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Title: | Metal-Ion-Induced Evolution of Phenylalanine Self-Assembly: Structural Polymorphism of Novel Metastable Intermediates |
Authors: | Bagchi, Debanjan Maity, Avijit De, Soumya Kanti Chakraborty, Anjan |
Keywords: | Amino acids;Assembly;Drug delivery;Hydrophobicity;Metals;Polymorphism;Self assembly;Tissue engineering;Amino-acids;Aqueous media;Aromatic amino acid;Divalents;Fibrillar structures;Intermediate state;Metals ions;Metastable intermediate;Self assembly process;Structural polymorphisms;Metal ions |
Issue Date: | 2022 |
Publisher: | American Chemical Society |
Citation: | Bagchi, D., Maity, A., De, S. K., & Chakraborty, A. (2022). Metal-ion-induced evolution of phenylalanine self-assembly: Structural polymorphism of novel metastable intermediates. Journal of Physical Chemistry Letters, , 10409-10417. doi:10.1021/acs.jpclett.2c02882 |
Abstract: | The self-assembly of aromatic amino acids has been widely studied due to their ability to form well-defined amyloid-like fibrillar structures. Herein, for the first time, we report the existence of different metastable intermediate states of diverse morphologies, for example, droplets, spheres, vesicles, flowers, and toroids, that are sequentially formed in aqueous medium during the self-assembly process of phenylalanine in the presence of different divalent (Zn2+, Cd2+, and Hg2+) and trivalent (Al3+, Ga3+, and In3+) metal ions having low pKa values. Due to metal ion-amino acid coordination and strong hydrophobic interaction induced by these metal ions, spherical aggregates are obtained at the initial stage of the structural evolution and further transformed into other intermediate states. Our work may facilitate understanding of the role of metal ions in the amino acid self-assembly process and broaden future applications of the obtained nanostructures in drug delivery, tissue engineering, bioimaging, biocatalysis, and other fields. © 2022 American Chemical Society. |
URI: | https://doi.org/10.1021/acs.jpclett.2c02882 https://dspace.iiti.ac.in/handle/123456789/11100 |
ISSN: | 1948-7185 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Chemistry |
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