Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Lioudmila, Zoubak"'
Autor:
Johanna Becker-Baldus, Alexei Yeliseev, Thomas T. Joseph, Snorri Th. Sigurdsson, Lioudmila Zoubak, Kirk Hines, Malliga R. Iyer, Arjen van den Berg, Sam Stepnowski, Jon Zmuda, Klaus Gawrisch, Clemens Glaubitz
Publikováno v:
ACS Omega, Vol 8, Iss 36, Pp 32963-32976 (2023)
Externí odkaz:
https://doaj.org/article/543ddeac6e3345cbaafa6a8240ec5d13
Autor:
Alexei Yeliseev, Malliga R. Iyer, Thomas T. Joseph, Nathan J. Coffey, Resat Cinar, Lioudmila Zoubak, George Kunos, Klaus Gawrisch
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-18 (2021)
Abstract Signaling through integral membrane G protein-coupled receptors (GPCRs) is influenced by lipid composition of cell membranes. By using novel high affinity ligands of human cannabinoid receptor CB2, we demonstrate that cholesterol increases b
Externí odkaz:
https://doaj.org/article/f7405dfa40aa4301afa918bbd3f3c38d
Autor:
Lioudmila Zoubak, Roderic G. Eckenhoff, Weiming Bu, Grace Brannigan, Alexei Yeliseev, Thomas T. Joseph, Renyu Liu, Wenzhen Lin
Publikováno v:
ACS Chemical Neuroscience
Ketamine is an anesthetic, analgesic, and antidepressant whose secondary metabolite (2R,6R)-hydroxynorketamine (HNK) has N-methyl-d-aspartate-receptor-independent antidepressant activity in a rodent model. In humans, naltrexone attenuates its antidep
Publikováno v:
Journal of Biological Chemistry. 295:181-190
G protein–coupled receptors (GPCRs) comprise a large class of integral membrane proteins involved in the regulation of a broad spectrum of physiological processes and are a major target for pharmaceutical drug development. Structural studies can he
Autor:
George Kunos, Thomas T. Joseph, Resat Cinar, Klaus Gawrisch, Nathan J. Coffey, Lioudmila Zoubak, Alexei Yeliseev, Malliga R. Iyer
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-18 (2021)
Scientific Reports
Scientific Reports
Signaling through integral membrane G protein-coupled receptors (GPCRs) is influenced by lipid composition of cell membranes. By using novel high affinity ligands of human cannabinoid receptor CB2, we demonstrate that cholesterol increases basal acti
Site-selective labeling and electron paramagnetic resonance studies of human cannabinoid receptor CB
Autor:
Alexei A, Yeliseev, Kaeli, Zoretich, Levi, Hooper, Walter, Teague, Lioudmila, Zoubak, Kirk G, Hines, Klaus, Gawrisch
Publikováno v:
Biochim Biophys Acta Biomembr
Integral membrane G protein-coupled receptors (GPCR) regulate multiple physiological processes by transmitting signals from extracellular milieu to intracellular proteins and are major targets of pharmaceutical drug development. Since GPCR are inhere
Autor:
Kyle Williston, Alexei Yeliseev, Arjen van den Berg, Lioudmila Zoubak, Wanhua Yan, Sam Stepnowski, Jonathan Zmuda, Kirk G. Hines, Klaus Gawrisch
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-15 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-15 (2020)
Rational design of pharmaceutical drugs targeting integral membrane G protein-coupled receptors (GPCR) requires thorough understanding of ligand binding and mechanism of activation through high resolution structural studies of purified proteins. Due
Autor:
Alexei Yeliseev, Kaeli Zoretich, Levi Hooper, Walter E. Teague, Lioudmila Zoubak, Kirk G. Hines, Klaus Gawrisch
Publikováno v:
Biophysical Journal. 121:85a
Autor:
Sara Linse, Lioudmila Zoubak, Niamh Ní Mhurchú, David J. O'Connell, Alexei Yeliseev, Gavin McGauran
Publikováno v:
Biochemistry. 57:4383-4390
The process of isolating recombinant G protein-coupled receptors from membrane preparations is challenging because the process requires solubilization in detergent micelles and multistep affinity chromatography protocols. Solubilization buffers conta
Autor:
Kirk G. Hines, Alexei Yeliseev, Klaus Gawrisch, Walter E. Teague, Levi Hooper, Lioudmila Zoubak, Kaeli Zoretich
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Biomembranes. 1863:183621
Integral membrane G protein-coupled receptors (GPCR) regulate multiple physiological processes by transmitting signals from extracellular milieu to intracellular proteins and are major targets of pharmaceutical drug development. Since GPCR are inhere