Hierarchical self-assembly of di-, tri- and tetraphenylalanine peptides capped with two fluorenyl functionalities: from polymorphs to dendrites

Author

Mayans, Enric

Ballano, Gema

Casanovas Salas, Jordi

Valle, Luis J. del

Pérez-Madrigal, Maria M.

Estrany, Francesc

Jiménez, Ana I.

Puiggalí, Jordi

Cativiela, Carlos

Alemán, Carlos

Publication date

2018-11-07T10:26:03Z

2018-11-07T10:26:03Z

2016



Abstract

Homopeptides with 2, 3 and 4 phenylalanine (Phe) residues and capped with fluorenylmethoxycarbonyl and fluorenylmethyl esters at the N-terminus and C-terminus, respectively, have been synthesized to examine their self-assembly capabilities. Depending on the conditions, the di- and triphenylalanine derivatives self-organize into a wide variety of stable polymorphic structures, which have been characterized: stacked braids, doughnut-like shapes, bundled arrays of nanotubes, corkscrew-like shapes and spherulitic microstructures. These highly aromatic Phe-based peptides also form incipient branched dendritic microstructures, even though they are highly unstable, making their manipulation very difficult. Conversely, the tetraphenylalanine derivative spontaneously self-assembles into stable dendritic microarchitectures made of branches growing from nucleated primary frameworks. The fractal dimension of these microstructures is ∼1.70, which provides evidence for self-similarity and two-dimensional diffusion controlled growth. DFT calculations at the M06L/6-31G(d) level have been carried out on model β-sheets since this is the most elementary building block of Phe-based peptide polymorphs. The results indicate that the antiparallel β-sheet is more stable than the parallel one, with the difference between them growing with the number of Phe residues. Thus, the cooperative effects associated with the antiparallel disposition become more favorable when the number of Phe residues increases from 2 to 4, while those of the parallel disposition remained practically constant.


The authors thank the support from MINECO and FEDER (MAT2012-34498, MAT2012-36205 and CTQ2013-40855-R), Generalitat de Catalunya (XRQTC) and CESCA and Gobierno de Aragón – Fondo Social Europeo (research group E40). Support for the research of C. A. was received through the prize ‘‘ICREA Academia’’ for excellence in research funded by the Generalitat de Catalunya.

Document Type

Article
Accepted version

Language

English

Publisher

Royal Society of Chemistry

Related items

info:eu-repo/grantAgreement/MINECO//MAT2012-34498/ES/

info:eu-repo/grantAgreement/MINECO//MAT2012-36205/ES/

info:eu-repo/grantAgreement/MINECO//CTQ2013-40855-R/ES/AMINOACIDOS NO PROTEICOS Y DERIVADOS PARA APLICACIONES EN AGROQUIMICA Y BIOMEDICINA/

Versió postprint del document publicat a https://doi.org/10.1039/C6SM00337K

Soft Matter, 2016, vol. 12, p. 5475-5488

Rights

(c) Royal Society of Chemistry, 2016

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