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Superresolution Imaging of Human Cytomegalovirus vMIA Localization in Sub-Mitochondrial Compartments
The human cytomegalovirus (HCMV) viral mitochondria-localized inhibitor of apoptosis (vMIA) protein, traffics to mitochondria-associated membranes (MAM), where the endoplasmic reticulum (ER) contacts the outer mitochondrial membrane (OMM). vMIA association with the MAM has not been visualized by ima...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014713/ https://www.ncbi.nlm.nih.gov/pubmed/24721787 http://dx.doi.org/10.3390/v6041612 |
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author | Bhuvanendran, Shivaprasad Salka, Kyle Rainey, Kristin Sreetama, Sen Chandra Williams, Elizabeth Leeker, Margretha Prasad, Vidhya Boyd, Jonathan Patterson, George H. Jaiswal, Jyoti K. Colberg-Poley, Anamaris M. |
author_facet | Bhuvanendran, Shivaprasad Salka, Kyle Rainey, Kristin Sreetama, Sen Chandra Williams, Elizabeth Leeker, Margretha Prasad, Vidhya Boyd, Jonathan Patterson, George H. Jaiswal, Jyoti K. Colberg-Poley, Anamaris M. |
author_sort | Bhuvanendran, Shivaprasad |
collection | PubMed |
description | The human cytomegalovirus (HCMV) viral mitochondria-localized inhibitor of apoptosis (vMIA) protein, traffics to mitochondria-associated membranes (MAM), where the endoplasmic reticulum (ER) contacts the outer mitochondrial membrane (OMM). vMIA association with the MAM has not been visualized by imaging. Here, we have visualized this by using a combination of confocal and superresolution imaging. Deconvolution of confocal microscopy images shows vMIA localizes away from mitochondrial matrix at the Mitochondria-ER interface. By gated stimulated emission depletion (GSTED) imaging, we show that along this interface vMIA is distributed in clusters. Through multicolor, multifocal structured illumination microscopy (MSIM), we find vMIA clusters localize away from MitoTracker Red, indicating its OMM localization. GSTED and MSIM imaging show vMIA exists in clusters of ~100–150 nm, which is consistent with the cluster size determined by Photoactivated Localization Microscopy (PALM). With these diverse superresolution approaches, we have imaged the clustered distribution of vMIA at the OMM adjacent to the ER. Our findings directly compare the relative advantages of each of these superresolution imaging modalities for imaging components of the MAM and sub-mitochondrial compartments. These studies establish the ability of superresolution imaging to provide valuable insight into viral protein location, particularly in the sub-mitochondrial compartments, and into their clustered organization. |
format | Online Article Text |
id | pubmed-4014713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-40147132014-05-09 Superresolution Imaging of Human Cytomegalovirus vMIA Localization in Sub-Mitochondrial Compartments Bhuvanendran, Shivaprasad Salka, Kyle Rainey, Kristin Sreetama, Sen Chandra Williams, Elizabeth Leeker, Margretha Prasad, Vidhya Boyd, Jonathan Patterson, George H. Jaiswal, Jyoti K. Colberg-Poley, Anamaris M. Viruses Article The human cytomegalovirus (HCMV) viral mitochondria-localized inhibitor of apoptosis (vMIA) protein, traffics to mitochondria-associated membranes (MAM), where the endoplasmic reticulum (ER) contacts the outer mitochondrial membrane (OMM). vMIA association with the MAM has not been visualized by imaging. Here, we have visualized this by using a combination of confocal and superresolution imaging. Deconvolution of confocal microscopy images shows vMIA localizes away from mitochondrial matrix at the Mitochondria-ER interface. By gated stimulated emission depletion (GSTED) imaging, we show that along this interface vMIA is distributed in clusters. Through multicolor, multifocal structured illumination microscopy (MSIM), we find vMIA clusters localize away from MitoTracker Red, indicating its OMM localization. GSTED and MSIM imaging show vMIA exists in clusters of ~100–150 nm, which is consistent with the cluster size determined by Photoactivated Localization Microscopy (PALM). With these diverse superresolution approaches, we have imaged the clustered distribution of vMIA at the OMM adjacent to the ER. Our findings directly compare the relative advantages of each of these superresolution imaging modalities for imaging components of the MAM and sub-mitochondrial compartments. These studies establish the ability of superresolution imaging to provide valuable insight into viral protein location, particularly in the sub-mitochondrial compartments, and into their clustered organization. MDPI 2014-04-09 /pmc/articles/PMC4014713/ /pubmed/24721787 http://dx.doi.org/10.3390/v6041612 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Bhuvanendran, Shivaprasad Salka, Kyle Rainey, Kristin Sreetama, Sen Chandra Williams, Elizabeth Leeker, Margretha Prasad, Vidhya Boyd, Jonathan Patterson, George H. Jaiswal, Jyoti K. Colberg-Poley, Anamaris M. Superresolution Imaging of Human Cytomegalovirus vMIA Localization in Sub-Mitochondrial Compartments |
title | Superresolution Imaging of Human Cytomegalovirus vMIA Localization in Sub-Mitochondrial Compartments |
title_full | Superresolution Imaging of Human Cytomegalovirus vMIA Localization in Sub-Mitochondrial Compartments |
title_fullStr | Superresolution Imaging of Human Cytomegalovirus vMIA Localization in Sub-Mitochondrial Compartments |
title_full_unstemmed | Superresolution Imaging of Human Cytomegalovirus vMIA Localization in Sub-Mitochondrial Compartments |
title_short | Superresolution Imaging of Human Cytomegalovirus vMIA Localization in Sub-Mitochondrial Compartments |
title_sort | superresolution imaging of human cytomegalovirus vmia localization in sub-mitochondrial compartments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014713/ https://www.ncbi.nlm.nih.gov/pubmed/24721787 http://dx.doi.org/10.3390/v6041612 |
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