2013
DOI: 10.1016/j.colsurfb.2012.07.038
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Use of the self-assembly of tyrosine-containing bolaamphiphile molecules as a reactive template for metal deposition

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Cited by 20 publications
(21 citation statements)
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“…The shape of TyrBA was observed through electron microscopy in the presence of both the photosensitizer ([Ru(bpy) 3 Cl 2 ]) and the electron acceptor ([Co(NH 3 ) 5 Cl]Cl 2 ). The size of TyrBA was (85±5) nm in diameter with an indistinct boundary (Figure b), whereas intact TyrBA had a spherical structure with a smooth, well‐defined boundary (Figure c and Figure S2 in the Supporting Information) . The uneven boundary of TyrBA in the PSII mimetic system was presumably produced by aggregation of photosensitizer and/or electron acceptor molecules during sample preparation.…”
Section: Resultssupporting
confidence: 56%
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“…The shape of TyrBA was observed through electron microscopy in the presence of both the photosensitizer ([Ru(bpy) 3 Cl 2 ]) and the electron acceptor ([Co(NH 3 ) 5 Cl]Cl 2 ). The size of TyrBA was (85±5) nm in diameter with an indistinct boundary (Figure b), whereas intact TyrBA had a spherical structure with a smooth, well‐defined boundary (Figure c and Figure S2 in the Supporting Information) . The uneven boundary of TyrBA in the PSII mimetic system was presumably produced by aggregation of photosensitizer and/or electron acceptor molecules during sample preparation.…”
Section: Resultssupporting
confidence: 56%
“…Aside from the tyrosine–photosensitizer conjugates, a tyrosine‐rich solid matrix is a promising platform for the preparation of a PSII mimetic system. We recently reported that tyrosyl bolaamphiphile assembly (TyrBA) could yield a proteinaceous nanoscale solid matrix with the exposure of densely packed tyrosine phenol groups on the surface . TyrBA displayed biochemical activities of the tyrosine phenol groups and exhibited outstanding mechanical strength that originated from intermolecular interactions, such as hydrophobic interactions and hydrogen bonds.…”
Section: Introductionmentioning
confidence: 73%
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“…The nonuniformity of the bolaamphiphile self-assembly implied that the self-organization of the His-C7 was not strongly regulated by intermolecular forces, presumably because of the rather weak polarity of histidine. The histidine imidazole is less polar and its driving force of self-assembly is not strong compared to other peptidic bolaamphiphiles that form well-organized structures [14]. It is also noticeable that the presence of other transition metal ion (i.e., Cd 2+ and Ni 2+ ) did not alter the shape of self-assembly, although another transition metal ion of Cu 2+ is known to bind histidine imidazoles, thereby influencing the morphology of histidyl bolaamphiphile self-assembly [15].…”
Section: Characterization Of Transition Metal-associated Bolaamphiphimentioning
confidence: 99%
“…Detailed synthetic protocols of each peptidic bolaamphiphile are reported in the literature. 13,18 Briefly, the amino acid C-termini of histidine and tyrosine were modified to benzyl ester moieties and were then conjugated with azelaic acid through amide bonds. The crude products of the peptidic bolaamphiphiles were purified by repeating crystallization to produce powdered products.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%