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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
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.
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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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