of website visitors.	2 years	HTTP	Google
__SECURE-APISID	Is needed to profile the interests of website visitors in order to display relevant and personalized advertising through retargeting.	8 months	HTTP	Google
__SECURE-HSID	Is needed to secure digitally signed and encrypted data from the unique Google ID and to store the last login time that Google uses to identify visitors, prevent fraudulent use of login data, and protect visitor data from unauthorized parties. This may also be used for targeting purposes to display relevant and personalized advertising content.	8 months	HTTP	Google
__SECURE-SSID	Is needed to store information about how visitors use the site and about the ads they may have seen before visiting the site. Also used to customize ads on Google domains.	8 months	HTTP	Google
test_cookie	Is set as a test to check whether the browser allows cookies to be set. Does not contain any identification features.	15 minutes	HTTP	Google
VISITOR_INFO1_LIVE	Is needed by YouTube to store user settings and to calculate user bandwidth.	6 months	HTTP	Youtube
facebook	Is used to Enable ad delivery or retargeting	90 days	HTTP	Meta (Facebook)
__fb_chat_plugin	Is needed to store and track interactions (marketing/tracking).	persistent	HTTP	Meta (Facebook)
_js_datr	Is needed to save user settings.	2 years	HTTP	Meta (Facebook)
_fbc	Is needed to save the last visit (marketing/tracking).	2 years	HTTP	Meta (Facebook)
fbm	Is needed to store account data (marketing/tracking).	1 year	HTTP	Meta (Facebook)
xs	Is needed to store a unique session ID (marketing/tracking).	1 year	HTTP	Meta (Facebook)
wd	Is needed to log the screen resolution.	1 week	HTTP	Meta (Facebook)
fr	Is needed to serve ads and measure and improve their relevance.	3 months	HTTP	Meta (Facebook)
act	Is needed to store logged in users (marketing/tracking).	90 days	HTTP	Meta (Facebook)
_fbp	Is needed to store and track visits to various websites (marketing/tracking).	3 months	HTTP	Meta (Facebook)
datr	Is needed to identify the browser for security and website integrity purposes, including account recovery and identification of potentially compromised accounts.	2 years	HTTP	Meta (Facebook)
dpr	Is used for analysis purposes. Technical parameters are logged (e.g. aspect ratio and dimensions of the screen) so that Facebook apps can be displayed correctly.	1 week	HTTP	Meta (Facebook)
sb	Is needed to store browser details and security information of the Facebook account.	2 years	HTTP	Meta (Facebook)
dbln	Is needed to store browser details and security information of the Facebook account.	2 years	HTTP	Meta (Facebook)
spin	Is needed for promotional purposes and social campaign reporting.	session	HTTP	Meta (Facebook)
presence	Contains the "chat" status of logged in users.	1 month	HTTP	Meta (Facebook)
cppo	Is needed for statistical purposes.	90 days	HTTP	Meta (Facebook)
locale	Is needed to save the language settings.	session	HTTP	Meta (Facebook)
pl	Required for Facebook Pixel.	2 years	HTTP	Meta (Facebook)
lu	Required for Facebook Pixel.	2 years	HTTP	Meta (Facebook)
c_user	Required for Facebook Pixel.	3 months	HTTP	Meta (Facebook)
bcookie	Is needed to store browser data (marketing/tracking).	2 years	HTTP	LinkedIn
li_oatml	Is needed to identify LinkedIn members outside of LinkedIn for advertising and analytics purposes.	1 month	HTTP	LinkedIn
BizographicsOptOut	Is needed to save privacy settings.	10 years	HTTP	LinkedIn
li_sugr	Is needed to store browser data (marketing/tracking).	3 months	HTTP	LinkedIn
UserMatchHistory	Is needed to provide advertising or retargeting (marketing/tracking).	30 days	HTTP	LinkedIn
linkedin_oauth_	Is needed to provide cross-page functionality.	session	HTTP	LinkedIn
lidc	Is needed to store performed actions on the website (marketing/tracking).	1 day	HTTP	LinkedIn
bscookie	Is needed to store performed actions on the website (marketing/tracking).	2 years	HTTP	LinkedIn
X-LI-IDC	Is needed to provide cross-page functionality (marketing/tracking).	session	HTTP	LinkedIn
AnalyticsSyncHistory	Stores the time when the user was synchronized with the "lms_analytics" cookie.	30 days	HTTP	LinkedIn
lms_ads	Is needed to identify LinkedIn members outside of LinkedIn.	30 days	HTTP	LinkedIn
lms_analytics	Is needed to identify LinkedIn members for analytics purposes.	30 days	HTTP	LinkedIn
li_fat_id	Required for indirect member identification used for conversion tracking, retargeting and analytics.	30 days	HTTP	LinkedIn
U	Is needed to identify the browser.	3 months	HTTP	LinkedIn
_guid	Is needed to identify a LinkedIn member for advertising via Google Ads.	90 days	HTTP	LinkedIn

Publications, Articles & Talks

Publications

Articles

Books & Book Contributions

Inproceedings

Preprints

Talks

Articles in refereed journals

Book contributions

Articles in non-refereed journals

Associate Prof. Dipl.-Ing.in Dr.in techn.Eva Sevcsik

Associate Prof. Dipl.-Ing.in Dr.in techn.Eva Sevcsik