The fluorescence lifetime value of tryptophan residues varies by more than a factor of 100 in different proteins and is determined by several factors, which include solvent exposure and interactions with other elements of the protein matrix. Because of the variety of different elements that can alter the lifetime value and the sensitivity to the particular environment of the tryptophan residue, it is likely that non-unique lifetime values result in protein systems. The emission decay of most proteins can be satisfactorily described only using several exponential components. Here it is proposed that continuous lifetime distributions can better represent the observed decay. An approach based on protein dynamics is presented, which provides fl...
AbstractA power-like decay function, characterized by the mean excited-state lifetime and relative v...
AbstractThe Dead-End Elimination method was used to identify 40 low energy microconformations of 16 ...
The internal dynamics of human superoxide dismutase has been studied using time-resolved fluorescenc...
The fluorescence lifetime value of tryptophan residues varies by more than a factor of 100 in differ...
The fluorescence lifetime value of tryptophan residues varies by more than a factor of 100 in differ...
The decay of the tryptophanyl emission in proteins is often complex due to the sensitivity of the tr...
The decay of the tryptophanyl emission in proteins is often complex due to the sensitivity of the tr...
The picosecond time-resolved fluorescence decay data of nine single-tryptophan (trp) proteins and tw...
The picosecond time-resolved fluorescence decay data of nine single-tryptophan (trp) proteins and tw...
The analysis of the fluorescence decay using discrete exponential components assumes that a small nu...
The analysis of the fluorescence decay using discrete exponential components assumes that a small nu...
Time‐resolved fluorescence of single tryptophan proteins have demonstrated the complexity of protein...
Tryptophan fluorescence intensity decay in proteins is modeled by multiexponential functions charact...
The fluorescence intensity decay of protein is easily measurable and reports on the intrinsic fluoro...
Time-resolved fluorescence of single tryptophan proteins have demonstrated the complexity of protein...
AbstractA power-like decay function, characterized by the mean excited-state lifetime and relative v...
AbstractThe Dead-End Elimination method was used to identify 40 low energy microconformations of 16 ...
The internal dynamics of human superoxide dismutase has been studied using time-resolved fluorescenc...
The fluorescence lifetime value of tryptophan residues varies by more than a factor of 100 in differ...
The fluorescence lifetime value of tryptophan residues varies by more than a factor of 100 in differ...
The decay of the tryptophanyl emission in proteins is often complex due to the sensitivity of the tr...
The decay of the tryptophanyl emission in proteins is often complex due to the sensitivity of the tr...
The picosecond time-resolved fluorescence decay data of nine single-tryptophan (trp) proteins and tw...
The picosecond time-resolved fluorescence decay data of nine single-tryptophan (trp) proteins and tw...
The analysis of the fluorescence decay using discrete exponential components assumes that a small nu...
The analysis of the fluorescence decay using discrete exponential components assumes that a small nu...
Time‐resolved fluorescence of single tryptophan proteins have demonstrated the complexity of protein...
Tryptophan fluorescence intensity decay in proteins is modeled by multiexponential functions charact...
The fluorescence intensity decay of protein is easily measurable and reports on the intrinsic fluoro...
Time-resolved fluorescence of single tryptophan proteins have demonstrated the complexity of protein...
AbstractA power-like decay function, characterized by the mean excited-state lifetime and relative v...
AbstractThe Dead-End Elimination method was used to identify 40 low energy microconformations of 16 ...
The internal dynamics of human superoxide dismutase has been studied using time-resolved fluorescenc...