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

被引:4
|
作者
Vos, Werner L. [1 ]
Schor, Marieke [1 ]
Baumgaertner, Artur [2 ]
Tieleman, D. Peter [3 ]
Hemminga, Marcus A. [1 ]
机构
[1] Wageningen Univ, Biophys Lab, NL-6700 ET Wageningen, Netherlands
[2] Forschungszentrum, Inst Festkorperforsch, D-5170 Julich, Germany
[3] Univ Calgary, Dept Biol Sci, Calgary, AB T2N 1N4, Canada
来源
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS | 2010年 / 39卷 / 02期
关键词
Membrane proteins; Side-chain conformations; Tryptophan; Energy transfer (FRET); Computer simulation; MAJOR COAT PROTEIN; TRANSMEMBRANE ALPHA-HELIX; ENERGY-TRANSFER; FRET; ORIENTATION; CONFORMATION; MODEL; SPECTRA; BILAYER; CHANNEL;
D O I
10.1007/s00249-009-0527-9
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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, alpha-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.
引用
收藏
页码:229 / 239
页数:11
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