UV resonance Raman investigation of the conformations and lowest energy allowed electronic excited states of tri- and tetraalanine: Charge transfer transitions

摘要

UV resonance Raman excitation profiles and Raman depolarization ratios were measured for trialanine and tetraalanine between 198 and 210 nm. Excitation within the π → π* electronic transitions of the peptide bond results in UVRR spectra dominated by amide peptide bond vibrations. In addition to the resonance enhancement of the normal amide vibrations, we find enhancement of the symmetric terminal COO - vibration. The Ala 3 UVRR AmIII 3 band frequencies indicate that poly-proline II and 2.5 1 helix conformations and type II turns are present in solution. We also find that the conformation of the interior peptide bond of Ala 4 is predominantly poly-proline-II-like. The Raman excitation profiles of both Ala 3 and Ala 4 reveal a charge transfer electronic transition at 202 nm, where electron transfer occurs from the terminal nonbonding carboxylate orbital to the adjacent peptide bond π* orbital. Raman depolarization ratio measurements support this assignment. An additional electronic transition is found in Ala 4 at 206 nm. © 2010 American Chemical Society.