Wydział Chemii

Cristina Puzzarini

Małgorzata Biczysko

Vincenzo Barone

Laura Largo

Isabel Peña

Carlos Cabezas

José Luis Alonso

2014

Journal of Physical Chemistry Letters

5

534-540

10.1021/jz402744a

Naukowa

Angielski

Artykuł

Accurate structures of aminoacids in the gas phase have been obtained by joint microwave and quantum-chemical investigations. However, the structure and conformational behavior of α-aminoacids once incorporated into peptide chains are completely different and have not yet been characterized with the same accuracy. To fill this gap, we present here an accurate characterization of the simplest dipeptide analogue (N-acetyl-glycinamide) involving peptidic bonds. State-of-the-art quantum-chemical computations are complemented by a comprehensive study of the rotational spectrum using a combination of Fourier transform microwave spectroscopy with laser ablation. The coexistence of the C₇ and C₅ conformers has been proved and energetically as well as spectroscopically characterized. This joint theoretical-experimental investigation demonstrated the feasibility of obtaining accurate structures for flexible small biomolecules, thus paving the route to the elucidation of the inherent behavior of peptides.

glycine dipeptide analogue, quantum-chemical calculations, composite scheme, rotational spectrum, laser ablation

http://dx.doi.org/10.1021/jz402744a

https://www.acs.org/content/acs/en.html