Emmanuel G. Reynaud
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Emmanuel G. Reynaud has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
- Miguel A. Andrade-Navarro
Johannes Gutenberg University of Mainz
2 shared publications Christiane Jost
Cell Biology and Cell Biophysics Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany
1 shared publication- Claudia Chica
Institut Pasteur Université Paris Cité Paris France
1 shared publication - Ernst Hans Karl Stelzer
Buchmann Institute for Molecular Life Sciences (BMLS), Goethe Universität Frankfurt am Main
1 shared publication - Fabien Bonneau
Department of Structural Cell Biology, Max Planck Institute of Biochemistry
1 shared publication - Gareth A. Palidwor
Ottawa Hospital Research Institute, Ottawa, ON K1R 6M1, Canada
1 shared publication
Latest Publications
- 1 October 2008
- Published by Taylor & Francis in HFSP Journal
- Vol. 2 (5) , 266-275
Light sheet‐based fluorescence microscopy: More dimensions, more photons, and less photodamage
Light‐sheet‐based fluorescence microscopy (LSFM) is a fluorescence technique that combines optical sectioning, the key capability of confocal and two‐photon fluorescence microscopes with multiple‐view imaging, which is used in optical tomography. In contrast to conventional wide‐field and confocal fluorescence microscopes, a light sheet illuminates only the focal plane of the detection objective lens from the side. Excitation is, thus, restricted to the fluorophores in the volume near the focal plane. This provides optical sectioning and allows the use of regular cameras in the detection process. Compared to confocal fluorescence microscopy, LSFM reduces photo bleaching and photo toxicity by up to three orders of magnitude. In LSFM, the specimen is embedded in a transparent block of hydrogel and positioned relative to the stationary light sheet using precise motorized translation and rotation stages. This feature is used to image any plane in a specimen. Additionally, multiple views obtained along differe...
- 1 October 2008
- Published by Taylor & Francis in HFSP Journal
- Vol. 2 (5) , 266-275
Light sheet‐based fluorescence microscopy: More dimensions, more photons, and less photodamage
Light‐sheet‐based fluorescence microscopy (LSFM) is a fluorescence technique that combines optical sectioning, the key capability of confocal and two‐photon fluorescence microscopes with multiple‐view imaging, which is used in optical tomography. In contrast to conventional wide‐field and confocal fluorescence microscopes, a light sheet illuminates only the focal plane of the detection objective lens from the side. Excitation is, thus, restricted to the fluorophores in the volume near the focal plane. This provides optical sectioning and allows the use of regular cameras in the detection process. Compared to confocal fluorescence microscopy, LSFM reduces photo bleaching and photo toxicity by up to three orders of magnitude. In LSFM, the specimen is embedded in a transparent block of hydrogel and positioned relative to the stationary light sheet using precise motorized translation and rotation stages. This feature is used to image any plane in a specimen. Additionally, multiple views obtained along differe...
- 11 December 2006
- Published by Wiley in Biotechnology Journal
- Vol. 1 (12) , 1347-1350
Adéquation Germany, meeting the needs of scientists in the developing world
- 11 December 2006
- Published by Wiley in Biotechnology Journal
- Vol. 1 (12) , 1347-1350
Adéquation Germany, meeting the needs of scientists in the developing world
- Open Access
- 17 February 2006
- Published by Springer Nature in BMC Bioinformatics
- Vol. 7 (1) , 79
Taxonomic colouring of phylogenetic trees of protein sequences
Background Phylogenetic analyses of protein families are used to define the evolutionary relationships between homologous proteins. The interpretation of protein-sequence phylogenetic trees requires the examination of the taxonomic properties of the species associated to those sequences. However, there is no online tool to facilitate this interpretation, for example, by automatically attaching taxonomic information to the nodes of a tree, or by interactively colouring the branches of a tree according to any combination of taxonomic divisions. This is especially problematic if the tree contains on the order of hundreds of sequences, which, given the accelerated increase in the size of the protein sequence databases, is a situation that is becoming common. Results We have developed PhyloView, a web based tool for colouring phylogenetic trees upon arbitrary taxonomic properties of the species represented in a protein sequence phylogenetic tree. Provided that the tree contains SwissProt, SpTrembl, or GenBank protein identifiers, the tool retrieves the taxonomic information from the corresponding database. A colour picker displays a summary of the findings and allows the user to associate colours to the leaves of the tree according to any number of taxonomic partitions. Then, the colours are propagated to the branches of the tree. Conclusion PhyloView can be used at http://www.ogic.ca/projects/phyloview/. A tutorial, the software with documentation, and GPL licensed source code, can be accessed at the same web address.
- 17 February 2006
- Published by Springer Nature in BMC Bioinformatics
- Vol. 7 (1) , 79
Open AccessTaxonomic colouring of phylogenetic trees of protein sequences
Background Phylogenetic analyses of protein families are used to define the evolutionary relationships between homologous proteins. The interpretation of protein-sequence phylogenetic trees requires the examination of the taxonomic properties of the species associated to those sequences. However, there is no online tool to facilitate this interpretation, for example, by automatically attaching taxonomic information to the nodes of a tree, or by interactively colouring the branches of a tree according to any combination of taxonomic divisions. This is especially problematic if the tree contains on the order of hundreds of sequences, which, given the accelerated increase in the size of the protein sequence databases, is a situation that is becoming common. Results We have developed PhyloView, a web based tool for colouring phylogenetic trees upon arbitrary taxonomic properties of the species represented in a protein sequence phylogenetic tree. Provided that the tree contains SwissProt, SpTrembl, or GenBank protein identifiers, the tool retrieves the taxonomic information from the corresponding database. A colour picker displays a summary of the findings and allows the user to associate colours to the leaves of the tree according to any number of taxonomic partitions. Then, the colours are propagated to the branches of the tree. Conclusion PhyloView can be used at http://www.ogic.ca/projects/phyloview/. A tutorial, the software with documentation, and GPL licensed source code, can be accessed at the same web address.
- Open Access
- 7 October 2005
- Published by Springer Nature in BMC Biology
- Vol. 3 (1) , 21
Human Lsg1 defines a family of essential GTPases that correlates with the evolution of compartmentalization
Background Compartmentalization is a key feature of eukaryotic cells, but its evolution remains poorly understood. GTPases are the oldest enzymes that use nucleotides as substrates and they participate in a wide range of cellular processes. Therefore, they are ideal tools for comparative genomic studies aimed at understanding how aspects of biological complexity such as cellular compartmentalization evolved. Results We describe the identification and characterization of a unique family of circularly permuted GTPases represented by the human orthologue of yeast Lsg1p. We placed the members of this family in the phylogenetic context of the YlqF Related GTPase (YRG) family, which are present in Eukarya, Bacteria and Archea and include the stem cell regulator Nucleostemin. To extend the computational analysis, we showed that hLsg1 is an essential GTPase predominantly located in the endoplasmic reticulum and, in some cells, in Cajal bodies in the nucleus. Comparison of localization and siRNA datasets suggests that all members of the family are essential GTPases that have increased in number as the compartmentalization of the eukaryotic cell and the ribosome biogenesis pathway have evolved. Conclusion We propose a scenario, consistent with our data, for the evolution of this family: cytoplasmic components were first acquired, followed by nuclear components, and finally the mitochondrial and chloroplast elements were derived from different bacterial species, in parallel with the formation of the nucleolus and the specialization of nuclear components.
- 7 October 2005
- Published by Springer Nature in BMC Biology
- Vol. 3 (1) , 21
Open AccessHuman Lsg1 defines a family of essential GTPases that correlates with the evolution of compartmentalization
Background Compartmentalization is a key feature of eukaryotic cells, but its evolution remains poorly understood. GTPases are the oldest enzymes that use nucleotides as substrates and they participate in a wide range of cellular processes. Therefore, they are ideal tools for comparative genomic studies aimed at understanding how aspects of biological complexity such as cellular compartmentalization evolved. Results We describe the identification and characterization of a unique family of circularly permuted GTPases represented by the human orthologue of yeast Lsg1p. We placed the members of this family in the phylogenetic context of the YlqF Related GTPase (YRG) family, which are present in Eukarya, Bacteria and Archea and include the stem cell regulator Nucleostemin. To extend the computational analysis, we showed that hLsg1 is an essential GTPase predominantly located in the endoplasmic reticulum and, in some cells, in Cajal bodies in the nucleus. Comparison of localization and siRNA datasets suggests that all members of the family are essential GTPases that have increased in number as the compartmentalization of the eukaryotic cell and the ribosome biogenesis pathway have evolved. Conclusion We propose a scenario, consistent with our data, for the evolution of this family: cytoplasmic components were first acquired, followed by nuclear components, and finally the mitochondrial and chloroplast elements were derived from different bacterial species, in parallel with the formation of the nucleolus and the specialization of nuclear components.