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Portrait of Heiner Linke; Photo: Kennet Ruona

Heiner Linke

Professor, Deputy dean (prorektor) at Faculty of Engineering, LTH

Portrait of Heiner Linke; Photo: Kennet Ruona

Tracking actomyosin at fluorescence check points.


  • Mercy Lard
  • Lasse Ten Siethoff
  • Alf Månsson
  • Heiner Linke

Summary, in English

Emerging concepts for on-chip biotechnologies aim to replace microfluidic flow by active, molecular-motor driven transport of cytoskeletal filaments, including applications in bio-simulation, biocomputation, diagnostics, and drug screening. Many of these applications require reliable detection, with minimal data acquisition, of filaments at many, local checkpoints in a device consisting of a potentially complex network of channels that guide filament motion. Here we develop such a detection system using actomyosin motility. Detection points consist of pairs of gold lines running perpendicular to nanochannels that guide motion of fluorescent actin filaments. Fluorescence interference contrast (FLIC) is used to locally enhance the signal at the gold lines. A cross-correlation method is used to suppress errors, allowing reliable detection of single or multiple filaments. Optimal device design parameters are discussed. The results open for automatic read-out of filament count and velocity in high-throughput motility assays, helping establish the viability of active, motor-driven on-chip applications.


  • Solid State Physics
  • NanoLund: Center for Nanoscience

Publishing year





Scientific Reports



Document type

Journal article


Nature Publishing Group


  • Condensed Matter Physics



Research group

  • Nanometer structure consortium (nmC)


  • ISSN: 2045-2322