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MIiSR: Molecular Interactions in Super-Resolution Imaging Enables the Analysis of Protein Interactions, Dynamics and Formation of Multi-protein Structures

Our current understanding of the molecular mechanisms which regulate cellular processes such as vesicular trafficking has been enabled by conventional biochemical and microscopy techniques. However, these methods often obscure the heterogeneity of the cellular environment, thus precluding a quantita...

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Autores principales: Caetano, Fabiana A., Dirk, Brennan S., Tam, Joshua H. K., Cavanagh, P. Craig, Goiko, Maria, Ferguson, Stephen S. G., Pasternak, Stephen H., Dikeakos, Jimmy D., de Bruyn, John R., Heit, Bryan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676698/
https://www.ncbi.nlm.nih.gov/pubmed/26657340
http://dx.doi.org/10.1371/journal.pcbi.1004634
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author Caetano, Fabiana A.
Dirk, Brennan S.
Tam, Joshua H. K.
Cavanagh, P. Craig
Goiko, Maria
Ferguson, Stephen S. G.
Pasternak, Stephen H.
Dikeakos, Jimmy D.
de Bruyn, John R.
Heit, Bryan
author_facet Caetano, Fabiana A.
Dirk, Brennan S.
Tam, Joshua H. K.
Cavanagh, P. Craig
Goiko, Maria
Ferguson, Stephen S. G.
Pasternak, Stephen H.
Dikeakos, Jimmy D.
de Bruyn, John R.
Heit, Bryan
author_sort Caetano, Fabiana A.
collection PubMed
description Our current understanding of the molecular mechanisms which regulate cellular processes such as vesicular trafficking has been enabled by conventional biochemical and microscopy techniques. However, these methods often obscure the heterogeneity of the cellular environment, thus precluding a quantitative assessment of the molecular interactions regulating these processes. Herein, we present Molecular Interactions in Super Resolution (MIiSR) software which provides quantitative analysis tools for use with super-resolution images. MIiSR combines multiple tools for analyzing intermolecular interactions, molecular clustering and image segmentation. These tools enable quantification, in the native environment of the cell, of molecular interactions and the formation of higher-order molecular complexes. The capabilities and limitations of these analytical tools are demonstrated using both modeled data and examples derived from the vesicular trafficking system, thereby providing an established and validated experimental workflow capable of quantitatively assessing molecular interactions and molecular complex formation within the heterogeneous environment of the cell.
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spelling pubmed-46766982015-12-31 MIiSR: Molecular Interactions in Super-Resolution Imaging Enables the Analysis of Protein Interactions, Dynamics and Formation of Multi-protein Structures Caetano, Fabiana A. Dirk, Brennan S. Tam, Joshua H. K. Cavanagh, P. Craig Goiko, Maria Ferguson, Stephen S. G. Pasternak, Stephen H. Dikeakos, Jimmy D. de Bruyn, John R. Heit, Bryan PLoS Comput Biol Research Article Our current understanding of the molecular mechanisms which regulate cellular processes such as vesicular trafficking has been enabled by conventional biochemical and microscopy techniques. However, these methods often obscure the heterogeneity of the cellular environment, thus precluding a quantitative assessment of the molecular interactions regulating these processes. Herein, we present Molecular Interactions in Super Resolution (MIiSR) software which provides quantitative analysis tools for use with super-resolution images. MIiSR combines multiple tools for analyzing intermolecular interactions, molecular clustering and image segmentation. These tools enable quantification, in the native environment of the cell, of molecular interactions and the formation of higher-order molecular complexes. The capabilities and limitations of these analytical tools are demonstrated using both modeled data and examples derived from the vesicular trafficking system, thereby providing an established and validated experimental workflow capable of quantitatively assessing molecular interactions and molecular complex formation within the heterogeneous environment of the cell. Public Library of Science 2015-12-11 /pmc/articles/PMC4676698/ /pubmed/26657340 http://dx.doi.org/10.1371/journal.pcbi.1004634 Text en © 2015 Caetano et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Caetano, Fabiana A.
Dirk, Brennan S.
Tam, Joshua H. K.
Cavanagh, P. Craig
Goiko, Maria
Ferguson, Stephen S. G.
Pasternak, Stephen H.
Dikeakos, Jimmy D.
de Bruyn, John R.
Heit, Bryan
MIiSR: Molecular Interactions in Super-Resolution Imaging Enables the Analysis of Protein Interactions, Dynamics and Formation of Multi-protein Structures
title MIiSR: Molecular Interactions in Super-Resolution Imaging Enables the Analysis of Protein Interactions, Dynamics and Formation of Multi-protein Structures
title_full MIiSR: Molecular Interactions in Super-Resolution Imaging Enables the Analysis of Protein Interactions, Dynamics and Formation of Multi-protein Structures
title_fullStr MIiSR: Molecular Interactions in Super-Resolution Imaging Enables the Analysis of Protein Interactions, Dynamics and Formation of Multi-protein Structures
title_full_unstemmed MIiSR: Molecular Interactions in Super-Resolution Imaging Enables the Analysis of Protein Interactions, Dynamics and Formation of Multi-protein Structures
title_short MIiSR: Molecular Interactions in Super-Resolution Imaging Enables the Analysis of Protein Interactions, Dynamics and Formation of Multi-protein Structures
title_sort miisr: molecular interactions in super-resolution imaging enables the analysis of protein interactions, dynamics and formation of multi-protein structures
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676698/
https://www.ncbi.nlm.nih.gov/pubmed/26657340
http://dx.doi.org/10.1371/journal.pcbi.1004634
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