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      Superresolution Imaging of Human Cytomegalovirus vMIA Localization in Sub-Mitochondrial Compartments

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          Abstract

          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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          Most cited references61

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          NIH Image to ImageJ: 25 years of image analysis.

          For the past 25 years NIH Image and ImageJ software have been pioneers as open tools for the analysis of scientific images. We discuss the origins, challenges and solutions of these two programs, and how their history can serve to advise and inform other software projects.
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            Far-field optical nanoscopy.

            In 1873, Ernst Abbe discovered what was to become a well-known paradigm: the inability of a lens-based optical microscope to discern details that are closer together than half of the wavelength of light. However, for its most popular imaging mode, fluorescence microscopy, the diffraction barrier is crumbling. Here, I discuss the physical concepts that have pushed fluorescence microscopy to the nanoscale, once the prerogative of electron and scanning probe microscopes. Initial applications indicate that emergent far-field optical nanoscopy will have a strong impact in the life sciences and in other areas benefiting from nanoscale visualization.
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              Computer control of microscopes using µManager.

              With the advent of digital cameras and motorization of mechanical components, computer control of microscopes has become increasingly important. Software for microscope image acquisition should not only be easy to use, but also enable and encourage novel approaches. The open-source software package µManager aims to fulfill those goals. This unit provides step-by-step protocols describing how to get started working with µManager, as well as some starting points for advanced use of the software. © 2010 by John Wiley & Sons, Inc.
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                Author and article information

                Journal
                Viruses
                Viruses
                viruses
                Viruses
                MDPI
                1999-4915
                09 April 2014
                April 2014
                : 6
                : 4
                : 1612-1636
                Affiliations
                [1 ]Research Center for Genetic Medicine, Children’s Research Institute, Children’s National Health System, 111 Michigan Avenue, NW, Washington, DC 20010, USA; E-Mails: SBhuvanendran@ 123456childrensnational.org (S.B.); kyle.salka@ 123456gmail.com (K.S.); Sreetama.SenChandra@ 123456childrensnational.org (S.C.S.); elizabeth.anne.williams.umd@ 123456gmail.com (E.W.); maggie.leeker@ 123456gmail.com (M.L.); VPrasad@ 123456childrensnational.org (V.P.)
                [2 ]Section on Biophotonics, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, MD 20892, USA; E-Mail: kristin.rainey@ 123456nih.gov
                [3 ]Life Science Division, Leica Microsystems, Inc., 1700 Leider Lane, Buffalo Grove, IL 60089, USA; E-Mail: Jonathan.Boyd@ 123456Leica-Microsystems.com
                [4 ]Department of Integrative Systems Biology, George Washington University School of Medicine and Health Sciences, Washington, DC 20037, USA
                [5 ]Department of Biochemistry and Molecular Medicine, George Washington University School of Medicine and Health Sciences, Washington, DC 20037, USA
                Author notes
                [* ]Authors to whom correspondence should be addressed; E-Mails: pattersg@ 123456mail.nih.gov (G.H.P.); jkjaiswal@ 123456childrensnational.org (J.K.J.); acolberg-poley@ 123456childrensnational.org (A.M.C.-P.); Tel.: +1-202-476-3984 (A.M.C.-P.); Fax: +1-202-476-6014 (A.M.C.-P.).
                Article
                viruses-06-01612
                10.3390/v6041612
                4014713
                24721787
                4aa978ed-7028-40b5-ad93-2d8044f52c6f
                © 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/).

                History
                : 17 January 2014
                : 16 March 2014
                : 27 March 2014
                Categories
                Article

                Microbiology & Virology
                hcmv vmia,mam,mitochondria,omm,matrix,confocal microscopy,superresolution microscopy,gsted,msim,palm

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