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Connecting viral with cellular interactomes

Genome-scale screens for intraviral and virus–host protein interactions and the analysis of literature-curated datasets are able to provide a novel, comprehensive perspective of viruses, and virus-infected cells. Until now, large-scale interaction screens were predominantly performed with the yeast-...

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Detalles Bibliográficos
Autores principales: Bailer, SM, Haas, J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd. 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7108267/
https://www.ncbi.nlm.nih.gov/pubmed/19632888
http://dx.doi.org/10.1016/j.mib.2009.06.004
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author Bailer, SM
Haas, J
author_facet Bailer, SM
Haas, J
author_sort Bailer, SM
collection PubMed
description Genome-scale screens for intraviral and virus–host protein interactions and the analysis of literature-curated datasets are able to provide a novel, comprehensive perspective of viruses, and virus-infected cells. Until now, large-scale interaction screens were predominantly performed with the yeast-two-hybrid (Y2H) system; however, alternative high-throughput technologies detecting binary protein interactions or protein complexes have been developed. Although many of the previous studies suffer from a rather poor validation of the results and few biological implications, these technologies potentially lead to a plethora of novel hypotheses. Here, we will give an overview of current approaches and their technical limitations, present recent examples and novel developments.
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spelling pubmed-71082672020-03-31 Connecting viral with cellular interactomes Bailer, SM Haas, J Curr Opin Microbiol Article Genome-scale screens for intraviral and virus–host protein interactions and the analysis of literature-curated datasets are able to provide a novel, comprehensive perspective of viruses, and virus-infected cells. Until now, large-scale interaction screens were predominantly performed with the yeast-two-hybrid (Y2H) system; however, alternative high-throughput technologies detecting binary protein interactions or protein complexes have been developed. Although many of the previous studies suffer from a rather poor validation of the results and few biological implications, these technologies potentially lead to a plethora of novel hypotheses. Here, we will give an overview of current approaches and their technical limitations, present recent examples and novel developments. Published by Elsevier Ltd. 2009-08 2009-07-24 /pmc/articles/PMC7108267/ /pubmed/19632888 http://dx.doi.org/10.1016/j.mib.2009.06.004 Text en Copyright © 2009 Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Bailer, SM
Haas, J
Connecting viral with cellular interactomes
title Connecting viral with cellular interactomes
title_full Connecting viral with cellular interactomes
title_fullStr Connecting viral with cellular interactomes
title_full_unstemmed Connecting viral with cellular interactomes
title_short Connecting viral with cellular interactomes
title_sort connecting viral with cellular interactomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7108267/
https://www.ncbi.nlm.nih.gov/pubmed/19632888
http://dx.doi.org/10.1016/j.mib.2009.06.004
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