help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Biophysical Journal 71: 1228-1234 (1996)
© 1996 the Biophysical Society

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Janson, L W
Right arrow Articles by Luby-Phelps, K
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Janson, L W
Right arrow Articles by Luby-Phelps, K

Mechanism and size cutoff for steric exclusion from actin-rich cytoplasmic domains.

L W Janson, K Ragsdale and K Luby-Phelps

University of Texas Southwestern Medical Center at Dallas 75235-9040, USA.

ABSTRACT

Subdomains of the cytoplasmic volume in tissue culture cells exclude large tracer particles relative to small. Evidence suggests that exclusion of the large particles is due to molecular sieving by the dense meshwork of microfilaments found in these compartments, but exclusion as a result of the close apposition of the dorsal and ventral plasma membrane of the cell in these regions has not been ruled out conclusively. In principle, these two mechanisms can be distinguished by the dependence of exclusion on tracer particle size. By fluorescence ratio imaging we have measured the partition coefficient (P/PO) into excluding compartments for tracer particles ranging in radius from 1 to 41 nm. The decay of P/PO as a function of particle radius is better fitted by three molecular sieving models than by a slit pore model. The sieving models predict a percolation cutoff radius of the order of 50 nm for partitioning into excluding compartments.




This article has been cited by other articles:


Home page
J. Cell Sci.Home page
J. A. Peet, A. Bragin, P. D. Calvert, S. S. Nikonov, S. Mani, X. Zhao, J. C. Besharse, E. A. Pierce, B. E. Knox, and E. N. Pugh Jr
Quantification of the cytoplasmic spaces of living cells with EGFP reveals arrestin-EGFP to be in disequilibrium in dark adapted rod photoreceptors
J. Cell Sci., June 15, 2004; 117(14): 3049 - 3059.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
S. T. Kinsey and T. S. Moerland
Metabolite diffusion in giant muscle fibers of the spiny lobster Panulirus argus
J. Exp. Biol., November 1, 2002; 205(21): 3377 - 3386.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Biol.Home page
W. Christian Wigley, R. P. Fabunmi, M. G. Lee, C. R. Marino, S. Muallem, G. N. DeMartino, and P. J. Thomas
Dynamic Association of Proteasomal Machinery with the Centrosome
J. Cell Biol., May 3, 1999; 145(3): 481 - 490.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
J. C. Politz, E. S. Browne, D. E. Wolf, and T. Pederson
Intranuclear diffusion and hybridization state of oligonucleotides measured by fluorescence correlation spectroscopy in living cells
PNAS, May 26, 1998; 95(11): 6043 - 6048.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1996 by the Biophysical Society.