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Shigella flexneri Spa15 Crystal Structure Verified in Solution by Double Electron Electron Resonance
Shigella flexneri Spa15 is a chaperone of the type 3 secretion system, which binds a number of effectors to ensure their stabilization prior to secretion. One of these effectors is IpgB1, a mimic of the human Ras-like Rho guanosine triphosphatase RhoG. In this study, Spa15 alone and in complex with...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021122/ https://www.ncbi.nlm.nih.gov/pubmed/21075116 http://dx.doi.org/10.1016/j.jmb.2010.10.053 |
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author | Lillington, James E.D. Lovett, Janet E. Johnson, Steven Roversi, Pietro Timmel, Christiane R. Lea, Susan M. |
author_facet | Lillington, James E.D. Lovett, Janet E. Johnson, Steven Roversi, Pietro Timmel, Christiane R. Lea, Susan M. |
author_sort | Lillington, James E.D. |
collection | PubMed |
description | Shigella flexneri Spa15 is a chaperone of the type 3 secretion system, which binds a number of effectors to ensure their stabilization prior to secretion. One of these effectors is IpgB1, a mimic of the human Ras-like Rho guanosine triphosphatase RhoG. In this study, Spa15 alone and in complex with IpgB1 has been studied by double electron electron resonance, an experiment that gives distance information showing the spacial separation of attached spin labels. This distance is explained by determining the crystal structure of the spin-labeled Spa15 where labels are seen to be buried in hydrophobic pockets. The double electron electron resonance experiment on the Spa15 complex with IpgB1 shows that IpgB1 does not bind Spa15 in the same way as is seen in the homologous Salmonella sp. chaperone:effector complex InvB:SipA. |
format | Text |
id | pubmed-3021122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-30211222011-02-11 Shigella flexneri Spa15 Crystal Structure Verified in Solution by Double Electron Electron Resonance Lillington, James E.D. Lovett, Janet E. Johnson, Steven Roversi, Pietro Timmel, Christiane R. Lea, Susan M. J Mol Biol Article Shigella flexneri Spa15 is a chaperone of the type 3 secretion system, which binds a number of effectors to ensure their stabilization prior to secretion. One of these effectors is IpgB1, a mimic of the human Ras-like Rho guanosine triphosphatase RhoG. In this study, Spa15 alone and in complex with IpgB1 has been studied by double electron electron resonance, an experiment that gives distance information showing the spacial separation of attached spin labels. This distance is explained by determining the crystal structure of the spin-labeled Spa15 where labels are seen to be buried in hydrophobic pockets. The double electron electron resonance experiment on the Spa15 complex with IpgB1 shows that IpgB1 does not bind Spa15 in the same way as is seen in the homologous Salmonella sp. chaperone:effector complex InvB:SipA. Elsevier 2011-01-14 /pmc/articles/PMC3021122/ /pubmed/21075116 http://dx.doi.org/10.1016/j.jmb.2010.10.053 Text en © 2011 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Lillington, James E.D. Lovett, Janet E. Johnson, Steven Roversi, Pietro Timmel, Christiane R. Lea, Susan M. Shigella flexneri Spa15 Crystal Structure Verified in Solution by Double Electron Electron Resonance |
title | Shigella flexneri Spa15 Crystal Structure Verified in Solution by Double Electron Electron Resonance |
title_full | Shigella flexneri Spa15 Crystal Structure Verified in Solution by Double Electron Electron Resonance |
title_fullStr | Shigella flexneri Spa15 Crystal Structure Verified in Solution by Double Electron Electron Resonance |
title_full_unstemmed | Shigella flexneri Spa15 Crystal Structure Verified in Solution by Double Electron Electron Resonance |
title_short | Shigella flexneri Spa15 Crystal Structure Verified in Solution by Double Electron Electron Resonance |
title_sort | shigella flexneri spa15 crystal structure verified in solution by double electron electron resonance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021122/ https://www.ncbi.nlm.nih.gov/pubmed/21075116 http://dx.doi.org/10.1016/j.jmb.2010.10.053 |
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