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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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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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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. |
format | Text |
id | pubmed-2277328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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