Literature DB >> 28012897

Visualization of herpes simplex virus type 1 virions using fluorescent colors.

Lyns Etienne1, Poorval Joshi1, Laura Dingle1, Eugene Huang1, Peter Grzesik1, Prashant J Desai2.   

Abstract

Our laboratory was one of the first to engineer a live fluorescent tag, enhanced green fluorescent protein (eGFP), that marked the capsid of herpes simplex virus type 1 (HSV-1) and subsequently maturing virus as the particle made its way to the cell surface. In the present study we sought to increase the repertoire of colors available as fusion to the small capsid protein, VP26, so that they can be used alone or in conjunction with other fluorescent tags (fused to other HSV proteins) to follow the virus as it enters and replicates within the cell. We have now generated viruses expressing VP26 fusions with Cerulean, Venus, mOrange, tdTomato, mCherry, and Dronpa3 fluorescent proteins. These fusions were made in a repaired UL35 gene (VP26) background. These fusions do not affect the replication properties of the virus expressing the fusion polypeptide and the fusion tag was stably associated with intranuclear capsids and mature virions. Of note we could not isolate viruses expressing fusions with fluorescent proteins that have a tendency to dimerize.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Capsid; Fluorescent tags; HSV1; VP26; Venus; tdTomato

Mesh:

Substances:

Year:  2016        PMID: 28012897      PMCID: PMC5661875          DOI: 10.1016/j.jviromet.2016.12.012

Source DB:  PubMed          Journal:  J Virol Methods        ISSN: 0166-0934            Impact factor:   2.014


  35 in total

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2.  Compartmentalization of VP16 in cells infected with recombinant herpes simplex virus expressing VP16-green fluorescent protein fusion proteins.

Authors:  Sylvie La Boissière; Ander Izeta; Sophie Malcomber; Peter O'Hare
Journal:  J Virol       Date:  2004-08       Impact factor: 5.103

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4.  Green fluorescent protein as a marker for gene expression.

Authors:  M Chalfie; Y Tu; G Euskirchen; W W Ward; D C Prasher
Journal:  Science       Date:  1994-02-11       Impact factor: 47.728

5.  Fusion of a fluorescent protein to the pUL25 minor capsid protein of pseudorabies virus allows live-cell capsid imaging with negligible impact on infection.

Authors:  Kevin P Bohannon; Patricia J Sollars; Gary E Pickard; Gregory A Smith
Journal:  J Gen Virol       Date:  2011-10-05       Impact factor: 3.891

6.  Localization of herpes simplex virus type 1 UL37 in the Golgi complex requires UL36 but not capsid structures.

Authors:  Prashant Desai; Gerry L Sexton; Eugene Huang; Stanley Person
Journal:  J Virol       Date:  2008-09-10       Impact factor: 5.103

7.  The N terminus of the herpes simplex virus type 1 triplex protein, VP19C, cannot be detected on the surface of the capsid shell by using an antibody (hemagglutinin) epitope tag.

Authors:  Marieta Solé; Edward M Perkins; Augusto Frisancho; Eugene Huang; Prashant Desai
Journal:  J Virol       Date:  2007-05-23       Impact factor: 5.103

8.  Genome sequence of herpes simplex virus 1 strain KOS.

Authors:  Stuart J Macdonald; Heba H Mostafa; Lynda A Morrison; David J Davido
Journal:  J Virol       Date:  2012-06       Impact factor: 5.103

9.  Visualization of an alphaherpesvirus membrane protein that is essential for anterograde axonal spread of infection in neurons.

Authors:  M P Taylor; T Kramer; M G Lyman; R Kratchmarov; L W Enquist
Journal:  MBio       Date:  2012-05-02       Impact factor: 7.867

10.  Improper tagging of the non-essential small capsid protein VP26 impairs nuclear capsid egress of herpes simplex virus.

Authors:  Claus-Henning Nagel; Katinka Döhner; Anne Binz; Rudolf Bauerfeind; Beate Sodeik
Journal:  PLoS One       Date:  2012-08-31       Impact factor: 3.240

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Journal:  Nat Commun       Date:  2021-05-20       Impact factor: 14.919

  1 in total

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