| Literature DB >> 30799880 |
Toshio Ando1, Satya Prathyusha Bhamidimarri2, Niklas Brending3, H Colin-York4, Lucy Collinson5, Niels De Jonge6,7, P J de Pablo8,9, Elke Debroye10, Christian Eggeling4,11,12,13, Christian Franck14, Marco Fritzsche4,15, Hans Gerritsen16, Ben N G Giepmans17, Kay Grunewald18,19,20, Johan Hofkens10, Jacob P Hoogenboom21,22, Kris P F Janssen10, Rainer Kaufman18,19,23, Judith Klumpermann24, Nyoman Kurniawan25, Jana Kusch26, Nalan Liv24, Viha Parekh25, Diana B Peckys27, Florian Rehfeldt28, David C Reutens25, Maarten B J Roeffaers29, Tim Salditt30, Iwan A T Schaap31,32, Ulrich S Schwarz33, Paul Verkade34, Michael W Vogel25, Richard Wagner2, Mathias Winterhalter2, Haifeng Yuan10, Giovanni Zifarelli35.
Abstract
Developments in microscopy have been instrumental to progress in the life sciences, and many new techniques have been introduced and led to new discoveries throughout the last century. A wide and diverse range of methodologies is now available, including electron microscopy, atomic force microscopy, magnetic resonance imaging, small-angle x-ray scattering and multiple super-resolution fluorescence techniques, and each of these methods provides valuable read-outs to meet the demands set by the samples under study. Yet, the investigation of cell development requires a multi-parametric approach to address both the structure and spatio-temporal organization of organelles, and also the transduction of chemical signals and forces involved in cell-cell interactions. Although the microscopy technologies for observing each of these characteristics are well developed, none of them can offer read-out of all characteristics simultaneously, which limits the information content of a measurement. For example, while electron microscopy is able to disclose the structural layout of cells and the macromolecular arrangement of proteins, it cannot directly follow dynamics in living cells. The latter can be achieved with fluorescence microscopy which, however, requires labelling and lacks spatial resolution. A remedy is to combine and correlate different readouts from the same specimen, which opens new avenues to understand structure-function relations in biomedical research. At the same time, such correlative approaches pose new challenges concerning sample preparation, instrument stability, region of interest retrieval, and data analysis. Because the field of correlative microscopy is relatively young, the capabilities of the various approaches have yet to be fully explored, and uncertainties remain when considering the best choice of strategy and workflow for the correlative experiment. With this in mind, the Journal of Physics D: Applied Physics presents a special roadmap on the correlative microscopy techniques, giving a comprehensive overview from various leading scientists in this field, via a collection of multiple short viewpoints.Entities:
Keywords: atomic force microscopy; correlative microscopy; electron microscopy; fluorescence microscopy; magnetic resonance imaging; super-resolution microscopy; x-ray microscopy
Year: 2018 PMID: 30799880 PMCID: PMC6372154 DOI: 10.1088/1361-6463/aad055
Source DB: PubMed Journal: J Phys D Appl Phys ISSN: 0022-3727 Impact factor: 3.207