DNA G-Wire Formation Using an Artificial Peptide is Controlled by Protease Activity

The development of a switching system for guanine nanowire (G-wire) formation by external signals is important for nanobiotechnological applications. Here, we demonstrate a DNA nanostructural switch (G-wire particles) using a designed peptide and a protease. The peptide consists of a PNA sequence f...

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2017-11, Vol.22 (11), p.1991
Hauptverfasser: Usui, Kenji, Okada, Arisa, Sakashita, Shungo, Shimooka, Masayuki, Tsuruoka, Takaaki, Nakano, Shu-Ichi, Miyoshi, Daisuke, Mashima, Tsukasa, Katahira, Masato, Hamada, Yoshio
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Sprache:eng
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Zusammenfassung:The development of a switching system for guanine nanowire (G-wire) formation by external signals is important for nanobiotechnological applications. Here, we demonstrate a DNA nanostructural switch (G-wire particles) using a designed peptide and a protease. The peptide consists of a PNA sequence for inducing DNA to form DNA-PNA hybrid G-quadruplex structures, and a protease substrate sequence acting as a switching module that is dependent on the activity of a particular protease. Micro-scale analyses via TEM and AFM showed that G-rich DNA alone forms G-wires in the presence of Ca , and that the peptide disrupted this formation, resulting in the formation of particles. The addition of the protease and digestion of the peptide regenerated the G-wires. Macro-scale analyses by DLS, zeta potential, CD, and gel filtration were in agreement with the microscopic observations. These results imply that the secondary structure change (DNA G-quadruplex DNA/PNA hybrid structure) induces a change in the well-formed nanostructure (G-wire particles). Our findings demonstrate a control system for forming DNA G-wire structures dependent on protease activity using designed peptides. Such systems hold promise for regulating the formation of nanowire for various applications, including electronic circuits for use in nanobiotechnologies.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules22111991