13C Nuclear Magnetic Resonance and Circular Dichroism Studies of the Tuftsin Conformation in Water

Abstract
13C-NMR and circular dichroic (CD) spectra of tuftsin and its analogues are discussed in connection with the hypothesis that the .beta.-turn is the biologically active conformation of tuftsin. The changes in CD spectra evoked by an increase in pH are interpreted as a demonstration of the increasing amount of .beta.-turn conformers in solution. Configurational changes in successive residues of tuftsin showed that residues 2 and 3 of the peptide chain are important for the tuftsin conformation.