| Abstract: | A series of four bovine pancreatic trypsin inhibitor (BPTI) derivatives, site specifically labeled by (2-methoxy-1-naphthyl)methyl (MNA) at the N-terminal amino group and by [7-(dimethylamino)-coumarin-4-yl]acetyl (DA-coum) at one of the four epsilon-amino groups, was prepared. The four derivatives, N alpha-MNA-Arg1-N epsilon-DA-coum-Lysn-BPTI [(1-n)BPTI] (n = 15, 26, 41, and 46), were purified by affinity chromatography and high-performance liquid chromatography (HPLC). The homogeneity of each derivative and its site of labeling were characterized by HPLC tryptic peptide mapping. Nonradiative energy transfer from MNA (donor) to DA-coum (acceptor) was measured by monitoring donor emission and acceptor excitation spectra. Transfer efficiencies between 45% and 85% were observed. The fluorescence decay of MNA in MNA-BPTI, a derivative labeled by a donor without an acceptor, is monoexponential, with a lifetime of 6.8 +/- 0.15 ns. The decay kinetics of MNA fluorescence measured for derivatives labeled both by donor and acceptor showed a small deviation from monoexponential decay with shorter average lifetimes. Analysis of the experimental decay curves yielded the detailed intramolecular distance distribution functions for each pair of labeled sites. The averages of the calculated distance distribution functions are close to the values expected from the known structure of BPTI in the crystalline state. The derivatives thus obtained are suitable for investigation of conformational transitions of the labeled protein and for monitoring localized changes such as those involved in the folding or unfolding transitions. |
