AbstractRibonuclease Sa (RNase Sa) contains no tryptophan (Trp) residues. We have added single Trp residues to RNase Sa at sites where Trp is found in four other microbial ribonucleases, yielding the following variants of RNase Sa: Y52W, Y55W, T76W, and Y81W. We have determined crystal structures of T76W and Y81W at 1.1 and 1.0Å resolution, respectively. We have studied the fluorescence properties and stabilities of the four variants and compared them to wild-type RNase Sa and the other ribonucleases on which they were based. Our results should help others in selecting sites for adding Trp residues to proteins. The most interesting findings are: 1), Y52W is 2.9kcal/mol less stable than RNase Sa and the fluorescence intensity emission maximu...
Time correlated single photon counting measurements of tryptophan (Trp) fluorescence intensity decay...
The fluorescence decay properties of wild-type trp repressor (TR) have been characterized by carryin...
The primary objective was to study the kinetics of folding of RNase Sa. Wild-type RNase Sa does not...
AbstractRibonuclease Sa (RNase Sa) contains no tryptophan (Trp) residues. We have added single Trp r...
AbstractThis article probes the denatured state ensemble of ribonuclease Sa (RNase Sa) using fluores...
AbstractCharacterizing the denatured state ensemble is crucial to understanding protein stability an...
Vita.Site-directed mutagenesis was used to examine the contribution of buried and exposed aromatic a...
The interactions of tryptophan-59 (TRP-59) and its protein environment in ribonuclease-T1 (RNAse-T1)...
To understand protein stability and the mechanism of protein folding, it is essential that we gain a...
The tryptophyl fluorescence of ribonuclease T1 decays monoexponentially at pH 5.5, tau = 4.04 ns but...
Fluorescence spectroscopy can reveal insights into the structure, function and dynamics of proteins ...
Although relatively rare, the tryptophan residue (Trp), with its large hydrophobic surface, has a un...
AbstractThe origin of the biexponential fluorescence decay of Trp in ribonuclease T1 under mildly de...
The local environments of the four tryptophan residues of the extracellular domain of human tissue f...
Molecular dynamics simulations of Ribonuclease-T1 (RNAse-T1) were performed using x-ray crystal coor...
Time correlated single photon counting measurements of tryptophan (Trp) fluorescence intensity decay...
The fluorescence decay properties of wild-type trp repressor (TR) have been characterized by carryin...
The primary objective was to study the kinetics of folding of RNase Sa. Wild-type RNase Sa does not...
AbstractRibonuclease Sa (RNase Sa) contains no tryptophan (Trp) residues. We have added single Trp r...
AbstractThis article probes the denatured state ensemble of ribonuclease Sa (RNase Sa) using fluores...
AbstractCharacterizing the denatured state ensemble is crucial to understanding protein stability an...
Vita.Site-directed mutagenesis was used to examine the contribution of buried and exposed aromatic a...
The interactions of tryptophan-59 (TRP-59) and its protein environment in ribonuclease-T1 (RNAse-T1)...
To understand protein stability and the mechanism of protein folding, it is essential that we gain a...
The tryptophyl fluorescence of ribonuclease T1 decays monoexponentially at pH 5.5, tau = 4.04 ns but...
Fluorescence spectroscopy can reveal insights into the structure, function and dynamics of proteins ...
Although relatively rare, the tryptophan residue (Trp), with its large hydrophobic surface, has a un...
AbstractThe origin of the biexponential fluorescence decay of Trp in ribonuclease T1 under mildly de...
The local environments of the four tryptophan residues of the extracellular domain of human tissue f...
Molecular dynamics simulations of Ribonuclease-T1 (RNAse-T1) were performed using x-ray crystal coor...
Time correlated single photon counting measurements of tryptophan (Trp) fluorescence intensity decay...
The fluorescence decay properties of wild-type trp repressor (TR) have been characterized by carryin...
The primary objective was to study the kinetics of folding of RNase Sa. Wild-type RNase Sa does not...