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Natalia H. Revelo
Researcher at Radboud University Nijmegen
Publications - 20
Citations - 903
Natalia H. Revelo is an academic researcher from Radboud University Nijmegen. The author has contributed to research in topics: Endosome & Golgi apparatus. The author has an hindex of 12, co-authored 19 publications receiving 678 citations. Previous affiliations of Natalia H. Revelo include University of Göttingen.
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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.
Journal ArticleDOI
A new probe for super-resolution imaging of membranes elucidates trafficking pathways
Natalia H. Revelo,Dirk Kamin,Sven Truckenbrodt,Aaron B. Wong,Kirsten Reuter-Jessen,Ellen Reisinger,Tobias Moser,Silvio O. Rizzoli +7 more
TL;DR: mCLING is a novel membrane probe for the study of membrane trafficking with demonstrated value in both live and fixed cells across a wide range of biological systems.
Journal ArticleDOI
Lipid peroxidation causes endosomal antigen release for cross-presentation.
Ilse Dingjan,Daniëlle R J Verboogen,Laurent M. Paardekooper,Natalia H. Revelo,Simone P. Sittig,Linda J. Visser,Gabriele Fischer von Mollard,Stefanie S. V. Henriet,Carl G. Figdor,Martin ter Beest,Geert van den Bogaart +10 more
TL;DR: It is shown that reactive oxygen species (ROS) produced by the NADPH-oxidase complex NOX2 cause lipid peroxidation, a membrane disrupting chain-reaction, which in turn results in antigen leakage from endosomes, a new cellular function for ROS in regulating immune responses against pathogens and cancer.
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Disruption of adaptor protein 2μ (AP-2μ) in cochlear hair cells impairs vesicle reloading of synaptic release sites and hearing.
SangYong Jung,SangYong Jung,Tanja Maritzen,Tanja Maritzen,Carolin Wichmann,Zhizi Jing,Andreas Neef,Natalia H. Revelo,Hanan Al-Moyed,Sandra Meese,Sonja M. Wojcik,Iliana Panou,Haydar Bulut,Peter Schu,Ralf Ficner,Ellen Reisinger,Silvio O. Rizzoli,Jakob Neef,Jakob Neef,Nicola Strenzke,Volker Haucke,Volker Haucke,Tobias Moser +22 more
TL;DR: It is reported that the endocytic adaptor protein 2μ (AP‐2μ) is required for release site replenishment and hearing, and proposed that binding of AP‐2 to otoferlin facilitates replenishment of release sites, for example, via speeding AZ clearance of exocytosed material.
Journal ArticleDOI
Endosomal and Phagosomal SNAREs
Ilse Dingjan,Peter T. A. Linders,Daniëlle R J Verboogen,Natalia H. Revelo,Martin ter Beest,Geert van den Bogaart +5 more
TL;DR: An overview of the SNAREs involved in endosomal and phagosomal trafficking is provided to provide an overview of how these proteins are targeted by viruses and intracellular pathogens.