A.S. Morozova a*, E.O. Kudryavtseva a,b**,
S.A. Ziganshina a,b***, M.A. Ziganshin b****, A.A. Bukharaev a*****
aZavoisky Physical-Technical Institute, FRC Kazan Scientific Center,
Russian Academy of Sciences, Kazan, 420029 Russia
bKazan Federal University, Kazan, 420008 Russia
E-mail: *morozova_anna_s@mail.ru, **justqu1@yandex.ru, ***sufia@knc.ru,
****Marat.Ziganshin@kpfu.ru, *****a_bukharaev@mail.ru
Received December 26, 2022; Accepted February 6, 2023
ORIGINAL ARTICLE
Full text PDF
DOI: 10.26907/2542-064X.2023.1.37-48
For citation: Morozova A.S., Kudryavtseva E.O., Ziganshina S.A., Ziganshin M.A., Bukharaev A.A. Self-assembly of the dipeptide L-alanyl-L-phenylalanine under the action of methanol vapor with the formation of micro- and nanostructures. Uchenye Zapiski Kazanskogo Universiteta. Seriya Estestvennye Nauki, 2023, vol. 165, no. 1, pp. 37–48. doi: 10.26907/2542-064X.2023.1.37-48. (In Russian)
Abstract
The mechanism of self-assembly by short-chain peptides (oligopeptides) – the process by which their molecules spontaneously form an ordered structure – has received much attention recently. Self-assembling phenylalanine oligopeptides have been of particular interest due to their potential as an effective aid in the design of new functional materials. This paper considers the results of an SPM study on the ability of L-alanyl-L-phenylalanine to self-assemble into a thin film under the action of methanol vapor. The micro- and nanostructures that develop on the surface of amorphous films of this dipeptide were characterized. A method for monitoring the state of the surface of dipeptide films using atomic force spectroscopy was proposed. The results obtained contribute to the development of approaches for the controlled self-assembly of oligopeptides used to produce new biocompatible materials and environmentally friendly micro- and nanodevices that would help solve various problems in the medical, environmental, and energy fields.
Keywords: dipeptides, self-assembly, thin films, microstructures, nanostructures, atomic force microscopy
Acknowledgements. This study was performed under the state assignment to the FRC Kazan Scientific Center, Russian Academy of Sciences (A.S. Morozova, E.O. Kudryavtseva, A.A. Bukharaev) and supported by the Kazan Federal University Strategic Academic Leadership Program (PRIORITY-2030) (S.A. Ziganshina, M.A. Ziganshin).
Figure Captions
Fig. 1. Structural formula of the dipeptide AlaPhe.
Fig. 2. AFM images of the AlaPhe films obtained from the solution in MeOH (1 mg/mL) (a) and HFIP (1 mg/mL) (b) by self-drying.
Fig. 3. AFM images of the AlaPhe films obtained from the solution in MeOH (1 mg/mL) (a) and HFIP (1 mg/mL) (b) by forced drying.
Fig. 4. AFM images of the AlaPhe films obtained from the solution in MeOH (1 mg/mL) (a) and HFIP (1 mg/mL) (b) by forced drying after saturation with MeOH vapor for 10 min.
Fig. 5. AFM images of the AlaPhe films obtained from the solution in methanol (1 mg/mL) (a) and HFIP (1 mg/mL) (b) by forced drying after saturation with methanol vapor for 30 min.
Fig. 6. AFM images of the AlaPhe films obtained from the solution in MeOH (1 mg/mL) (a) and HFIP (1 mg/mL) (b) by forced drying after saturation with MeOH vapor for 60 min.
Fig. 7. Curves obtained in the atomic force spectroscopy mode for an amorphous AlaPhe film.
References
- Ekiz M.S., Cinar G., Khalily M.A., Guler M.O. Self-assembled peptide nanostructures for functional materials. Nanotechnology, 2016, vol. 27, no. 40, art. 402002. doi: 10.1088/0957-4484/27/40/402002.
- D’Orlyé F., Trapiella-Alfonso L., Lescot C., Pinvidic M., Doan B.T., Varenne A. Synthesis, characterization and evaluation of peptide nanostructures for biomedical applications. Molecules, 2021, vol. 26, no. 15, art. 4587. doi: 10.3390/molecules26154587.
- Liu N., Zhu L., Li Z., Liu W., Sun M., Zhou Z. In situ self-assembled peptide nanofibers for cancer theranostics. Biomater. Sci., 2021, vol. 9, pp. 5457–5466. doi: 10.1039/d1bm00782c.
- Guo C., Luo Y., Zhou R., Wei G. Triphenylalanine peptides self-assemble into nanospheres and nanorods that are different from the nanovesicles and nanotubes formed by diphenylalanine peptides. Nanoscale, 2014, vol. 6, no. 5, pp. 2800–2811. doi: 10.1039/C3NR02505E.
- Naskar J., Banerjee A. Concentration dependent transformation of oligopeptide based nanovesicles to nanotubes and an application of nanovesicles. Asian J., 2009, vol. 4, no. 12, pp. 1817–1823. doi: 10.1002/asia.200900274.
- Adler-Abramovich L., Gazit E. The physical properties of supramolecular peptide assemblies: From building block association to technological applications. Chem. Soc. Rev., 2014, vol. 43, no. 20, pp. 6881–6893. doi: 10.1039/C4CS00164H.
- Yan X., Li J., Möhwald H. Self-assembly of hexagonal peptide microtubes and their optical waveguiding. Adv. Mater., 2011, vol. 23, no. 25, pp. 2796–2801. doi: 10.1002/adma.201100353.
- Adler-Abramovich L., Kol N., Yanai I., Barlam D., Shneck R.Z., Gazit E., Rousso I. Self-assembled organic nanostructures with metallic-like stiffness. Angew. Chem., 2010, vol. 49, no. 51, pp. 9939–9942. doi: 10.1002/anie.201002037.
- Ryan K., Beirne J.G., Redmond G., Kilpatrick J.I., Guyonnet J., Buchete N.V., Kholkin A.L., Rodriguez B.J. Nanoscale piezoelectric properties of self-assembled Fmoc-FF peptide fibrous networks. ACS Appl. Mater. Interfaces, 2015, vol. 7, no. 23, pp. 12702–12707. doi: 10.1021/acsami.5b01251.
- Fan T., Yu X., Shen B., Sun L. Peptide self-assembled nanostructures for drug delivery applications. J. Nanomater., 2017, vol. 2017, art. 4562474. doi: 10.1155/2017/4562474.
- Habibi N., Kamaly N., Memic A., Shafiee H. Self-assembled peptide-based nanostructures: Smart nanomaterials toward targeted drug delivery. Nano Today, 2016, vol. 11, no. 1, pp. 41–60. doi: 10.1016/j.nantod.2016.02.004.
- Kim S., Kim J.H., Lee J.S., Park C.B. Beta-sheet-forming, self-assembled peptide nanomaterials towards optical, energy, and healthcare applications. Small, 2015, vol. 11, no. 30, pp. 3623–3640. doi: 10.1002/smll.201500169.
- Fan Z., Sun L., Huang Y., Wang Y., Zhang M. Bioinspired fluorescent dipeptide nanoparticles for targeted cancer cell imaging and real-time monitoring of drug release. Nat. Nanotechnol., 2016, vol. 11, no. 4, pp. 388–394. doi: 10.1038/nnano.2015.312.
- Tao K., Makam P., Aizen R., Gazit E. Self-assembling peptide semiconductors. Science, 2017, vol. 358, no. 6365, art. eaam9756, pp. 1–7. doi: 10.1126/science.aam9756.
- Yuran S., Razvag Y., Reches M. Coassembly of aromatic dipeptides into biomolecular necklaces. ACS Nano, 2012, vol. 6, no. 11, pp. 9559–9566. doi: 10.1021/nn302983e.
- Ryu J., Park Ch.B. High-temperature self-assembly of peptides into vertically well-aligned nanowires by aniline vapor. Adv. Mater., 2008, vol. 20, no. 19, pp. 3754–3758. doi: 10.1002/adma.200800364.
- Morozova A.S., Ziganshina S.A., Bukharaev A.A., Ziganshin M.A., Gerasimov A.V. Features of the self-organization of films based on triglycine under the influence of vapors of organic compounds. J. Surf. Invest., 2020, vol. 3, pp. 73–81. doi: 10.1134/S102745102003009X.
- Ziganshin M.A., Morozova A.S, Ziganshina S.A., Vorobev V.V., Suwińska K., Bukharaev A.A., Gorbatchuk V.V. Additive and antagonistic effects of substrate and vapors on self-assembly of glycyl-glycine in thin films. Mol. Cryst. Liq. Cryst., 2019, vol. 690, no. 1, pp. 67–83. doi: 10.1080/15421406.2019.1683311.
- Arutyunov P.A., Tolstikhina A.L. Atomic force microscopy in designing micro- and nanoelectronic devices. Mikroelektronika, 1999, vol. 28, no. 6, pp. 405–414. (In Russian)
- Morozova A.S., Ziganshina S.A., Ziganshin M.A., Bukharaev A.A. Self-organization of di- and triglycine oligopeptides in thin films on the hydrophilic and hydrophobic silicon surface under exposure to organic compounds vapors. Russ. J. Gen. Chem., 2022, vol. 92, no. 7, pp. 1271–1279. doi: 10.1134/S1070363222070155.
The content is available under the license Creative Commons Attribution 4.0 License.