ABSTRACT
Based on ß-turn-like BDNF loops 2 and 4, involved in receptor interaction, cyclic peptide replicas were designed, synthesized and tested. In addition to the native turn residues, the cyclic peptides include a linker unit between the N- and C-termini, selected by molecular modeling among various non-proteinogenic cyclic amino acids. NMR conformational studies showed that most of the cyclic peptides were able to adopt turn-like structures. Several of the analogues displayed significant inhibition of the BDNF-induced TrkB receptor phosphorylation, and hence could be useful templates for developing improved antagonists for this receptor.
Subject(s)
Amino Acids, Cyclic/chemistry , Brain-Derived Neurotrophic Factor/chemistry , Receptor, trkB/chemistry , Brain-Derived Neurotrophic Factor/metabolism , Chromatography, High Pressure Liquid/methods , Drug Design , Humans , Magnetic Resonance Spectroscopy/methods , Models, Chemical , Molecular Conformation , Peptides/chemistry , Peptides, Cyclic/chemistry , Phosphorylation , Protein Conformation , Protein Structure, Secondary , Protein Structure, Tertiary , TemperatureABSTRACT
Conveniently substituted 2-alkyl-2-carboxyazetidine amino acids have been incorporated into NGF and NT3 tetrapeptide sequences to investigate their utility as reverse turn inducers (γ- vs. ß-turns). Despite the presence of an Asp residue at i position, highly preferred in ß-turns, molecular modeling and NMR studies indicated that the azetidine-containing peptides mainly stabilized γ-turn conformations.
Subject(s)
Azetidines/chemistry , Nerve Growth Factors/chemistry , Peptide Fragments/chemistry , Azetidines/chemical synthesis , Models, Molecular , Peptide Fragments/chemical synthesisABSTRACT
Reverse turns, a common motif in proteins and peptides, have attracted attention due to their relevance in a wide variety of biological processes. In an attempt to artificially imitate and stabilize these turns in short peptides, we have developed versatile synthetic methodologies for the preparation of 2-alkyl-2-carboxyazetidines and incorporated them into the i + 1 position of model tetrapeptides, where they have shown a tendency to induce gamma-turns. However, to ascertain the general utility of these restricted amino acids as gamma-type reverse turn inducers, it was then required to study the conformational preferences when located at other positions. To this end, model tetrapeptides R-CO-Ala-Xaa-NHMe, containing differently substituted azetidine moieties (Xaa = Aze, 2-MeAze, 2-BnAze) at the i + 2 position, were synthesized and subjected to a thorough conformational analysis. The theoretical and experimental results obtained, including the X-ray diffraction structure of a dipeptide derivative containing this skeleton, provide evidence that the 2-alkyl-2-carboxyazetidine scaffold is able to efficiently induce gamma-turns when incorporated into these short peptides, irrespective of their localization in the peptide chain.
Subject(s)
Azetidines/chemistry , Models, Molecular , Molecular Conformation , Spectrometry, Mass, Electrospray Ionization , Spectroscopy, Fourier Transform Infrared , X-Ray DiffractionABSTRACT
A series of constrained pentapeptide analogues of the fragment Abeta(31-35) has been prepared using solid phase synthesis protocols. The results of conformational studies and surface plasmon resonance (SPR) experiments seem to indicate that the affinity of these constrained analogues for immobilized Abeta(25-35) peptide could be related to their ability to adopt a Leu34N-Ile31O beta-turn-like folded conformation.
Subject(s)
Amyloid beta-Peptides/chemistry , Amyloid beta-Peptides/chemical synthesis , Amyloid beta-Peptides/pharmacology , Animals , Blotting, Western , Cell Survival , Cells, Cultured , Hippocampus/cytology , Hippocampus/metabolism , Immobilization , Molecular Structure , Neurons/cytology , Neurons/metabolism , Protein Structure, Secondary , Rats , Rats, Wistar , Surface Plasmon ResonanceABSTRACT
The influence of 2-alkyl-2-carboxyazetidines (Aze) on the 3D structure of model tetrapeptides R2CO-2-R1Aze-l-Ala-NHMe has been analyzed by molecular modeling, 1H NMR, and FT-IR studies. The conformational constraints introduced by the four-membered ring resulted in an effective way to stabilize gamma-turn-like conformations in these short peptides. The conformational preferences of these Aze-containing peptides have been compared to those of the corresponding peptide analogues containing Pro or alpha-MePro in the place of 2-alkyl-Aze residue. In the model studied, both Pro and Aze derivatives are able to induce reverse turns, but the nature of the turn is different as a function of the ring size. While the five-membered ring of Pro tends to induce beta-turns, as previously suggested by different authors, the four-membered ring of Aze residues forces the peptide to preferentially adopt gamma-turn conformations. In both cases, the presence of an alkyl group at the alpha-position of Pro or the azetidine-2-carboxylate ring enhances significantly the turn-inducing ability. These results might open the opportunity of using 2-alkyl-Aze residues as versatile tools in defining the role of gamma-turn structures within the bioactive conformation of selected peptides, and represent an alternative to Pro derivatives as turn inducers.
