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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Main Authors: Sophie Winterfeld, Stefan Ernst, Michael Börsch, Uwe Gerken, Andreas Kuhn
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3602594?pdf=render
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spelling 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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