A linear amphoteric poly(amidoamino acid), L-ARGO7, is prepared by Michael-type polyaddition of L-arginine with N,N'-methylenebisacrylamide. Chain-extension of acrylamide end-capped L-ARGO7 oligomers with piperazine leads to high-molecular-weight copolymers in which L-arginine maintains its absolute configuration. Acid/base properties of L-ARGO7 polymers show isolectric points of ≈ 10 and positive net average charges per repeating unit at pH = 7.4 from 0.25 to 0.40. These arginine-rich synthetic polymers possibly share some of the unique biological properties of polyarginine cell-permeating peptides. In vitro tests with mouse embryo fibroblasts balb/3T3 clone A31 show that L-ARGO7 polymers are endowed with effective cell internalization ability combined with minimal cytotoxicity.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/mabi.201300387 | DOI Listing |
Polymers (Basel)
April 2020
Faculty of Engineering and Science, University of Greenwich, Medway Campus, Chatham Maritime, Kent ME4 4TB, UK.
- and -arginine-based polyamidoamino acids, called - and -ARGO7, retain the chirality and acid/base properties of the parent -amino acids and show pH-dependent self-structuring in water. The ability of the ARGO7 chiral isomers to selectively interact with chiral biomolecules and/or surfaces was studied by choosing sodium deoxycholate (NaDC) as a model chiral biomolecule for its ability to self-assembly into globular micelles, showing enantio-selectivity. To this purpose, mixtures of NaDC with -, - or -ARGO7, respectively, in water were analysed by circular dichroism (CD) spectroscopy and small-angle neutron scattering (SANS) at different levels of acidity expressed in terms of pD and concentrations.
View Article and Find Full Text PDFPolymers (Basel)
April 2020
Dipartimento di Chimica, Università degli Studi di Milano, via C. Golgi 19, 20133 Milano, Italy.
This paper reports on synthesis, acid-base properties, and self-structuring in water of a chiral polyamidoamino acid, M--Gln, obtained from the polyaddition of -methylenebisacrylamide with -glutamine, with the potential of establishing hydrogen bonds through its -amide pendants. The M--Gln showed pH-responsive circular dichroism spectra, revealing ordered conformations. Structuring was nearly insensitive to ionic strength but sensitive to denaturing agents.
View Article and Find Full Text PDFPolymers (Basel)
August 2019
Dipartimento di Chimica, Università degli Studi di Milano, via C. Golgi 19, 20133 Milano, Italy.
Polyamidoamino acids (PAACs) are synthetic polymers prepared by the polyaddition of bisacrylamides with natural α-amino acids, which in the process maintain both their chirality and their amphoteric nature. This polymerization process is slow, but has the merits of taking place in water and of neither involving protection/de-protection steps nor releasing by-products. However, it leads to polydisperse polymers and, using α-amino acids mixtures, random copolymers.
View Article and Find Full Text PDFPolymers (Basel)
November 2018
Dipartimento di Chimica, Università degli Studi di Milano, via C. Golgi 19, 20133 Milano, Italy.
This paper reports on synthesis, acid-base properties and self-structuring in water of chiral polyamidoamino acids (PAACs) obtained by polyaddition of ,'-methylenebisacrylamide with -alanine, -valine and -leucine (M--Ala, M--Val, M--Leu) with potential for selective interactions with biomolecules. The polymers maintained the acid-base properties of amino acids. In water, the circular dichroism spectra of PAACs revealed pH-dependent structuring in the range 3⁻11 and in the wavelength interval 200⁻280 nm.
View Article and Find Full Text PDFPolymers (Basel)
March 2019
Dipartimento di Chimica, Università degli Studi di Milano, via C. Golgi 19, 20133 Milano, Italy.
Chiral polyamidoamino acids were obtained by polyaddition of -methylenebisacrylamide with -, ,- and -tryptophan (M--Trp, M--Trp and M--Trp). -tryptophan/glycine copolymers, M-G--Trp₅, M-G--Trp, M-G--Trp and M-G--Trp were prepared from -tryptophan/glycine mixtures. These polymers were amphoteric, with acid-base properties similar to those of the parent amino acids.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!