The construction of well-defined nanostructures from the self-assembly of small organic molecules has gained increasing attention in the last decade [1]. The use of peptides, in particular, gives access to different ordered and, in some case, intricate morphologies [2]. For this high structural variability, peptide-based supramolecular assemblies are of valuable interest in biological systems as transmembrane pores models, ion channels mimics, and as drug delivery vehicles [3]. On the other hand, one drawback of using peptides for biomedical applications is their high susceptibility toward proteases and their short half-lives. The use of unnatural amino acids, such as alpha-alpha-disubstituted, beta-, and D-amino acids, is a profitable strategy to overcome these issues [3c, 4].

Self-assembly of dipeptide nanotubes constituted by (S,S) beta-diarylaminoacid and (L)-alanine, as putative drug delivery system / S. Pellegrino, A. Bonetti, F. Meneghetti, M.L. Gelmi, M. Reiches - In: Nanomedicine: pharmacokinetic challenges, targeting and clinical outcomes[s.l] : CRS Italy Chapter, 2014 Nov 07. (( convegno CRS Workshop tenutosi a Firenze nel 2014.

Self-assembly of dipeptide nanotubes constituted by (S,S) beta-diarylaminoacid and (L)-alanine, as putative drug delivery system

S. Pellegrino
Primo
;
A. Bonetti
Secondo
;
F. Meneghetti;M.L. Gelmi
Penultimo
;
2014

Abstract

The construction of well-defined nanostructures from the self-assembly of small organic molecules has gained increasing attention in the last decade [1]. The use of peptides, in particular, gives access to different ordered and, in some case, intricate morphologies [2]. For this high structural variability, peptide-based supramolecular assemblies are of valuable interest in biological systems as transmembrane pores models, ion channels mimics, and as drug delivery vehicles [3]. On the other hand, one drawback of using peptides for biomedical applications is their high susceptibility toward proteases and their short half-lives. The use of unnatural amino acids, such as alpha-alpha-disubstituted, beta-, and D-amino acids, is a profitable strategy to overcome these issues [3c, 4].
Settore CHIM/06 - Chimica Organica
   Piano Sviluppo Unimi - LINEA B - DOTAZIONE ANNUALE PER ATTIVITA' ISTITUZIONALI
7-nov-2014
Book Part (author)
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/244143
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact