Measurement Of Interpeptidic Cu-Ii Exchange Rate Constants Of Cu-Ii-Amyloid-Beta Complexes To Small Peptide Motifs By Tryptophan Fluorescence Quenching

The interpeptidic Cu-II exchange rate constants were measured for two Cu amyloid-beta complexes, Cu(A beta(1-16)) and Cu(A beta(1-28)), to fluorescent peptides GHW and DAHW using a quantitative tryptophan fluorescence quenching methodology. The second-order rate constants were determined at three pH values (6.8, 7.4, and 8.7) important to the two Cu(A beta) coordination complexes, components Cu(A beta)(I) and Cu(A beta)(II). The interpeptidic Cu-II exchange rate constant is approximately 10(4) M-1 s(-1 )but varies in magnitude depending on many variables. These include pH, length of the A beta peptide, location of the anchoring histidine ligand in the fluorescent peptide, number of amide deprotonations required in the tryptophan peptide to coordinate Cu-II, and interconversion between Cu(A beta)(I) and Cu(A beta)(II). We also present EPR data probing the Cu-II exchange between peptides and the formation of ternary species between Cu(A beta) and GHW. As the nonfluorescent GHK and DAHK peptides are important motifs found in the blood and serum, their ability to sequester Cu-II ions from Cu(A beta) complexes may be relevant for the metal homeostasis and its implication in Alzheimer's disease. Thus, their kinetic Cu-II interpeptidic exchange rate constants are important chemical rate constants that can help elucidate the complex Cu-II trafficking puzzle in the synaptic cleft.