AbstractThe principal aim of this investigation was to study the change of the protein flexibility and/or conformational properties of actin filaments upon the replacement of Ca2+ by Mg2+. The temperature dependence of the fluorescence lifetime and the anisotropy decay of N-(iodoacetyl)-N′-(5-sulfo-1-naphthyl)ethylenediamine (IAEDANS) attached covalently to the Cys374 residue of actin were measured. Saturation transfer electron paramagnetic resonance (ST-EPR) experiments were also carried out using N-(1-oxyl-2,2,6,6-tetramethyl-4-piperidinyl)-maleimide (MSL) attached to the same residue (Cys374). The Arrhenius analysis of the temperature dependence of the fluorescence lifetimes shows that for Mg-F-actin, both the activation energy (E*) and ...
AbstractConformational changes in subdomain 2 of actin were investigated using fluorescence probes d...
Polymerization of actin by increasing the ionic strength leads to a quenching of almost all 1H NMR s...
AbstractPolymerization of actin by increasing the ionic strength leads to a quenching of almost all ...
AbstractThe principal aim of this investigation was to study the change of the protein flexibility a...
Temperature dependence of the fluorescence intensity and anisotropy decay of N-(iodoacetyl)-N'-(5-su...
AbstractA fluorescence resonance energy transfer (FRET) parameter, f′ (defined as the average transf...
AbstractA fluorescence resonance energy transfer (FRET) parameter, f′ (defined as the average transf...
Gln-41 on G-actin was specifically labeled with a fluorescent probe, dansyl ethylenediamine (DED), v...
G-actin has a single tight-binding (high-affinity) site for divalent cations per mole of protein, wh...
AbstractConformational changes in subdomain 2 of actin were investigated using fluorescence probes d...
AbstractFormins are conservative proteins with important roles in the regulation of the microfilamen...
AbstractIn this study, experiments were carried out in the conventional and saturation-transfer elec...
Gln-41 on G-actin was specifically labeled with a fluorescent probe, dansyl ethylenediamine (DED), v...
Polymerization of actin by increasing the ionic strength leads to a quenching of almost all 1H NMR s...
Polymerization of actin by increasing the ionic strength leads to a quenching of almost all 1H NMR s...
AbstractConformational changes in subdomain 2 of actin were investigated using fluorescence probes d...
Polymerization of actin by increasing the ionic strength leads to a quenching of almost all 1H NMR s...
AbstractPolymerization of actin by increasing the ionic strength leads to a quenching of almost all ...
AbstractThe principal aim of this investigation was to study the change of the protein flexibility a...
Temperature dependence of the fluorescence intensity and anisotropy decay of N-(iodoacetyl)-N'-(5-su...
AbstractA fluorescence resonance energy transfer (FRET) parameter, f′ (defined as the average transf...
AbstractA fluorescence resonance energy transfer (FRET) parameter, f′ (defined as the average transf...
Gln-41 on G-actin was specifically labeled with a fluorescent probe, dansyl ethylenediamine (DED), v...
G-actin has a single tight-binding (high-affinity) site for divalent cations per mole of protein, wh...
AbstractConformational changes in subdomain 2 of actin were investigated using fluorescence probes d...
AbstractFormins are conservative proteins with important roles in the regulation of the microfilamen...
AbstractIn this study, experiments were carried out in the conventional and saturation-transfer elec...
Gln-41 on G-actin was specifically labeled with a fluorescent probe, dansyl ethylenediamine (DED), v...
Polymerization of actin by increasing the ionic strength leads to a quenching of almost all 1H NMR s...
Polymerization of actin by increasing the ionic strength leads to a quenching of almost all 1H NMR s...
AbstractConformational changes in subdomain 2 of actin were investigated using fluorescence probes d...
Polymerization of actin by increasing the ionic strength leads to a quenching of almost all 1H NMR s...
AbstractPolymerization of actin by increasing the ionic strength leads to a quenching of almost all ...