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

Biophysical Journal 53: 593-607 (1988)
© 1988 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 Bentz, J
Right arrow Articles by Düzgünes, N
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bentz, J
Right arrow Articles by Düzgünes, N

La3+-induced fusion of phosphatidylserine liposomes. Close approach, intermembrane intermediates, and the electrostatic surface potential.

J Bentz, D Alford, J Cohen and N Düzgünes

Department of Pharmacy, School of Pharmacy, University of California, San Francisco 94143.

ABSTRACT

The fusion of large unilamellar phosphatidylserine liposomes (PS LUV) induced by La3+ has been monitored using the 1-aminoapthalene-3,6,8-trisulfonic acid/p-xylenebis(pyridinium bromide) (ANTS/DPX) fluorescence assay for the mixing of aqueous contents. The fusion event is extensive and nonleaky, with up to 95% mixing of contents in the fused liposomes. However, addition of excess EDTA leads to disruption of the fusion products in a way that implies the existence of metastable intermembrane contact sites. The maximal fusion activity occurs between 10 and 100 microM La3+ and fusion can be terminated rapidly, without loss of contents, by the addition of excess La3+, e.g., 1 mM La3+ at pH 7.4. This observation is explained by the very large intrinsic binding constant (approximately 10(5) M-1) of La3+ to the PS headgroup, as measured by microelectrophoresis. Addition of 1 mM La3+ causes charge reversal of the membrane and a large positive surface potential. La3+ binding to PS causes the release of a proton. These data can be explained if La3+ can chelate to PS at two sites, with one of the sites being the primary amino group. This binding model successfully predicts that at pH 4.5 fusion occurs up to 2 mM La3+, due to reduced La3+ binding at low pH. We conclude that the general mechanism of membrane fusion includes three kinetic steps. In addition to (a) aggregation, there is (b) the close approach of the surfaces, or thinning of the hydration layer, and (c) the formation of intermembrane intermediates which determine the extent to which membrane destabilization leads to fusion (mixing of aqueous contents), as opposed to lysis. The lifetime of these intermembrane intermediates appears to depend upon La3+ binding to both PS sites.




This article has been cited by other articles:


Home page
Biophys. JHome page
D. J. Estes, S. R. Lopez, A. O. Fuller, and M. Mayer
Triggering and Visualizing the Aggregation and Fusion of Lipid Membranes in Microfluidic Chambers
Biophys. J., July 1, 2006; 91(1): 233 - 243.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
L. J. Siskind, A. Davoody, N. Lewin, S. Marshall, and M. Colombini
Enlargement and Contracture of C2-Ceramide Channels
Biophys. J., September 1, 2003; 85(3): 1560 - 1575.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
L. Yang and H. W. Huang
Observation of a Membrane Fusion Intermediate Structure
Science, September 13, 2002; 297(5588): 1877 - 1879.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
F. Boudreault and R. Grygorczyk
Cell swelling-induced ATP release and gadolinium-sensitive channels
Am J Physiol Cell Physiol, January 1, 2002; 282(1): C219 - C226.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1988 by the Biophysical Society.