Research Topics
| Markus HussSummaryCountry: Germany Publications
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Detail Information
Publications
Concanamycin A, the specific inhibitor of V-ATPases, binds to the V(o) subunit cMarkus Huss
, Fachbereich Biologie/Chemie, Abteilung Tierphysiologie, , Germany
J Biol Chem 277:40544-8. 2002..Binding was also prevented by the plecomacrolides bafilomycin A(1) and B(1), respectively, but not by the benzolactone enamide salicylihalamide, a member of a novel class of V-ATPase inhibitors...
Archazolid A binds to the equatorial region of the c-ring of the vacuolar H+-ATPaseSvenja Bockelmann
Universitat Osnabruck, Fachbereich Biologie chemie, Abteilung Tierphysiologie, Barbarastrasse 11, 49069 Osnabruck, Germany
J Biol Chem 285:38304-14. 2010..This hypothesis was supported by an additional subset of mutations within helix 4 that revealed that leucine 144 plays a role in archazolid binding...
Vacuolar H(+)-ATPases: intra- and intermolecular interactionsMarkus Huss
University of Osnabruck, Faculty of Biology and Chemistry, Department of Animal Physiology, Barbarastrasse 11, 49076 Osnabruck, Germany
Eur J Cell Biol 90:688-95. 2011..Both features require distinct intramolecular as well as intermolecular interactions. Here we will summarize our own results together with newer developments in both of these research areas...
Archazolid and apicularen: novel specific V-ATPase inhibitorsMarkus Huss
Universitat Osnabruck, Fachbereich Biologie chemie, Abteilung Tierphysiologie, 49069 Osnabruck, Germany
BMC Biochem 6:13. 2005..Since their malfunction is correlated with various diseases in humans, the elucidation of the properties of this enzyme for the development of selective inhibitors and drugs is one of the challenges in V-ATPase research...
Inhibitors of V-ATPases: old and new playersMarkus Huss
Department of Biology Chemistry, University of Osnabruck, 49069 Osnabruck, Germany
J Exp Biol 212:341-6. 2009....
Influence of ATP and ADP on dissociation of the V-ATPase into its V(1) and V(O) complexesMarkus Huss
Fachbereich Biologie chemie, Abteilung Tierphysiologie, Universitat Osnabruck, 49069, Osnabruck, Germany
FEBS Lett 581:5566-72. 2007..Incubation of the V(1)V(O) holoenzyme with various adenine nucleotides revealed that ATP hydrolysis, leading to a state containing tightly bound ADP is necessary for its dissociation...
The binding site of the V-ATPase inhibitor apicularen is in the vicinity of those for bafilomycin and archazolidChristin Osteresch
Fachbereich Biologie chemie, Abteilung Tierphysiologie, Universitat Osnabruck, Barbarastrasse 11, 49069 Osnabruck, German
J Biol Chem 287:31866-76. 2012..Therefore, the binding site of benzolactone enamides cannot be formed exclusively by subunit c. Apparently, subunit a substantially contributes to the binding of the benzolactone enamides...
Vacuolar-type proton pumps in insect epitheliaHelmut Wieczorek
Department of Biology Chemistry, University of Osnabruck, 49069 Osnabruck, Germany
J Exp Biol 212:1611-9. 2009..Finally we review an integrated physiological approach in Malpighian tubules of the yellow fever mosquito Aedes aegypti which shows that the V-ATPase delivers the energy for both transcellular and paracellular ion transport...
The insect plasma membrane H+ V-ATPase: intra-, inter-, and supramolecular aspectsHelmut Wieczorek
Department of Biology Chemistry, University of Osnabruck, 49069 Osnabruck, Germany
J Bioenerg Biomembr 35:359-66. 2003....
Cruentaren A, a highly cytotoxic benzolactone from Myxobacteria is a novel selective inhibitor of mitochondrial F1-ATPasesBrigitte Kunze
Arbeitsgruppe Mikrobielle Kommunikation, Helmholtz Zentrum für Infektionsforschung, 38124 Braunschweig, Germany
FEBS Lett 581:3523-7. 2007..Since mitochondrial ATPases play a crucial role in the pathophysiology of several human disorders including cancer, cruentaren or synthetic derivatives thereof could form the basis of future therapeutic strategies...
The first hydroxylated archazolid from the myxobacterium Cystobacter violaceus: isolation, structural elucidation and V-ATPase inhibitionDirk Menche
Helmholtz Zentrum für Infektionsforschung GmbH, Medicinal Chemistry and Chemical Biology, Braunschweig, Germany
J Antibiot (Tokyo) 60:328-31. 2007..This novel metabolite was evaluated for growth inhibition of murine connective tissue cells and V-ATPase inhibition in comparison to other known archazolids...
Design, synthesis, and biological evaluation of novel analogues of archazolid: a highly potent simplified V-ATPase inhibitorDirk Menche
Helmholtz Zentrum für Infektionsforschung GmbH, Medizinische Chemie, Inhoffenstrasse 7, 38124 Braunschweig, Germany
Bioorg Med Chem Lett 17:1732-5. 2007....
Cruentaren, a new antifungal salicylate-type macrolide from Byssovorax cruenta (myxobacteria) with inhibitory effect on mitochondrial ATPase activity. Fermentation and biological propertiesBrigitte Kunze
Helmholtz Centre for Infection Research, Inhoffenstrasse 7, D 38124 Braunschweig, Germany
J Antibiot (Tokyo) 59:664-8. 2006..Cruentaren A inhibited F0F1 mitochondrial ATP-hydrolysis in submitochondrial particles of yeasts and beef heart...
The V-type H(+)-ATPase in Malpighian tubules of Aedes aegypti: localization and activityXing-He Weng
Department of Biomedical Sciences, Cornell University, Ithaca, NY 14853, USA
J Exp Biol 206:2211-9. 2003..Measures of transepithelial Na(+) and K(+) secretion and estimates of the H(+) flux mediated by the V-type H(+)-ATPase suggest a 1:1 stoichiometry for Na(+)/H(+) and K(+)/H(+) exchange transport across the apical membrane...
