Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Ulrike, Zabel"'
Autor:
Irene Fasciani, Francesco Petragnano, Ziming Wang, Ruairidh Edwards, Narasimha Telugu, Ilaria Pietrantoni, Ulrike Zabel, Henrik Zauber, Marlies Grieben, Maria E Terzenidou, Jacopo Di Gregorio, Cristina Pellegrini, Silvano Santini, Anna R Taddei, Bärbel Pohl, Stefano Aringhieri, Marco Carli, Gabriella Aloisi, Francesco Marampon, Eve Charlesworth, Alexandra Roman, Sebastian Diecke, Vincenzo Flati, Franco Giorgi, Fernanda Amicarelli, Andrew B Tobin, Marco Scarselli, Kostas Tokatlidis, Mario Rossi, Martin J Lohse, Paolo Annibale, Roberto Maggio
Publikováno v:
PLoS Biology, Vol 22, Iss 4, p e3002582 (2024)
Muscarinic acetylcholine receptors are prototypical G protein-coupled receptors (GPCRs), members of a large family of 7 transmembrane receptors mediating a wide variety of extracellular signals. We show here, in cultured cells and in a murine model,
Externí odkaz:
https://doaj.org/article/55337ca4f8c84555b649a08804c2bd5c
Autor:
Raphael S. Haider, Edda S. F. Matthees, Julia Drube, Mona Reichel, Ulrike Zabel, Asuka Inoue, Andy Chevigné, Cornelius Krasel, Xavier Deupi, Carsten Hoffmann
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-17 (2022)
Here the authors present improved intramolecular sensors for β-arrestin2 and 1, which enable assessment of conformational changes of both isoforms in living cells. These reveal that the same GPCR induces differential conformational rearrangements th
Externí odkaz:
https://doaj.org/article/c788b6ac74db47fe8176035c251fe6d0
Autor:
Katarina Nemec, Hannes Schihada, Gunnar Kleinau, Ulrike Zabel, Eugene O. Grushevskyi, Patrick Scheerer, Martin J. Lohse, Isabella Maiellaro
Publikováno v:
PNAS
Receptor-activity-modifying proteins (RAMPs) are ubiquitously expressed membrane proteins that associate with different G protein–coupled receptors (GPCRs), including the parathyroid hormone 1 receptor (PTH1R), a class B GPCR and an important modul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97453c7e0840f3ac28d8ba9214ce4728
http://edoc.mdc-berlin.de/21973/1/21973oa.pdf
http://edoc.mdc-berlin.de/21973/1/21973oa.pdf
Autor:
Henry F. Vischer, Steffen Pockes, Martin J. Lohse, Gunnar Schulte, Hannes Schihada, Ulrike Zabel, Rob Leurs, Xiaoyuan Ma
Publikováno v:
ACS Sensors
ACS Sensors, 5(6), 1734-1742. American Chemical Society
Schihada, H, Ma, X, Zabel, U, Vischer, H F, Schulte, G, Leurs, R, Pockes, S & Lohse, M J 2020, ' Development of a Conformational Histamine H 3 Receptor Biosensor for the Synchronous Screening of Agonists and Inverse Agonists ', ACS Sensors, vol. 5, no. 6, pp. 1734-1742 . https://doi.org/10.1021/acssensors.0c00397
ACS Sensors, 5(6), 1734-1742. American Chemical Society
Schihada, H, Ma, X, Zabel, U, Vischer, H F, Schulte, G, Leurs, R, Pockes, S & Lohse, M J 2020, ' Development of a Conformational Histamine H 3 Receptor Biosensor for the Synchronous Screening of Agonists and Inverse Agonists ', ACS Sensors, vol. 5, no. 6, pp. 1734-1742 . https://doi.org/10.1021/acssensors.0c00397
The histamine H(3) receptor (H(3)R) represents a highly attractive drug target for the treatment of various central nervous system disorders, but the discovery of novel H(3)R targeting compounds relies on the assessment of highly amplified intracellu
Autor:
Katarina Nemec, Hannes Schihada, Gunnar Kleinau, Ulrike Zabel, Eugene O. Grushevskyi, Patrick Scheerer, Martin J. Lohse, Isabella Maiellaro
Receptor-activity-modifying proteins (RAMPs) are ubiquitously expressed membrane proteins that associate with different G protein-coupled receptors (GPCRs) including the parathyroid hormone 1 receptor (PTH1R), a class B GPCR and an important modulato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b1b7dabd434e2aa882b569a809a94e6
https://doi.org/10.1101/2021.12.08.471790
https://doi.org/10.1101/2021.12.08.471790
Autor:
Ralf Schmauder, Martin J. Lohse, Tina Schwabe, Ulrike Zabel, Eugene O. Grushevskyi, Klaus Benndorf, Taulant Kukaj, Andreas Bock
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Significance G protein-coupled receptors (GPCRs) form a family of signaling molecules in the membrane of cells that plays a key role in transduction of cellular responses. Little is known about how rapidly GPCRs can be activated. While the “light r
Autor:
Santini S, Andrew B. Tobin, Pöhl B, Cristina Pellegrini, Irene Fasciani, Francesco Petragnano, Jacopo Di Gregorio, Ulrike Zabel, Amicarelli F, Henrik Zauber, Giorgi F, Ilaria Pietrantoni, Martin J. Lohse, Sebastian Diecke, Wang Z, Francesco Marampon, Konstantinos Tokatlidis, Stefano Aringhieri, Telegu N, A. R. Taddei, Gabriella Aloisi, Roman A, Terzenidou Me, Grieben M, Roberto Maggio, Paolo Annibale, Marco Scarselli, Mario Rossi, Flati, Robert Edwards
Muscarinic acetylcholine receptors are prototypical G protein-coupled receptors (GPCRs), members of a large family of seven transmembrane receptors that mediates a wide variety of extracellular signals. We show here, for the first time in a GPCR, tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e7b08ccaed2acc7a9bbb11aafcd0876
https://doi.org/10.1101/2021.04.13.438299
https://doi.org/10.1101/2021.04.13.438299
Autor:
Romy Thomas, Ulrike Zabel, Jan Möller, Irene Coin, Paolo Annibale, Marco Scarselli, Annette G. Beck-Sickinger, Chiara De Faveri, Ali Işbilir, Martin J. Lohse, Andreas Bock, Robert Serfling
Publikováno v:
Nature protocols. 16(3)
Oligomerization of membrane proteins has received intense research interest because of their importance in cellular signaling and the large pharmacological and clinical potential this offers. Fluorescence imaging methods are emerging as a valid tool
Autor:
Ulrike Zabel, Carsten Hoffmann, Jessika Klöckner, Susanne Nuber, Michael Kauk, Regina Messerer, Maria Consuelo Alonso Canizal, Daniela Volpato, Ulrike Holzgrabe
Publikováno v:
ACS Chemical Biology. 12:833-843
Aiming to design partial agonists as well as allosteric modulators for the M1 muscarinic acetylcholine (M1AChR) receptor, two different series of bipharmacophoric ligands and their structural analogues were designed and synthesized. The hybrids were
Autor:
Charlotte Konrad, Paolo Annibale, Andreas Bock, Ulrike Zabel, Martin J. Lohse, Isabella Maiellaro, Martin Falcke, Sivaraj Sivaramakrishnan, Annette Hannawacker, Selma E. Anton
Publikováno v:
Cell
Cells relay a plethora of extracellular signals to specific cellular responses using only a few second messengers, such as cAMP. To explain signaling specificity, cAMP-degrading phosphodiesterases (PDEs) have been suggested to confine cAMP to distinc