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Self-Assembly of Diphenylalanine-Peptide Nucleic Acid Conjugates.

ABSTRACT: The synthesis and self-assembled nanostructures of a series of nucleopeptides (NPs) derived from the dipeptide Phe-Phe and the peptide nucleic acid unit which are covalently attached through an amide or a triazole linker are described. Depending on the variables such as protecting groups, linkers, and nucleobases, spherical nanoparticles were observed through scanning electron microscopy and high-resolution transmission electron microscopy images, and the porous nature of representative NPs was corroborated by carboxyfluorescein entrapment. Hydrophobic substituents on different sites of NPs and solvents employed for peptide self-assembly played a crucial role for corresponding morphologies. The stability of nanoparticles was also probed under external stimuli such as pH, temperature, and enzymatic hydrolysis using proteolytic enzymes. The semiconducting nature of the NP-modified carbon electrodes suggested their potential use as a new capacitor material.

SUBMITTER: Datta D

PROVIDER: S-EPMC6649282 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

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Self-Assembly of Diphenylalanine-Peptide Nucleic Acid Conjugates.

Datta Dhrubajyoti D Tiwari Omshanker O Gupta Manoj Kumar MK

ACS omega 20190620 6

The synthesis and self-assembled nanostructures of a series of nucleopeptides (NPs) derived from the dipeptide Phe-Phe and the peptide nucleic acid unit which are covalently attached through an amide or a triazole linker are described. Depending on the variables such as protecting groups, linkers, and nucleobases, spherical nanoparticles were observed through scanning electron microscopy and high-resolution transmission electron microscopy images, and the porous nature of representative NPs was ...[more]

PMID: 31460170

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