Issue 24, 2017

Balancing the intermolecular forces in peptide amphiphiles for controlling self-assembly transitions

Abstract

While the influence of alkyl chain length and headgroup size on self-assembly behaviour has been well-established for simple surfactants, the rational control over the pH- and concentration-dependent self-assembly behaviour in stimuli responsive peptides remains an elusive goal. Here, we show that different amphiphilic peptides can have similar self-assembly phase diagrams, providing the relative strengths of the attractive and repulsive forces are balanced. Using palmitoyl-YYAAEEEEK(DO3A:Gd)-NH2 and palmitoyl-YAAEEEEK(DO3A:Gd)-NH2 as controls, we show that reducing hydrophobic attractive forces through fewer methylene groups in the alkyl chain will lead to a similar self-assembly phase diagram as increasing the electrostatic repulsive forces via the addition of a glutamic acid residue. These changes allow creation of self-assembled MRI vehicles with slightly different micelle and nanofiber diameters but with minimal changes in the spin–lattice T1 relaxivity. These findings reveal a powerful strategy to design self-assembled vehicles with different sizes but with similar self-assembly profiles.

Graphical abstract: Balancing the intermolecular forces in peptide amphiphiles for controlling self-assembly transitions

Supplementary files

Article information

Article type
Paper
Submitted
07 apr 2017
Accepted
29 may 2017
First published
30 may 2017

Org. Biomol. Chem., 2017,15, 5220-5226

Balancing the intermolecular forces in peptide amphiphiles for controlling self-assembly transitions

C. J. Buettner, A. J. Wallace, S. Ok, A. A. Manos, M. J. Nicholl, A. Ghosh, M. F. Tweedle and J. E. Goldberger, Org. Biomol. Chem., 2017, 15, 5220 DOI: 10.1039/C7OB00875A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements