EXC 115: Dynamik Makromolekularer Komplexe
Zusammenfassung der Projektergebnisse
Der Exzellenzcluster Frankfurt „Macromolecular Complexes" (CEF) wurde 2006 von der Goethe-Universität gemeinsam mit den Max-Planck-Instituten für Biophysik und Hirnforschung gegründet. CEF holte weitere exzellente Wissenschaftlerinnen und Wissenschaftler nach Frankfurt und gründete das Buchmann Institut für Molekulare Lebenswissenschaften (BMLS) nach einem erfolgreichen Forschungsgebäudeantrag beim Wissenschaftsrat. Das BMLS ist eine hochmoderne Forschungseinrichtung, die Forschungsgruppen aus vier Fakultäten der Universität beherbergt. CEF hat die technologische Infrastruktur in Frankfurt durch den Kauf neuer Geräte verbessert. Das Frankfurt Center for Advanced Light Microscopy und das Frankfurt Center for Electron Microscopy befinden sich im BMLS und wurden von Wissenschaftlern gegründet, die durch CEF eingestellt wurden. CEF förderte den wissenschaftlichen Austausch durch eine Reihe von Programmen sowie durch Workshops, internationale Konferenzen, öffentliche Vortragsreihen und Faculty Dinners. Mitglieder des CEF veröffentlichten während der Laufzeit des Clusters mehr als 2600 Original-Forschungspublikationen (darunter 479 Veröffentlichungen mit einem Impact Faktor von ≥10). Die Struktur und Funktion wichtiger makromolekularer Komplexe wurden von CEF auf atomarer Auflösung bestimmt, so z.B. von Komplex I und der ATP-Synthase der mitochondrialen Atmungskette sowie des eukaryotischen Antigenpeptid-Transporter TAP. Die Erforschung der Struktur und Funktion von RNA führte zur Definition von regulatorischen Prinzipien von Riboswitches, der Struktur-Funktionsbeziehung der RNA-Polymerase I, der Funktionen von microRNAs, sowie der Mechanismen der rRNA-Reifung und der nachgelagerten Prozesse während der Biogenese und des Recyclings von Ribosomen. CEF-Mitglieder identifizierten die Rezeptoren für Ubiquitinketten auf dem Proteasom, entschlüsselten die Rolle linearer Ubiquitinketten und beschrieben Makromoleküle, die Mitophagie, Xenophagie und ER-phagie regulieren. Sie beschrieben die Rolle der SUMOylierung bei der Qualitätskontrolle von Ribosomen und charakterisierten den Prozess der genetischen Qualitätskontrolle bei Eizellen. Die Forschung in diesen drei Forschungsbereichen wurde durch Arbeiten zum Design oder zur Neuprogrammierung makromolekularer Komplexe und durch die Entwicklung neuer Methoden begleitet. Mitglieder des CEF haben die Prinzipien der Optogenetik sowie biochemische Methoden zur Lichtregulierung etabliert und weiterentwickelt. Sie entwickelten zudem weitere biophysikalische Methoden zur strukturellen und funktionellen Charakterisierung von Makromolekülen, z.B. für Anwendungen in der Zelle geeignete lichtschaltbare Moleküle sowie zeitaufgelöste Methoden zur Untersuchung der RNA-Faltung. Die Lichtscheibenmikroskopie zur Beobachtung von Entwicklungvorgängen und die LILBID-Massenspektrometrie zur Analyse von Membrankomplexen wurden weiterentwickelt. PELDOR-EPR wurde zu einer Auflösung entwickelt, die sogar Messungen in der Zelle ermöglicht.
Link zum Abschlussbericht
https://dx.doi.org/10.2314/GBV:1696608775
Projektbezogene Publikationen (Auswahl)
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(2007) Native protein nanolithography that can write, read and erase. Nat Nanotechnol 2: 220-225
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(2008) 4-Chloro-α-cyanocinnamic acid is an advanced, rationally designed MALDI matrix. P Natl Acad Sci USA 105: 12200-12205
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(2008) Optogenetic analysis of synaptic function. Nat Methods 5: 895 - 902
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(2008) Proteasome subunit Rpn13 is a novel ubiquitin receptor. Nature 453: 481-488
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(2008) Serine phosphorylation of ephrinB2 regulates trafficking of synaptic AMPA receptors. Nat Neurosci 11: 1035-1043
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(2008) Structural basis for the selectivity of the external thioesterase of the surfactin synthetase. Nature 454: 907-911
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(2008) The oxazolidinone antibiotics perturb the ribosomal peptidyl-transferase center and effect tRNA positioning. P Natl Acad Sci USA 105: 13339-13344
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(2008) The structure of the neuropeptide bradykinin bound to the human G-protein coupled receptor bradykinin B2 as determined by solid-state NMR spectroscopy. Angew Chem Int Edit 47: 1668-1671
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(2011) Realtime multimodal optical control of neurons and muscles in freely behaving Caenorhabditis elegans. Nat Methods 8: 153-U78
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(2011) SHARPIN forms a linear ubiquitin ligase complex regulating NF-kappa B activity and apoptosis. Nature 471: 637-641
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(2011) Solution NMR structure of proteorhodopsin. Angew Chem Int Edit 50: 11942-11946
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(2011) Structural basis for tail-anchored membrane protein biogenesis by the Get3-receptor complex. Science 333: 758-762
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(2011) The threedimensional molecular structure of the desmosomal plaque. P Natl Acad Sci USA 108: 6480-6485
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(2011) Ultra light-sensitive and fast neuronal activation with the Ca(2+)-permeable channelrhodopsin CatCh. Nat Neurosci 14: 513-518
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(2012) Complexome profiling identifies TMEM126B as a component of the mitochondrial complex I assembly complex. Cell Metab 16: 538-549
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(2012) Fluorescence-based sensors to monitor localization and functions of linear and K63-linked ubiquitin chains in cells. Mol Cell 47: 797-809
van Wijk SJL, Fiskin E, Putyrski M, Pampaloni F, Hou J, Wild P, Kensche T, Grecco HE, Bastiaens P, Dikic I
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(2012) Ultrafast dynamics of a spiropyran in water. J Am Chem Soc 134: 14070-14077
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2012) Transport of drugs by the multidrug transporter AcrB involves an access and a deep binding pocket that are separated by a switch-loop. P Natl Acad Sci USA 109: 5687-5692
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(2013) MicroRNA-34a regulates cardiac ageing and function. Nature 495: 107-110
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(2013) Three-state mechanism couples ligand and temperature sensing in riboswitches. Nature 499: 355-U135
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(2015) Design of photocaged puromycin for nascent polypeptide release and spatiotemporal monitoring of translation. Angew Chem Int Edit 54: 3717-3721
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(2015) Direct visualization of newly synthesized target proteins in situ. Nat Methods 12: 411-114
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(2015) Enlightening the photoactive site of channelrhodopsin-2 by DNP-enhanced solid-state NMR spectroscopy. P Natl Acad Sci USA 112: 9896-9901
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(2015) Horizontal membraneintrinsic alpha-helices in the stator a-subunit of an F-type ATP synthase. Nature 521: 237-240
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(2015) Identification and characterization of hypoxia-regulated endothelial circular RNA. Circ Res 117: 884-890
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(2015) Influence of arrestin on the photodecay of bovine rhodopsin. Angew Chem Int Edit 54: 13555-13560
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(2015) Involvement of long-lived intermediate states in the complex folding pathway of the human telomeric G-quadruplex. Angew Chem Int Edit 54: 8444-8448
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(2015) Live imaging of Tribolium castaneum embryonic development using light-sheet-based fluorescence microscopy. Nat Protoc 10: 1486-1507
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(2015) Mechanistic insight from the crystal structure of mitochondrial complex I. Science 347: 44-49
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(2015) Optogenetic manipulation of cGMP in cells and animals by the tightly light-regulated guanylyl-cyclase opsin CyclOp. Nat Commun 6: article 8046
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(2016) Structure of a bd oxidase indicates similar mechanisms for membraneintegrated oxygen reductases. Science 352: 583-586
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(2017) Activity-dependent spatially localized miRNA maturation in neuronal dendrites. Science 355: 634-637
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(2017) Cryo-EM structure of the TOM core complex from Neurospora crassa. Cell 170: 693-700.e7
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(2017) Crystal structure and mechanistic basis of a functional homolog of the antigen transporter TAP. P Natl Acad Sci USA 114: E438–E447
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(2017) Structure of the 40S-ABCE1 post-splitting complex in ribosome recycling and translation initiation. Nat Struct Mol Biol 24: 453–460
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(2017) Structure of the human MHC-I peptide-loading complex. Nature 551: 525–528
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(2018) Chemo-enzymatic synthesis of position-specifically modified RNA for biophysical studies including light control and NMR spectroscopy. Angew Chem Int Ed 57: 12017-12021
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(2018) Endothelial Dab1 signalling orchestrates neuro-glia-vessel communication in the central nervous system. Science 361: eaao2861
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(2018) Food sensation modulates locomotion by dopamine and neuropeptide signalling in a distributed neuronal network. Neuron 100: 1414-1428.e10
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(2018) Insights into catalysis and function of phosphoribosyl-linked serine ubiquitination. Nature 557: 734-738
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(2018) Locking loop movement in the ubiquinone pocket of complex I disengages the proton pumps. Nat Commun 9: 4500
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(2018) Plant-specific ribosome biogenesis factors in Arabidopsis thaliana with essential function in rRNA processing. Nucleic Acids Res 47: 1880–1895
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