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The p12 Domain Is Unstructured in a Murine Leukemia Virus p12-CA(N) Gag Construct

The Gag polyproteins of gammaretroviruses contain a conserved p12 domain between MA and CA that plays critical roles in virus assembly, reverse transcription and nuclear integration. Here we show using nuclear magnetic resonance, that p12 is unstructured in a Moloney murine leukemia virus (MMLV) Gag...

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Detalles Bibliográficos
Autores principales: Kyere, Sampson K., Joseph, Prem Raj B., Summers, Michael F.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2277328/
https://www.ncbi.nlm.nih.gov/pubmed/18382677
http://dx.doi.org/10.1371/journal.pone.0001902
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author Kyere, Sampson K.
Joseph, Prem Raj B.
Summers, Michael F.
author_facet Kyere, Sampson K.
Joseph, Prem Raj B.
Summers, Michael F.
author_sort Kyere, Sampson K.
collection PubMed
description The Gag polyproteins of gammaretroviruses contain a conserved p12 domain between MA and CA that plays critical roles in virus assembly, reverse transcription and nuclear integration. Here we show using nuclear magnetic resonance, that p12 is unstructured in a Moloney murine leukemia virus (MMLV) Gag fragment that includes the N-terminal domain of CA (p12-CA(N)). Furthermore, no long range interactions were observed between the domains, as has been previously predicted. Flexibility appears to be a common feature of Gag “late” domains required for virus release during budding. Residues near the N-terminus of CA(N) that form a β-hairpin in the mature CA protein are unfolded in p12-CA(N), consistent with proposals that hairpin formation helps trigger capsid assembly.
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spelling pubmed-22773282008-04-02 The p12 Domain Is Unstructured in a Murine Leukemia Virus p12-CA(N) Gag Construct Kyere, Sampson K. Joseph, Prem Raj B. Summers, Michael F. PLoS One Research Article The Gag polyproteins of gammaretroviruses contain a conserved p12 domain between MA and CA that plays critical roles in virus assembly, reverse transcription and nuclear integration. Here we show using nuclear magnetic resonance, that p12 is unstructured in a Moloney murine leukemia virus (MMLV) Gag fragment that includes the N-terminal domain of CA (p12-CA(N)). Furthermore, no long range interactions were observed between the domains, as has been previously predicted. Flexibility appears to be a common feature of Gag “late” domains required for virus release during budding. Residues near the N-terminus of CA(N) that form a β-hairpin in the mature CA protein are unfolded in p12-CA(N), consistent with proposals that hairpin formation helps trigger capsid assembly. Public Library of Science 2008-04-02 /pmc/articles/PMC2277328/ /pubmed/18382677 http://dx.doi.org/10.1371/journal.pone.0001902 Text en Kyere et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kyere, Sampson K.
Joseph, Prem Raj B.
Summers, Michael F.
The p12 Domain Is Unstructured in a Murine Leukemia Virus p12-CA(N) Gag Construct
title The p12 Domain Is Unstructured in a Murine Leukemia Virus p12-CA(N) Gag Construct
title_full The p12 Domain Is Unstructured in a Murine Leukemia Virus p12-CA(N) Gag Construct
title_fullStr The p12 Domain Is Unstructured in a Murine Leukemia Virus p12-CA(N) Gag Construct
title_full_unstemmed The p12 Domain Is Unstructured in a Murine Leukemia Virus p12-CA(N) Gag Construct
title_short The p12 Domain Is Unstructured in a Murine Leukemia Virus p12-CA(N) Gag Construct
title_sort p12 domain is unstructured in a murine leukemia virus p12-ca(n) gag construct
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2277328/
https://www.ncbi.nlm.nih.gov/pubmed/18382677
http://dx.doi.org/10.1371/journal.pone.0001902
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