Mass-sensitive particle tracking to elucidate the membrane-associated MinDE reaction cycle

Nat Methods. 2021 Oct;18(10):1239-1246. doi: 10.1038/s41592-021-01260-x. Epub 2021 Oct 4.

Abstract

In spite of their great importance in biology, methods providing access to spontaneous molecular interactions with and on biological membranes have been sparse. The recent advent of mass photometry to quantify mass distributions of unlabeled biomolecules landing on surfaces raised hopes that this approach could be transferred to membranes. Here, by introducing a new interferometric scattering (iSCAT) image processing and analysis strategy adapted to diffusing particles, we enable mass-sensitive particle tracking (MSPT) of single unlabeled biomolecules on a supported lipid bilayer. We applied this approach to the highly nonlinear reaction cycles underlying MinDE protein self-organization. MSPT allowed us to determine the stoichiometry and turnover of individual membrane-bound MinD/MinDE protein complexes and to quantify their size-dependent diffusion. This study demonstrates the potential of MSPT to enhance our quantitative understanding of membrane-associated biological systems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / chemistry
  • Adenosine Triphosphatases / metabolism*
  • Biophysical Phenomena*
  • Cell Cycle Proteins / chemistry
  • Cell Cycle Proteins / metabolism*
  • Cell Membrane / metabolism
  • Cell Membrane / physiology*
  • Escherichia coli
  • Escherichia coli Proteins / chemistry
  • Escherichia coli Proteins / metabolism*
  • Lipid Bilayers / chemistry
  • Lipid Bilayers / metabolism*

Substances

  • Cell Cycle Proteins
  • Escherichia coli Proteins
  • Lipid Bilayers
  • MinE protein, E coli
  • Adenosine Triphosphatases
  • MinD protein, E coli