Real time observation of single membrane protein insertion events by the Escherichia coli insertase YidC.
Membrane protein translocation and insertion is a central issue in biology. Here we focus on a minimal system, the membrane insertase YidC of Escherichia coli that inserts small proteins into the cytoplasmic membrane. In a reconstituted system individual insertion processes were followed by single-p...
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doaj-59c49eee6bfe444dbaab429205cb3e192020-11-25T02:42:34ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5902310.1371/journal.pone.0059023Real time observation of single membrane protein insertion events by the Escherichia coli insertase YidC.Sophie WinterfeldStefan ErnstMichael BörschUwe GerkenAndreas KuhnMembrane protein translocation and insertion is a central issue in biology. Here we focus on a minimal system, the membrane insertase YidC of Escherichia coli that inserts small proteins into the cytoplasmic membrane. In a reconstituted system individual insertion processes were followed by single-pair fluorescence resonance energy transfer (FRET), with a pair of fluorophores on YidC and the substrate Pf3 coat protein. After addition of N-terminally labeled Pf3 coat protein a close contact to YidC at its cytoplasmic label was observed. This allowed to monitor the translocation of the N-terminal domain of Pf3 coat protein across the membrane in real time. Translocation occurred within milliseconds as the label on the N-terminal domain rapidly approached the fluorophore on the periplasmic domain of YidC at the trans side of the membrane. After the close contact, the two fluorophores separated, reflecting the release of the translocated Pf3 coat protein from YidC into the membrane bilayer. When the Pf3 coat protein was labeled C-terminally, no translocation of the label was observed although efficient binding to the cytoplasmic positions of YidC occurred.http://europepmc.org/articles/PMC3602594?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sophie Winterfeld Stefan Ernst Michael Börsch Uwe Gerken Andreas Kuhn |
spellingShingle |
Sophie Winterfeld Stefan Ernst Michael Börsch Uwe Gerken Andreas Kuhn Real time observation of single membrane protein insertion events by the Escherichia coli insertase YidC. PLoS ONE |
author_facet |
Sophie Winterfeld Stefan Ernst Michael Börsch Uwe Gerken Andreas Kuhn |
author_sort |
Sophie Winterfeld |
title |
Real time observation of single membrane protein insertion events by the Escherichia coli insertase YidC. |
title_short |
Real time observation of single membrane protein insertion events by the Escherichia coli insertase YidC. |
title_full |
Real time observation of single membrane protein insertion events by the Escherichia coli insertase YidC. |
title_fullStr |
Real time observation of single membrane protein insertion events by the Escherichia coli insertase YidC. |
title_full_unstemmed |
Real time observation of single membrane protein insertion events by the Escherichia coli insertase YidC. |
title_sort |
real time observation of single membrane protein insertion events by the escherichia coli insertase yidc. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2013-01-01 |
description |
Membrane protein translocation and insertion is a central issue in biology. Here we focus on a minimal system, the membrane insertase YidC of Escherichia coli that inserts small proteins into the cytoplasmic membrane. In a reconstituted system individual insertion processes were followed by single-pair fluorescence resonance energy transfer (FRET), with a pair of fluorophores on YidC and the substrate Pf3 coat protein. After addition of N-terminally labeled Pf3 coat protein a close contact to YidC at its cytoplasmic label was observed. This allowed to monitor the translocation of the N-terminal domain of Pf3 coat protein across the membrane in real time. Translocation occurred within milliseconds as the label on the N-terminal domain rapidly approached the fluorophore on the periplasmic domain of YidC at the trans side of the membrane. After the close contact, the two fluorophores separated, reflecting the release of the translocated Pf3 coat protein from YidC into the membrane bilayer. When the Pf3 coat protein was labeled C-terminally, no translocation of the label was observed although efficient binding to the cytoplasmic positions of YidC occurred. |
url |
http://europepmc.org/articles/PMC3602594?pdf=render |
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