Stoichiometry of molecular complexes at adhesions in living cells
570
Cytoplasm
Image Processing
brightness analysis
confocal microscopy
Models, Biological
Fluorescence
Mice
03 medical and health sciences
Computer-Assisted
Models
Cell Movement
Cell Adhesion
Image Processing, Computer-Assisted
2.1 Biological and endogenous factors
Animals
Microscopy
0303 health sciences
Models, Statistical
cross-correlation
Biological Sciences
Statistical
Fibroblasts
Biological
Vinculin
Microscopy, Fluorescence
Focal Adhesion Protein-Tyrosine Kinases
Biochemistry and Cell Biology
Paxillin
DOI:
10.1073/pnas.0806036106
Publication Date:
2009-01-24T01:54:40Z
AUTHORS (5)
ABSTRACT
We describe a method to detect molecular complexes and measure their stoichiometry in living cells from simultaneous fluctuations of the fluorescence intensity in two image channels, each detecting a different kind of protein. The number and brightness (N&B) analysis, namely, the use of the ratio between the variance and the average intensity to obtain the brightness of molecules, is extended to the cross-variance of the intensity fluctuations in two channels. We apply the cross-variance method to determine the stoichiometry of complexes containing paxillin and vinculin or focal adhesion kinase (FAK) in disassembling adhesions in mouse embryo fibroblasts expressing FAK, vinculin, and paxillin-tagged with EGFP and mCherry. We found no complexes of these proteins in the cytoplasm away from the adhesions. However, at the adhesions, large aggregates leave, forming a hole, during their disassembly. This hole shows cross-correlation between FAK and paxillin and vinculin and paxillin. From the amplitude of the correlated fluctuations we determine the composition of the aggregates leaving the adhesions. These aggregates disassemble rapidly in the cytoplasm because large complexes are found only in very close proximity to the adhesions or at their borders.
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