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

Biophysical Journal 58: 577-583 (1990)
© 1990 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 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 Schwarz, G.
Right arrow Articles by Robert, C. H.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Schwarz, G.
Right arrow Articles by Robert, C. H.

Pore formation kinetics in membranes, determined from the release of marker molecules out of liposomes or cells

Gerhard Schwarz and Charles H. Robert

Department of Biophysical Chemistry, Biocenter of the University, CH-4056 Basel, Switzerland

ABSTRACT

We discuss the efflux of entrapped marker material from liposomes or cells through pores in the membrane, being monitored by the time course of a certain signal F (e.g., fluorescence emission). This is expressed in terms of an appropriate normalized function of time, the so-called efflux function E(t). Under conditions frequently encountered in practice the measured E(t) can be easily related to the forward rate of pore formation if the liposomes/cells are monodisperse in size. In the basic case of a time-independent rate law it turns out that E(t) must be single exponential. Deviations from such a simple functional behavior might be due to a fairly broad distribution of liposome/cell sizes and/or a more complicated pore formation mechanism. A relevant evaluation of original data is demonstrated making use of experimental results obtained with small unilamellar lipid vesicles where pores are induced by the antibiotic peptide alamethicin. This includes the application of a general method to eliminate the effect of a given liposome/cell size distribution.




This article has been cited by other articles:


Home page
Biophys. JHome page
L. Silva, A. Coutinho, A. Fedorov, and M. Prieto
Competitive Binding of Cholesterol and Ergosterol to the Polyene Antibiotic Nystatin. A Fluorescence Study
Biophys. J., May 15, 2006; 90(10): 3625 - 3631.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
A. Coutinho, L. Silva, A. Fedorov, and M. Prieto
Cholesterol and Ergosterol Influence Nystatin Surface Aggregation: Relation to Pore Formation
Biophys. J., November 1, 2004; 87(5): 3264 - 3276.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
L. R. Montes, M. B. Ruiz-Arguello, F. M. Goni, and A. Alonso
Membrane Restructuring via Ceramide Results in Enhanced Solute Efflux
J. Biol. Chem., March 29, 2002; 277(14): 11788 - 11794.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1990 by the Biophysical Society.