<p>Fluorescence emission intensity is of donor (A488) at 515 nm with excitation at 450 nm. Fluorescence of native protein is determined at 0.1 M GuHCl (i.e., at the lowest concentration denaturant used), whereas fluorescence of unfolded protein is determined at 6.9 M GuHCl.</p
Fluorescence spectroscopy is an important tool for the characterization of protein folding. Often, a...
<p>Spectral centers of mass of the intrinsic fluorescence emission of apoA-I are plotted as a functi...
<p>The dye-protein conjugates (AF555-R141H 0.15 mg/ml, AF488-F119L 0.26 mg/ml) were analyzed by UV-s...
<p>Shown are fluorescence data of ‘donor-only’ protein (open circles), d69-a1 (blue circles), d69-a1...
Uniform labeling of proteins with fluorescent donor and acceptor dyes with an equimolar ratio is par...
Uniform labeling of proteins with fluorescent donor and acceptor dyes with an equimolar ratio is par...
Uniform labeling of proteins with fluorescent donor and acceptor dyes with an equimolar ratio is par...
Abstract: Uniform labeling of proteins with fluorescent donor and acceptor dyes with an equimolar ra...
<p>(a) Normalized emission spectra of ‘donor-only’ apoflavodoxin. The inset zooms in on the fluoresc...
<p>(A) Fluorescence emission intensity of A488 at 515 nm upon excitation at 475 nm. (B) Fluorescence...
<p><a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0045746#pone.0045746-Bollen...
<p>(A) Denaturant dependence of A488 fluorescence <i>F</i>. A488 is excited at its denaturant-depend...
<p>In all protein variants, donor label (i.e., A488) is attached to residue 69. (a) Positions of dye...
<p><b>A</b>) Fluorescence emission spectra of 10 nM PA<sup>E733C*AF488</sup> (solid line; donor alon...
Fluorescence spectroscopy is an important tool for the characterization of protein folding. Often, a...
Fluorescence spectroscopy is an important tool for the characterization of protein folding. Often, a...
<p>Spectral centers of mass of the intrinsic fluorescence emission of apoA-I are plotted as a functi...
<p>The dye-protein conjugates (AF555-R141H 0.15 mg/ml, AF488-F119L 0.26 mg/ml) were analyzed by UV-s...
<p>Shown are fluorescence data of ‘donor-only’ protein (open circles), d69-a1 (blue circles), d69-a1...
Uniform labeling of proteins with fluorescent donor and acceptor dyes with an equimolar ratio is par...
Uniform labeling of proteins with fluorescent donor and acceptor dyes with an equimolar ratio is par...
Uniform labeling of proteins with fluorescent donor and acceptor dyes with an equimolar ratio is par...
Abstract: Uniform labeling of proteins with fluorescent donor and acceptor dyes with an equimolar ra...
<p>(a) Normalized emission spectra of ‘donor-only’ apoflavodoxin. The inset zooms in on the fluoresc...
<p>(A) Fluorescence emission intensity of A488 at 515 nm upon excitation at 475 nm. (B) Fluorescence...
<p><a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0045746#pone.0045746-Bollen...
<p>(A) Denaturant dependence of A488 fluorescence <i>F</i>. A488 is excited at its denaturant-depend...
<p>In all protein variants, donor label (i.e., A488) is attached to residue 69. (a) Positions of dye...
<p><b>A</b>) Fluorescence emission spectra of 10 nM PA<sup>E733C*AF488</sup> (solid line; donor alon...
Fluorescence spectroscopy is an important tool for the characterization of protein folding. Often, a...
Fluorescence spectroscopy is an important tool for the characterization of protein folding. Often, a...
<p>Spectral centers of mass of the intrinsic fluorescence emission of apoA-I are plotted as a functi...
<p>The dye-protein conjugates (AF555-R141H 0.15 mg/ml, AF488-F119L 0.26 mg/ml) were analyzed by UV-s...