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High-Resolution Terahertz Spectroscopy of Crystalline Trialanine: Extreme Sensitivity to β-Sheet Structure and Cocrystallized Water

2006; American Chemical Society; Volume: 128; Issue: 17 Linguagem: Inglês

10.1021/ja058176u

1943-2984

K. Siegrist, Christine Bucher, Idan Mandelbaum, Angela R. Hight Walker, Radhakrishnan Balu, Susan Gregurick, David F. Plusquellic,

Advanced Chemical Physics Studies

High-resolution terahertz absorption spectra (0.06−3 THz) have been obtained at 4.2 K for three crystalline forms of trialanine [H2+-(Ala)3-O-]. The crystal structures differ in their β-sheet forms (parallel vs antiparallel) and in their water composition (hydrated vs dehydrated antiparallel β-sheet). The spectra are nearly vibrationally resolved, with little absorption below 1 THz. In sharp contrast to observations made in the mid-IR region, the spectral patterns of all three forms are qualitatively different, illustrating the extreme sensitivity to changes in the intermolecular hydrogen-bonding networks that stabilize peptide crystals. Predictions obtained from a classical force field model (CHARMM) and density functional theory (DFT/PW91) for periodic solids are compared with the X-ray structural data and the terahertz absorption spectra. In general, the results for the parallel β-sheet are in better agreement with experiment than those for the antiparallel β-sheet. For all three structures, however, most hydrogen bond distances are underestimated at both levels of theory, and the predicted absorption features are significantly red-shifted for the two antiparallel β-sheet structures. Moreover, the nuclear motions predicted at the two levels of theory are qualitatively different. These results indicate that the PW91 functional is not sufficient to treat the weak intersheet hydrogen bonding present in the different β-sheet forms and strongly suggest the need for improved force field models that include three-atom hydrogen-bonding terms for periodic solids.