Tunable molecular tension sensors reveal extension-based control of vinculin loading

Elife. 2018 Jul 19:7:e33927. doi: 10.7554/eLife.33927.

Abstract

Molecular tension sensors have contributed to a growing understanding of mechanobiology. However, the limited dynamic range and inability to specify the mechanical sensitivity of these sensors has hindered their widespread use in diverse contexts. Here, we systematically examine the components of tension sensors that can be altered to improve their functionality. Guided by the development of a first principles model describing the mechanical behavior of these sensors, we create a collection of sensors that exhibit predictable sensitivities and significantly improved performance in cellulo. Utilized in the context of vinculin mechanobiology, a trio of these new biosensors with distinct force- and extension-sensitivities reveal that an extension-based control paradigm regulates vinculin loading in a variety of mechanical contexts. To enable the rational design of molecular tension sensors appropriate for diverse applications, we predict the mechanical behavior, in terms of force and extension, of additional 1020 distinct designs.

Keywords: FRET; cell biology; focal adhesion; mechanobiology; molecular biophysics; none; structural biology; tension sensor; vinculin.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amides / pharmacology
  • Amino Acid Sequence
  • Animals
  • Biomechanical Phenomena
  • Biophysical Phenomena
  • Biosensing Techniques*
  • Calibration
  • Fluorescence Resonance Energy Transfer
  • Focal Adhesions / drug effects
  • Focal Adhesions / metabolism
  • HEK293 Cells
  • Humans
  • Luminescent Proteins / chemistry
  • Mice
  • Models, Biological
  • Peptides / metabolism
  • Pyridines / pharmacology
  • Talin / metabolism
  • Vinculin / metabolism*

Substances

  • Amides
  • Luminescent Proteins
  • Peptides
  • Pyridines
  • Talin
  • Vinculin
  • Y 27632