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As part of an in-vitro/in-silico study carried out at Santiago de Compostela University to deeply analyze the preferred rearrangement adopted by α,γ-CPs, we explored all the possible combinations that could take place starting from two different monomers and their corresponding enantiomers.[1] This approach uses the selective N-methylation of the amide groups whose protons are not involved in hydrogen bonding interactions.  When the tracker images of two monomers are placed close to each other, the structure of the dimer formed by that combination of cyclic peptides is shown.  The cyclic peptides (CPs) are composed by γ-amino acids (cis-α,γ-aminocycloalkanecarboxylic acids, γ-Acas) alternated with α-amino acids (α,γ-CPs).  cette application allows visualizing different supramolecular dimeric complexes of cyclic peptides in Augmented Reality (AR).  These peptides containing γ-Acas can be designed from the original D,L-α-CPs just by replacing any α-amino acid for a γ-Aca of equivalent chirality.  Full geometry optimizations of the dimers and monomers were carried out with the B3LYP functional and the standard 6-31G(d) basis set.  Depending on the combination of monomers, a parallel or an antiparallel arrangement is possible.  This application was specifically developed by Santiago de Compostela University (Spain) and MD.USE Innovative Solutions S.L. ( ).  For instance, L-amino acids can be replaced by (1R,3S)-isomers while the (1S,3R)-Acas would substitute the D-enantiomers.  Pointing with the device to each tracker separately, an AR image of the corresponding monomer is viewed.  All of the DFT calculations reported in this study were performed with the Gaussian 16 package.  The N-methylated residues are indicated in the figures of the trackers.