Co-assembly of Peptide Amphiphiles and Lipids into
Supramolecular Nanostructures Driven by Anion-pi Interactions
Yu, ZL (Yu, Zhilin)[ 1,10 ] ; Erbas, A (Erbas, Aykut)[ 2 ] ; Tantakitti, F (Tantakitti, Faifan)[ 2 ] ; Palmer, LC (Palmer, Liam C.)[ 1,3 ] ; Jackman, JA (Jackman, Joshua A.)[ 4,5 ] ; de la Cruz, MO (de la Cruz, Monica Olvera)[ 1,2,6 ] ; Cho, NJ (Cho, Nam-Joon)[ 4,5,7 ] ; Stupp, SI (Stupp, Samuel I.)[ 1,2,3,8,9 ]
JOURNAL OF
THE AMERICAN CHEMICAL SOCIETY, 2017, 139(23); 7823-7830
DOI: 10.1021/jacs.7b02058
WOS:000403631200029
Abstract
Co-assembly
of binary systems driven by specific non-covalent interactions can greatly
expand the structural and functional space of supramolecular nanostructures. We
report here on the self-assembly of peptide amphiphiles and fatty acids driven
primarily by anion-pi interactions. The peptide sequences investigated were
functionalized with a perfluorinated phenylalanine residue to promote anion-pi
interactions with carboxylate headgroups in fatty acids. These interactions
were verified here by NMR. and circular dichroism experiments as well as
investigated using atomistic simulations. Positioning the aromatic units close
to the N-terminus of the peptide backbone near the hydrophobic core of
cylindrical nanofibers leads to strong anion-pi interactions between both
components. With a low content of dodecanoic acid in this position, the
cylindrical morphology is preserved. However, as the aromatic units are moved
along, the peptide backbone away from the hydrophobic core, the interactions
with dodecanoic acid transform the cylindrical supramolecular morphology into
ribbon-like structures. Increasing the ratio of dodecanoic acid to PA leads to
either the formation of large vesicles in the binary systems where the anion-pi
interactions are strong, or a heterogeneous mixture of assemblies when the
peptide amphiphiles associate weakly with dodecanoic acid. Our findings reveal
how co-assembly involving designed specific interactions can drastically change
supramolecular morphology and even cross from nano to micro scales.