2012
DOI: 10.1039/c2cc31872e
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Control of peptide assembly through directional interactions

Abstract: We demonstrate the self-assembly of tripeptide amphiphiles into spherical hollow capsules from linear nanoribbons via control of the molecular packing. We achieved a transition of arrangement from anisotropic to isotropic by an elaborate design of the molecular architecture.

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Cited by 34 publications
(30 citation statements)
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“…Moreover, some multivalent nanofibrils have shown the propensity to selectively kill bacteria but spare tissue cells . Despite the significant application potential, the construction of those nanofibers is limited to the spontaneous assembly of β‐sheet peptides …”
Section: Figurementioning
confidence: 99%
“…Moreover, some multivalent nanofibrils have shown the propensity to selectively kill bacteria but spare tissue cells . Despite the significant application potential, the construction of those nanofibers is limited to the spontaneous assembly of β‐sheet peptides …”
Section: Figurementioning
confidence: 99%
“…Variation of the functional groups at the N-termini results in different morphological outcomes. 41 7…”
Section: Figurementioning
confidence: 99%
“…[11] Moreover,s ome multivalent nanofibrils have shown the propensity to selectively kill bacteria but spare tissue cells. [13,14] We are interested in developing multivalent peptide nanofibers with synthetic versatility beyond the reported strategy.Ithas been established that ionic self-assembly (ISA) between cationic peptides and polyanions is aconvenient and effective way to produce fibril-like nanostructures. [13,14] We are interested in developing multivalent peptide nanofibers with synthetic versatility beyond the reported strategy.Ithas been established that ionic self-assembly (ISA) between cationic peptides and polyanions is aconvenient and effective way to produce fibril-like nanostructures.…”
Section: Multivalent Electrostatic Interactions Between Cationicmentioning
confidence: 99%
“…However,abisignate positive band at 197 nm together with an egative Cotton effect at 214 nm were observed in CD spectra ( Figure 2) upon the addition of H 4 SiW 12 O 40 (HSiW,F igure 1b)toan aqueous solution of L1, thus demonstrating the commencement of ac onformation transition from ar andom-coil to a b-sheet state. [13] The intensity of the negative signal at 214 nm increased gradually until am aximal b-sheet content was reached with am olar ratio of L1 to HSiW (M L1/HSiW )near 2:1. Afurther increase in the stoichiometry of HSiW led to precipitation of the material and thereby the disappearance of the CD signal.…”
mentioning
confidence: 98%
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