M
Marcel A. Lauterbach
Researcher at Max Planck Society
Publications - 32
Citations - 3220
Marcel A. Lauterbach is an academic researcher from Max Planck Society. The author has contributed to research in topics: STED microscopy & Microscopy. The author has an hindex of 18, co-authored 30 publications receiving 2802 citations. Previous affiliations of Marcel A. Lauterbach include Paris Descartes University & French Institute of Health and Medical Research.
Papers
More filters
Journal ArticleDOI
Video-Rate Far-Field Optical Nanoscopy Dissects Synaptic Vesicle Movement
Volker Westphal,Silvio O. Rizzoli,Marcel A. Lauterbach,Dirk Kamin,Reinhard Jahn,Stefan W. Hell +5 more
TL;DR: This study demonstrates the emerging ability of optical microscopy to investigate intracellular physiological processes on the nanoscale in real time and map and describe the vesicle mobility within the highly confined space of synaptic boutons.
Journal ArticleDOI
Regulation of exosome secretion by Rab35 and its GTPase-activating proteins TBC1D10A–C
Chieh Hsu,Yuichi Morohashi,Shin-ichiro Yoshimura,Natalia Manrique-Hoyos,SangYong Jung,Marcel A. Lauterbach,Mostafa Bakhti,Mads Grønborg,Wiebke Möbius,Jeong-Seop Rhee,Francis A. Barr,Mikael Simons +11 more
TL;DR: A screen in oligodendrocytes establishes a Rab family member and its GAPs as regulators of exosome secretion by controlling endocytic vesicle docking with the plasma membrane.
Proceedings ArticleDOI
Far-Field Optical Nanoscopy
TL;DR: The first technique developed is STED, which recently has progressed to video-rate imaging of living cells as mentioned in this paper, which is one of the emerging fields in microscopy, and fluorophore switching is key.
Journal ArticleDOI
Spatially Stable Mitochondrial Compartments Fuel Local Translation during Plasticity.
TL;DR: It is found that local translation in neurons is powered by mitochondria and not by glycolysis, and results indicate that cytoskeletally tethered local energy compartments exist in dendrites to fuel local translation during synaptic plasticity.
Journal ArticleDOI
Glyoxal as an alternative fixative to formaldehyde in immunostaining and super-resolution microscopy.
Katharina N. Richter,Natalia H. Revelo,Katharina J. Seitz,Martin S. Helm,Deblina Sarkar,Rebecca Sonia Saleeb,Elisa D’Este,Jessica Eberle,Eva Wagner,Christian Vogl,Christian Vogl,Diana F. Lázaro,Diana F. Lázaro,Frank Richter,Javier Coy-Vergara,Giovanna Coceano,Edward S. Boyden,Rory R. Duncan,Stefan W. Hell,Marcel A. Lauterbach,Stephan E. Lehnart,Tobias Moser,Tobias Moser,Tiago F. Outeiro,Tiago F. Outeiro,Peter Rehling,Peter Rehling,Blanche Schwappach,Ilaria Testa,Bolek Zapiec,Silvio O. Rizzoli +30 more
TL;DR: Glyoxal acted faster than PFA, cross‐linked proteins more effectively, and improved the preservation of cellular morphology, suggesting that glyoxal can be a valuable alternative to PFA for immunostaining.