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@ARTICLE{Gensch:56498,
author = {Gensch, T. and Komolov, K. E. and Senin, I. I. and
Philippov, P. P. and Koch, K.-W.},
title = {{C}a2+-dependent conformational changes in the neuronal
{C}a2+-sensor recoverin probed by the fluorescent dye
{A}lexa647},
journal = {Proteins},
volume = {66},
issn = {0887-3585},
address = {New York, NY},
publisher = {Wiley-Liss},
reportid = {PreJuSER-56498},
pages = {492 - 499},
year = {2007},
note = {Record converted from VDB: 12.11.2012},
abstract = {Recoverin belongs to the superfamily of EF-hand
Ca2+-binding proteins and operates as a Ca2+-sensor in
vertebrate photoreceptor cells, where it regulates the
activity of rhodopsin kinase GRK1 in a Ca2+-dependent
manner. Ca2+-dependent conformational changes in recoverin
are allosterically controlled by the covalently attached
myristoyl group. The amino acid sequence of recoverin
harbors a unique cysteine at position 38. The cysteine can
be modified by the fluorescent dye Alexa647 using a
maleimide-thiol coupling step. Introduction of Alexa647 into
recoverin did not disturb the biological function of
recoverin, as it can regulate rhodopsin kinase activity like
unlabeled recoverin. Performance of the Ca2+-myristoyl
switch of labeled recoverin was monitored by Ca2+-dependent
association with immobilized lipids using surface plasmon
resonance spectroscopy. When the Ca2+-concentration was
varied, labeled myristoylated recoverin showed a
$37\%-change$ in fluorescence emission and a $34\%-change$
in excitation intensity, emission and excitation maxima
shifted by 6 and 18 nm, respectively. In contrast, labeled
nonmyristoylated recoverin exhibited only minimal changes.
Time-resolved fluorescence measurements showed
biexponentiell fluorescence decay, in which the slower time
constant of 2 ns was specifically influenced by Ca2+-induced
conformational changes. A similar influence on the slower
time constant was observed with the recoverin mutant RecE85Q
that has a disabled EF-hand 2, but no such influence was
detected with the mutant RecE121Q (EF-hand 3 is
nonfunctional) that contains the myristoyl group in a
clamped position. We conclude from our results that Alexa647
bound to cysteine 38 can monitor the conformational
transition in recoverin that is under control of the
myristoyl group.},
keywords = {Amino Acid Substitution / Animals / Calcium: pharmacology /
Calcium: physiology / Cattle / Cyclic AMP: analogs $\&$
derivatives / Cyclic AMP: chemistry / Cysteine: chemistry /
Fluorescent Dyes: chemistry / G-Protein-Coupled Receptor
Kinase 1: metabolism / Models, Molecular / Mutagenesis,
Site-Directed / Mutation, Missense / Myristic Acid:
chemistry / Point Mutation / Protein Binding / Protein
Conformation / Protein Processing, Post-Translational /
Protein Structure, Tertiary / Recombinant Fusion Proteins:
chemistry / Recoverin: chemistry / Recoverin: drug effects /
Recoverin: genetics / Spectrometry, Fluorescence /
Structure-Activity Relationship / Surface Plasmon Resonance
/ Fluorescent Dyes (NLM Chemicals) / RCV1 protein, Bos
taurus (NLM Chemicals) / Recombinant Fusion Proteins (NLM
Chemicals) / Recoverin (NLM Chemicals) / 8-aminohexylamino
cAMP (NLM Chemicals) / Cysteine (NLM Chemicals) / Myristic
Acid (NLM Chemicals) / Cyclic AMP (NLM Chemicals) / Calcium
(NLM Chemicals) / G-Protein-Coupled Receptor Kinase 1 (NLM
Chemicals) / J (WoSType)},
cin = {INB-1},
ddc = {540},
cid = {I:(DE-Juel1)VDB804},
pnm = {Funktion und Dysfunktion des Nervensystems},
pid = {G:(DE-Juel1)FUEK409},
shelfmark = {Biochemistry $\&$ Molecular Biology / Biophysics},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:17078090},
UT = {WOS:000243358000018},
doi = {10.1002/prot.21231},
url = {https://juser.fz-juelich.de/record/56498},
}