List of Publications Prof. Dr. Thomas Brüser
2014
Niggemann, J., Bozko, P., Bruns, N., Wodtke, A., Gieseler, M. T., Thomas, K., Jahns, C., Nimtz, M., Reupke, I., Brüser, T., Auling, G., Malek, N., & Kalesse, M. (2014). Baceridin, a cyclic hexapeptide from an epiphytic bacillus strain, inhibits the proteasome. CHEMBIOCHEM, 15(7), 1021-1029.
Taubert, J., & Brüser, T. (2014). Twin-arginine translocation-arresting protein regions contact TatA and TatB. Biological Chemistry, 395(7-8), 827-836.
2012
Brehmer, T., Kerth, A., Graubner, W., Malesevic, M., Hou, B., Brüser, T., & Blume, A. (2012). Negatively charged phospholipids trigger the interaction of a bacterial tat substrate precursor protein with lipid monolayers. LANGMUIR, 28(7), 3534-3541.
Mehner, D., Osadnik, H., Lünsdorf, H., & Brüser, T. (2012). The Tat system for membrane translocation of folded proteins recruits the membrane-stabilizing Psp machinery in Escherichia coli. Journal of Biological Chemistry, 287(33), 27834-27842.
2011
Hou, B., & Brüser, T. (2011). The Tat-dependent protein translocation pathway. Biomolecular Concepts, 2(6), 507-523.
2010
Lindenstrauß, U., Matos, C. F. R. O., Graubner, W., Robinson, C., & Brüser, T. (2010). Malfolded recombinant Tat substrates are Tat-independently degraded in Escherichia coli. FEBS letters, 584(16), 3644-3648.
2009
Brüser, T. (2009). Künstliche Substrate zur Charakterisierung des Tat-Transports. BioSpektrum, 2009(11), 768-769.
Lindenstrauß, U., & Brüser, T. (2009). Tat transport of linker-containing proteins in Escherichia coli. FEMS Microbiology Letters, 295(1), 135-140.
Weininger, U., Haupt, C., Schweimer, K., Graubner, W., Kovermann, M., Brüser, T., Scholz, C., Schaarschmidt, P., Zoldak, G., Schmid, F. X., & Balbach, J. (2009). NMR solution structure of SlyD from Escherichia coli: Spatial Separation of Prolyl Isomerase and Chaperone Function. Journal of Molecular Biology, 387(2), 295-305.
2008
Berthelmann, F., Mehner, D., Richter, S., Lindenstrauss, U., Lünsdorf, H., Hause, G., & Brüser, T. (2008). Recombinant expression of tatABC and tatAC results in the formation of interacting cytoplasmic TatA tubes in Escherichia coli. Journal of Biological Chemistry, 283(37), 25281-25289.