Molecular viewing of actin polymerizing actions and beyond: combination analysis of single-molecule speckle microscopy with modeling, FRAP and s-FDAP (sequential fluorescence decay after photoactivation)

Dev Growth Differ. 2013 May;55(4):508-14. doi: 10.1111/dgd.12060. Epub 2013 Apr 29.

Abstract

Live-cell single-molecule imaging is a powerful tool to elucidate the in vivo biochemistry of cytoskeletal proteins. However, it is often somewhat difficult to interpret how a bulk population of the observed molecule might behave as a whole. We review our recent studies in which the combination of image analysis with modeling and bulk kinetics measurements such as FRAP (fluorescence recovery after photobleaching) clarified basic problems in the regulation of actin remodeling pathways.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Actins / chemistry*
  • Cytoskeleton / metabolism
  • Fluorescence Recovery After Photobleaching / methods*
  • Image Processing, Computer-Assisted
  • Microscopy / methods*
  • Molecular Imaging / methods
  • Pseudopodia / metabolism

Substances

  • Actins