My Research Interest in RESIST |
Our aim in the context of RESIST is the development of new antiviral, antimicrobial and immunomodulatory agents that target the innate immune sensors cyclic GMP-AMP synthase (cGAS) and 2′-5′-oligoadenylate synthase (OAS). OAS and cGAS belong to the large and diverse superfamily of nucleotide triphosphate transferases. Both enzymes play key roles in the activation of interferon- driven antiviral responses upon recognition of pathogen-associated molecular patterns (PAMPs). In addition, these sensors constitute a continuous surveillance system for the presence of microorganisms in tissues.
We use a structure-based approach for the identification and optimization of highly specific small-molecule allosteric effectors of cGAS and OAS. This work is based on our comprehensive structural and mechanistic description of the complete enzymatic cycle of human cGAS and OAS. Validation of the compounds is performed in collaboration with RESIST scientists Thomas Pietschmann and Ulrich Kalinke.
Prof. Manstein about his scientific work
Prof. Dr. Dietmar Manstein – Curriculum Vitae
Current Position
Undergraduate and Postgraduate Training
Academic and Research Posts
Other Scientific Roles
Awards and Prizes
Granted Patents

10 Selected Publications (of > 118 original publications)
Bratanov, D., Kovalev, K., Machtens, J.P., Astashkin, R., Chizhov, I., Soloviov, D., Volkov, D., Polovinkin, V., Zabelskii, D., Mager, T., Gushchin, I., Rokitskaya, T., Antonenko, Y., Alekseev, A., Shevchenko, V., Yutin, N., Rosselli, R., Baeken, C., Borshchevskiy, V., Bourenkov, G., Popov, A., Balandin, T., Buldt, G., Manstein, D.J., Rodriguez-Valera, F., Fahlke, C., Bamberg, E., Koonin, E. and Gordeliy, V. Unique structure and function of viral rhodopsins. Nat Commun 2019; 10: 4939. Doi: 10.1038/s41467-019-12718-0
Latham, S.L., Ehmke, N., Reinke, P.Y.A., Taft, M.H., Eicke, D., Reindl, T., Stenzel, W., Lyons, M.J., Friez, M.J., Lee, J.A., Hecker, R., Fruhwald, M.C., Becker, K., Neuhann, T.M., Horn, D., Schrock, E., Niehaus, I., Sarnow, K., Grutzmann, K., Gawehn, L., Klink, B., Rump, A., Chaponnier, C., Figueiredo, C., Knofler, R., Manstein, D.J.*, Di Donato, N.* Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia. Nat Commun 2018; 9: 4250. Doi: 10.1038/s41467-018-06713-0 *joint senior author
Chinthalapudi K, Heissler SM, Preller M, Sellers JR, Manstein DJ. Mechanistic Insights into the Active Site and Allosteric Communication Pathways in Human Nonmuscle Myosin-2C. Elife 2017; 6. Doi: 10.7554/eLife.32742.
von der Ecken, J., Heissler, S.M., Pathan-Chhatbar, S., Manstein, D.J., Raunser, S. Cryo-EM structure of a human cytoplasmic actomyosin complex at near-atomic resolution. Nature 2016; 534: 724-728. Doi: 10.1038/nature18295
Hundt, N., Steffen, W., Pathan-Chhatbar, S., Taft, M.H., Manstein, D.J. Load-dependent modulation of non- muscle myosin-2A function by tropomyosin 4.2. Sci Rep 2016; 6: 20554. Doi: 10.1038/srep20554
Lohöfener, J., Steinke, N., Kay-Fedorov, P., Baruch, P., Nikulin, A., Tishchenko, S., Manstein, D.J., and Fedorov, R. The Activation Mechanism of 2′-5′-Oligoadenylate Synthetase Gives New Insights Into OAS/cGAS Triggers of Innate Immunity. Structure 2015; 23(5): 851-62. Doi: 10.1016/j.str.2015.03.012
Radke, M.B., Taft, M.H., Stapel, B., Hilfiker-Kleiner, D., Preller, M., Manstein, D.J. Small molecule-mediated refolding and activation of myosin motor function. Elife 2014; 3. Doi: 10.7554/eLife.01603
Behrmann, E., Müller, M., Penczek, P.A., Mannherz, H.G., Manstein, D.J.*, Raunser, S.* Structure of the rigor actin-tropomyosin-myosin complex. Cell 2012; 150: 327-338. Doi: 10.1016/j.bpj.2011.11.3105 *joint senior author
Fedorov, R., Böhl, M., Tsiavaliaris, G., Hartmann, F.K., Taft, M.H., Baruch, P., Brenner, B., Martin, R., Knölker, H.-J., Gutzeit, H.O., Manstein, D.J. The mechanism of pentabromopseudilin inhibition of myosin motor activity. Nat Struct Mol Biol 2009; 16: 80-88. Doi: 10.1038/nsmb.1542
Tsiavaliaris, G., Fujita-Becker, S., Manstein, D.J. Molecular engineering of a backwards-moving myosin motor. Nature 2004; 427: 558-561. Doi: 10.1038/nature02303
