Visualizing the in vitro assembly of tropomyosin/actin filaments using TIRF microscopy

Miro Janco, Irina Dedova, Nicole S. Bryce, Edna C. Hardeman, Peter W. Gunning*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

3 Citations (Scopus)

Abstract

Tropomyosins are elongated alpha-helical proteins that form co-polymers with most actin filaments within a cell and play important roles in the structural and functional diversification of the actin cytoskeleton. How the assembly of tropomyosins along an actin filament is regulated and the kinetics of tropomyosin association with an actin filament is yet to be fully determined. A recent series of publications have used total internal reflection fluorescence (TIRF) microscopy in combination with advanced surface and protein chemistry to visualise the molecular assembly of actin/tropomyosin filaments in vitro. Here, we review the use of the in vitro TIRF assay in the determination of kinetic data on tropomyosin filament assembly. This sophisticated approach has enabled generation of real-time single-molecule data to fill the gap between in vitro bulk assays and in vivo assays of tropomyosin function. The in vitro TIRF assays provide a new foundation for future studies involving multiple actin-binding proteins that will more accurately reflect the physiological protein-protein interactions in cells.

Original languageEnglish
Pages (from-to)879-885
Number of pages7
JournalBiophysical Reviews
Volume12
Issue number4
DOIs
Publication statusPublished - Aug 2020
Externally publishedYes

Keywords

  • Actin filaments
  • Actin-binding proteins
  • Intramolecular interactions
  • TIRF microscopy
  • Tropomyosin

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