Reversible Photocontrol of Microtubule Stability by Spiropyran-Conjugated Tau-Derived Peptides

Chembiochem. 2023 Apr 17;24(8):e202200782. doi: 10.1002/cbic.202200782. Epub 2023 Mar 29.

Abstract

Spatiotemporal modulation of microtubules by light has become an important aspect of the biological and nanotechnological applications of microtubules. We previously developed a Tau-derived peptide as a binding unit to the inside of microtubules. Here, we conjugated the Tau-derived peptide to spiropyran, which is reversibly converted to merocyanine by light, as a reversible photocontrol system to stabilize microtubules. Among the synthesized peptides with spiropyran/merocyanine at different positions, several peptides were bound to the inside of microtubules and stabilized the structures of microtubules. The peptide with spiropyran at the N-terminus induced polymerization and stabilization of microtubules, whereas the same peptide with the merocyanine form did not exert these effects. Reversible formation of microtubules/tubulin aggregates was achieved using the peptide with spiropyran conjugated at the N-terminus and irradiation with UV and visible light. Spiropyran-conjugated Tau-derived peptides would be useful for spatiotemporal modulation of microtubule stability through reversible photocontrol of binding.

Keywords: Tau-derived peptide; microtubules; photoisomerization; spiropyran; supramolecular chemistry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzopyrans / chemistry
  • Microtubules*
  • Peptides / chemistry
  • Tubulin* / metabolism
  • tau Proteins / metabolism

Substances

  • spiropyran
  • Tubulin
  • Peptides
  • Benzopyrans
  • tau Proteins