Advances in molecular probe-based labeling tools and their application to multiscale multimodal correlated microscopies
The need to determine the precise subcellular distribution of specific proteins and macromolecular complexes in cells and tissues has been the major driving force behind the development of new molecular-genetic and chemical-labeling approaches applicable to high-resolution, correlated, multidimensio...
| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
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Springer Berlin Heidelberg
2016
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| Online Access: | http://hdl.handle.net/1721.1/105352 https://orcid.org/0000-0002-8277-5226 |
| _version_ | 1826216546343583744 |
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| author | Phan, S. Boassa, D. Ellisman, M. H. Deerinck, T. J. Kim, K. Y. Bushong, E. A. Ting, Alice Y |
| author2 | Massachusetts Institute of Technology. Department of Chemistry |
| author_facet | Massachusetts Institute of Technology. Department of Chemistry Phan, S. Boassa, D. Ellisman, M. H. Deerinck, T. J. Kim, K. Y. Bushong, E. A. Ting, Alice Y |
| author_sort | Phan, S. |
| collection | MIT |
| description | The need to determine the precise subcellular distribution of specific proteins and macromolecular complexes in cells and tissues has been the major driving force behind the development of new molecular-genetic and chemical-labeling approaches applicable to high-resolution, correlated, multidimensional microscopy. This short review is intended to provide an overview of recently developed and widely used electron microscopy (EM)-compatible probes, including tetracysteine tags, mini singlet oxygen generator (MiniSOG), time-specific tag for the age measurement of proteins (TimeSTAMP) with MiniSOG, and enhanced ascorbate peroxidase (APEX). We describe how these highly specific and genetically introduced EM probes are now used, in conjunction with lower resolution light microscopic methods, to obtain wide field or dynamic records of live preparation or of large maps in 3D using recently developed laboratory-scale X-ray microscopes. The article is intended to enable researchers through a high-level view of the toolbox of labels available today for studies aiming to analyze dynamic subcellular and molecular processes in cell culture systems as well as in animal tissues—and ultimately allow investigators to determine the precise location of macromolecular complexes by EM. |
| first_indexed | 2024-09-23T16:49:21Z |
| format | Article |
| id | mit-1721.1/105352 |
| institution | Massachusetts Institute of Technology |
| language | English |
| last_indexed | 2024-09-23T16:49:21Z |
| publishDate | 2016 |
| publisher | Springer Berlin Heidelberg |
| record_format | dspace |
| spelling | mit-1721.1/1053522022-09-29T21:45:25Z Advances in molecular probe-based labeling tools and their application to multiscale multimodal correlated microscopies Phan, S. Boassa, D. Ellisman, M. H. Deerinck, T. J. Kim, K. Y. Bushong, E. A. Ting, Alice Y Massachusetts Institute of Technology. Department of Chemistry Ting, Alice Y The need to determine the precise subcellular distribution of specific proteins and macromolecular complexes in cells and tissues has been the major driving force behind the development of new molecular-genetic and chemical-labeling approaches applicable to high-resolution, correlated, multidimensional microscopy. This short review is intended to provide an overview of recently developed and widely used electron microscopy (EM)-compatible probes, including tetracysteine tags, mini singlet oxygen generator (MiniSOG), time-specific tag for the age measurement of proteins (TimeSTAMP) with MiniSOG, and enhanced ascorbate peroxidase (APEX). We describe how these highly specific and genetically introduced EM probes are now used, in conjunction with lower resolution light microscopic methods, to obtain wide field or dynamic records of live preparation or of large maps in 3D using recently developed laboratory-scale X-ray microscopes. The article is intended to enable researchers through a high-level view of the toolbox of labels available today for studies aiming to analyze dynamic subcellular and molecular processes in cell culture systems as well as in animal tissues—and ultimately allow investigators to determine the precise location of macromolecular complexes by EM. 2016-11-17T23:18:22Z 2016-11-17T23:18:22Z 2015-05 2015-02 2016-08-18T15:37:02Z Article http://purl.org/eprint/type/JournalArticle 1864-6158 1864-6166 http://hdl.handle.net/1721.1/105352 Ellisman, M. H. et al. “Advances in Molecular Probe-Based Labeling Tools and Their Application to Multiscale Multimodal Correlated Microscopies.” Journal of Chemical Biology 8.4 (2015): 143–151. https://orcid.org/0000-0002-8277-5226 en http://dx.doi.org/10.1007/s12154-015-0132-6 Journal of Chemical Biology Creative Commons Attribution-Noncommercial-Share Alike http://creativecommons.org/licenses/by-nc-sa/4.0/ Springer-Verlag Berlin Heidelberg application/pdf Springer Berlin Heidelberg Springer Berlin Heidelberg |
| spellingShingle | Phan, S. Boassa, D. Ellisman, M. H. Deerinck, T. J. Kim, K. Y. Bushong, E. A. Ting, Alice Y Advances in molecular probe-based labeling tools and their application to multiscale multimodal correlated microscopies |
| title | Advances in molecular probe-based labeling tools and their application to multiscale multimodal correlated microscopies |
| title_full | Advances in molecular probe-based labeling tools and their application to multiscale multimodal correlated microscopies |
| title_fullStr | Advances in molecular probe-based labeling tools and their application to multiscale multimodal correlated microscopies |
| title_full_unstemmed | Advances in molecular probe-based labeling tools and their application to multiscale multimodal correlated microscopies |
| title_short | Advances in molecular probe-based labeling tools and their application to multiscale multimodal correlated microscopies |
| title_sort | advances in molecular probe based labeling tools and their application to multiscale multimodal correlated microscopies |
| url | http://hdl.handle.net/1721.1/105352 https://orcid.org/0000-0002-8277-5226 |
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