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DTSTART;TZID=Europe/Paris:20241115T110000
DTEND;TZID=Europe/Paris:20241115T110000
DTSTAMP:20260503T154646
CREATED:20240527T054803Z
LAST-MODIFIED:20241111T185156Z
UID:13478-1731668400-1731668400@ibv.unice.fr
SUMMARY:Johannes BROICHHAGEN
DESCRIPTION:From: FMP\, Berlin \n  \nWill give a seminar entitled: \n  \nChemical Biology Approaches to interrogate G Protein-Coupled Receptors \n  \nLabelling\, visualization\, and functional manipulation of biomolecules is at the forefront of chemical biology.[1\,2] However\, selective and quantitative interrogation and analysis of biomolecules remains a challenge in the field. To tackle these issues\, we employ approaches from photopharmacology\, molecular biology and fluorophore design to enable biomolecule labelling and control in specific sites while elevating dye properties to the next level. To allow outstanding image quality\, we designed and synthesized custom-tailored fluorophore substrates to advance photophysical and chemical properties to discern protein pools\, such as the plasma membrane-bound and intracellular populations.[3] In a similar vein\, we pursue unconventional strategies to design and synthesize fluorophores for super-resolution imaging in live cells. In one of our latest study\, we installed carbon-deuterium bonds in fluorophores.[4] This simple modification yields dyes with increased fluorescent lifetimes\, higher photostability\, and enhanced brightness\, improving nanoscopy and single molecule tracking. With this in hand\, we focus on cell surface proteins\, such as beta-secretase (BACE1) and the glucagon-like peptide 1 receptor (GLP1R). While the former is an important protease involved in the progression of Alzheimer’s disease\, the latter is a class B GPCR that is involved in glucose homeostasis and satiety and a blockbuster target to treat patients suffering from type 2 diabetes. As such\, it becomes incredibly important to unravel their fine interplay with custom-designed chemical biology probes. We highlight GLP1R in its endogenous context with fluorescently labelled antagonist – the LUXendins – that target the orthosteric site\, allowing super resolution imaging\, 2-photon imaging\, single particle tracking and intravital microscopy in vivo.[5] With an expanded color palette\, we enabled the use of NIR light for imaging.[6] We next genetically engineered an enzyme self-label onto GLP1R to interrogate its localization and behavior in its native context on the endogenous level.[7] This allows the tracking of GLP1R in the complex tissue setting versus different type of drugs. Taken together\, we aim to use chemistry as a flashlight to shine a spotlight on the invisible in biological systems. \n  \nReferences\n[1]        L. Xue\, I. A. Karpenko\, J. Hiblot\, K. Johnsson\, Nat. Chem. Biol. 2015\, 11\, 917–23.\n[2]        S. J. Sahl\, S. W. Hell\, S. Jakobs\, Nat. Rev. Mol. Cell Biol. 2017\, 18\, 685–701.\n[3]        R. Birke\, J. Ast\, D. A. Roosen\, J. Lee\, K. Roßmann\, C. Huhn\, B. Mathes\, M. Lisurek\, D. Bushiri\, H. Sun\, B. Jones\, M. Lehmann\, J. Levitz\, V. Haucke\, D. J. Hodson\, J. Broichhagen\, Org Biomol Chem 2022\, 20\, 5967–5980.\n[4]        K. Roßmann\, K. C. Akkaya\, P. Poc\, C. Charbonnier\, J. Eichhorst\, H. Gonschior\, A. Valavalkar\, N. Wendler\, T. Cordes\, B. Dietzek-Ivanšić\, B. Jones\, M. Lehmann\, J. Broichhagen\, Chem Sci 2022\, 13\, 8605–8617.\n[5]        J. Ast\, A. Arvaniti\, N. H. F. Fine\, D. Nasteska\, F. B. Ashford\, Z. Stamataki\, Z. Koszegi\, A. Bacon\, B. J. Jones\, M. A. Lucey\, S. Sasaki\, D. I. Brierley\, B. Hastoy\, A. Tomas\, G. D’Agostino\, F. Reimann\, F. C. Lynn\, C. A. Reissaus\, A. K. Linnemann\, E. D’Este\, D. Calebiro\, S. Trapp\, K. Johnsson\, T. Podewin\, J. Broichhagen\, D. J. Hodson\, Nat Commun 2020\, 11\, 467.\n[6]        J. Ast\, A. N. Novak\, T. Podewin\, N. H. F. Fine\, B. Jones\, A. Tomas\, R. Birke\, K. Roßmann\, B. Mathes\, J. Eichhorst\, M. Lehmann\, A. K. Linnemann\, D. J. Hodson\, J. Broichhagen\, JACS Au 2022\, 2\, 1007–1017.\n[7]        J. Ast\, D. Nasteska\, N. H. F. Fine\, D. J. Nieves\, Z. Koszegi\, Y. Lanoiselée\, F. Cuozzo\, K. Viloria\, A. Bacon\, N. T. Luu\, P. N. Newsome\, D. Calebiro\, D. M. Owen\, J. Broichhagen\, D. J. Hodson\, Nat Commun 2023\, 14\, 301. \n  \nSpeaker website
URL:http://ibv.unice.fr/event/johannes-broichhagen-2/
LOCATION:Salle de Conférences\, Centre de Biochimie\, 28 avenue Valrose\, Faculté des Sciences\, Parc Valrose\, Nice\, 06100\, France
CATEGORIES:Seminar Series
ORGANIZER;CN="Guillaume%20SANDOZ":MAILTO:sandoz@unice.fr
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