Intrinsically disordered protein regions and many other biopolymers lack the three-dimensional structure that could be determined by X-ray crystallography or NMR, which encourages the application of alternative experimental methods. Time-resolved resonance energy transfer data are often used to measure distances between two fluorophores attached to a flexible biopolymer. This is complicated by the rotational and translational diffusion of the fluorophores and by nonmonoexponential donor decay in the absence of the acceptor. Equation <i>I</i><sub>DA</sub>(<i>t</i>) = <i>I</i><sub>D</sub>(<i>t</i>)·<i>F</i>(<i>t</i>) is derived here, which is applicable regardless of whether <i>I</i><sub>D</sub>(<i>t</i>) is monoexponential. <i>I</i><sub>D</s...
Fluorescence resonance energy transfer (FRET) is routinely used to study equilibrium and dynamical p...
Fluorescence resonance energy transfer (FRET) is routinely used to study equilibrium and dynamical p...
Intramolecular distances in proteins and other biomolecules can be studied in living cells by means ...
The structural and dynamic properties of a flexible peptidic chain codetermine its biological activi...
A flexible peptide chain displays structural and dynamic properties that correspond to its folding a...
A flexible peptide chain displays structural and dynamic properties that correspond to its folding a...
Fluorescence energy transfer is widely used for determination of intramolecular distances in macromo...
Fluorescence resonance energy transfer (FRET) is a popular tool to study equilibrium and dynamical p...
Fluorescence resonance energy transfer (FRET) is a popular tool to study equilibrium and dynamical p...
Most active biopolymers are dynamic structures; thus, ensembles of such molecules should be characte...
Förster resonance energy transfer (FRET) allows in principal for the structural changes of biologica...
Fluorescence resonance energy transfer (FRET) is a popular tool to study equilibrium and dynamical p...
Förster resonance energy transfer (FRET) is a widely used single-molecule technique for measuring na...
Fluorescence resonance energy transfer (FRET) is a popular tool to study equilibrium and dynamical p...
Two recently developed theories of electronic energy transfer/migration were for the first time appl...
Fluorescence resonance energy transfer (FRET) is routinely used to study equilibrium and dynamical p...
Fluorescence resonance energy transfer (FRET) is routinely used to study equilibrium and dynamical p...
Intramolecular distances in proteins and other biomolecules can be studied in living cells by means ...
The structural and dynamic properties of a flexible peptidic chain codetermine its biological activi...
A flexible peptide chain displays structural and dynamic properties that correspond to its folding a...
A flexible peptide chain displays structural and dynamic properties that correspond to its folding a...
Fluorescence energy transfer is widely used for determination of intramolecular distances in macromo...
Fluorescence resonance energy transfer (FRET) is a popular tool to study equilibrium and dynamical p...
Fluorescence resonance energy transfer (FRET) is a popular tool to study equilibrium and dynamical p...
Most active biopolymers are dynamic structures; thus, ensembles of such molecules should be characte...
Förster resonance energy transfer (FRET) allows in principal for the structural changes of biologica...
Fluorescence resonance energy transfer (FRET) is a popular tool to study equilibrium and dynamical p...
Förster resonance energy transfer (FRET) is a widely used single-molecule technique for measuring na...
Fluorescence resonance energy transfer (FRET) is a popular tool to study equilibrium and dynamical p...
Two recently developed theories of electronic energy transfer/migration were for the first time appl...
Fluorescence resonance energy transfer (FRET) is routinely used to study equilibrium and dynamical p...
Fluorescence resonance energy transfer (FRET) is routinely used to study equilibrium and dynamical p...
Intramolecular distances in proteins and other biomolecules can be studied in living cells by means ...