Fluorescent azobenzene-confined coiled-coil mesofibers

Fluorescent protein biomaterials have important applications such as bioimaging in pharmacological studies. Self-assembly of proteins, especially into fibrils, is known to produce fluorescence in the blue band. Capable of self-assembly into nanofibers, we have shown we can modulate its aggregation i...

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Veröffentlicht in:Soft matter 2023-01, Vol.19 (3), p.497-51
Hauptverfasser: Punia, Kamia, Britton, Dustin, Hüll, Katharina, Yin, Liming, Wang, Yifei, Renfrew, P. Douglas, Gilchrist, M. Lane, Bonneau, Richard, Trauner, Dirk, Montclare, Jin K
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Sprache:eng
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Zusammenfassung:Fluorescent protein biomaterials have important applications such as bioimaging in pharmacological studies. Self-assembly of proteins, especially into fibrils, is known to produce fluorescence in the blue band. Capable of self-assembly into nanofibers, we have shown we can modulate its aggregation into mesofibers by encapsulation of a small hydrophobic molecule. Conversely, azobenzenes are hydrophobic small molecules that are virtually non-fluorescent in solution due to their highly efficient photoisomerization. However, they demonstrate fluorogenic properties upon confinement in nanoscale assemblies by reducing the non-radiative photoisomerization. Here, we report the fluorescence of a hybrid protein-small molecule system in which azobenzene is confined in our protein assembly leading to fiber thickening and increased fluorescence. We show our engineered protein Q encapsulates AzoCholine, bearing a photoswitchable azobenzene moiety, in the hydrophobic pore to produce fluorescent mesofibers. This study further investigates the photocontrol of protein conformation as well as fluorescence of an azobenze-containing biomaterial. Upon addition of the hydrophobic small molecule, Azocholine, Q is capable of transforming into a fluorescent mesofiber due to fluorogenic encapsulation and fiber thickening.
ISSN:1744-683X
1744-6848
DOI:10.1039/d2sm01578a