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Molecular dynamics simulations reveal that AEDANS is an inert fluorescent probe for the study of membrane proteins

Computer simulations were carried out of a number of AEDANS-labeled single cysteine mutants of a small reference membrane protein, M13 major coat protein, covering 60% of its primary sequence. M13 major coat protein is a single membrane-spanning, α-helical membrane protein with a relatively large wa...

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Autores principales: Vos, Werner L., Schor, Marieke, Baumgaertner, Artur, Tieleman, D. Peter, Hemminga, Marcus A.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795155/
https://www.ncbi.nlm.nih.gov/pubmed/19669748
http://dx.doi.org/10.1007/s00249-009-0527-9
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author Vos, Werner L.
Schor, Marieke
Baumgaertner, Artur
Tieleman, D. Peter
Hemminga, Marcus A.
author_facet Vos, Werner L.
Schor, Marieke
Baumgaertner, Artur
Tieleman, D. Peter
Hemminga, Marcus A.
author_sort Vos, Werner L.
collection PubMed
description Computer simulations were carried out of a number of AEDANS-labeled single cysteine mutants of a small reference membrane protein, M13 major coat protein, covering 60% of its primary sequence. M13 major coat protein is a single membrane-spanning, α-helical membrane protein with a relatively large water-exposed region in the N-terminus. In 10-ns molecular dynamics simulations, we analyze the behavior of the AEDANS label and the native tryptophan, which were used as acceptor and donor in previous FRET experiments. The results indicate that AEDANS is a relatively inert environmental probe that can move unhindered through the lipid membrane when attached to a membrane protein.
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spelling pubmed-27951552009-12-23 Molecular dynamics simulations reveal that AEDANS is an inert fluorescent probe for the study of membrane proteins Vos, Werner L. Schor, Marieke Baumgaertner, Artur Tieleman, D. Peter Hemminga, Marcus A. Eur Biophys J Original Paper Computer simulations were carried out of a number of AEDANS-labeled single cysteine mutants of a small reference membrane protein, M13 major coat protein, covering 60% of its primary sequence. M13 major coat protein is a single membrane-spanning, α-helical membrane protein with a relatively large water-exposed region in the N-terminus. In 10-ns molecular dynamics simulations, we analyze the behavior of the AEDANS label and the native tryptophan, which were used as acceptor and donor in previous FRET experiments. The results indicate that AEDANS is a relatively inert environmental probe that can move unhindered through the lipid membrane when attached to a membrane protein. Springer-Verlag 2009-08-11 2010 /pmc/articles/PMC2795155/ /pubmed/19669748 http://dx.doi.org/10.1007/s00249-009-0527-9 Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
Vos, Werner L.
Schor, Marieke
Baumgaertner, Artur
Tieleman, D. Peter
Hemminga, Marcus A.
Molecular dynamics simulations reveal that AEDANS is an inert fluorescent probe for the study of membrane proteins
title Molecular dynamics simulations reveal that AEDANS is an inert fluorescent probe for the study of membrane proteins
title_full Molecular dynamics simulations reveal that AEDANS is an inert fluorescent probe for the study of membrane proteins
title_fullStr Molecular dynamics simulations reveal that AEDANS is an inert fluorescent probe for the study of membrane proteins
title_full_unstemmed Molecular dynamics simulations reveal that AEDANS is an inert fluorescent probe for the study of membrane proteins
title_short Molecular dynamics simulations reveal that AEDANS is an inert fluorescent probe for the study of membrane proteins
title_sort molecular dynamics simulations reveal that aedans is an inert fluorescent probe for the study of membrane proteins
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795155/
https://www.ncbi.nlm.nih.gov/pubmed/19669748
http://dx.doi.org/10.1007/s00249-009-0527-9
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