List of Publications Prof. Dr. Thomas Brüser


Showing entries 21 - 30 out of 51
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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.

doi.org/10.1002/cbic.201300778

Taubert, J., & Brüser, T. (2014). Twin-arginine translocation-arresting protein regions contact TatA and TatB. Biological Chemistry, 395(7-8), 827-836.

doi.org/10.1515/hsz-2014-0170


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.

doi.org/10.1021/la204473t

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.

doi.org/10.1074/jbc.M112.374983


2011


Hou, B., & Brüser, T. (2011). The Tat-dependent protein translocation pathway. Biomolecular Concepts, 2(6), 507-523.

doi.org/10.1515/BMC.2011.040


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.

doi.org/10.1016/j.febslet.2010.07.039


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.

doi.org/10.1111/j.1574-6968.2009.01600.x

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.

doi.org/10.1016/j.jmb.2009.01.034


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.

doi.org/10.1074/jbc.M707757200


Showing entries 21 - 30 out of 51
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