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

This Article
Right arrow Full Text
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 Fogolari, F.
Right arrow Articles by Viglino, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fogolari, F.
Right arrow Articles by Viglino, P.

Biophys J, January 1999, p. 1-16, Vol. 76, No. 1

Biomolecular Electrostatics with the Linearized Poisson-Boltzmann Equation

Federico Fogolari,* Pierfrancesco Zuccato,*dagger Gennaro Esposito,dagger and Paolo Viglinodagger

 *Dipartimento Scientifico Tecnologico, University of Verona, 37100 Verona, and  dagger Dipartimento di Scienze e Tecnologie Biomediche, Università di Udine, 33100 Udine, Italy

Electrostatics plays a key role in many biological processes. The Poisson-Boltzmann equation (PBE) and its linearized form (LPBE) allow prediction of electrostatic effects for biomolecular systems. The discrepancies between the solutions of the PBE and those of the LPBE are well known for systems with a simple geometry, but much less for biomolecular systems. Results for high charge density systems show that there are limitations to the applicability of the LPBE at low ionic strength and, to a lesser extent, at higher ionic strength. For systems with a simple geometry, the onset of nonlinear effects has been shown to be governed by the ratio of the electric field over the Debye screening constant. This ratio is used in the present work to correct the LPBE results to reproduce fairly accurately those obtained from the PBE for systems with a simple geometry. Since the correction does not involve any geometrical parameter, it can be easily applied to real biomolecular systems. The error on the potential for the LPBE (compared to the PBE) spans few kT/q for the systems studied here and is greatly reduced by the correction. This allows for a more accurate evaluation of the electrostatic free energy of the systems.

Biophys J, January 1999, p. 1-16, Vol. 76, No. 1
© 1999 by the Biophysical Society   0006-3495/99/01/01/16  $2.00



This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
A. Relini, C. Canale, S. De Stefano, R. Rolandi, S. Giorgetti, M. Stoppini, A. Rossi, F. Fogolari, A. Corazza, G. Esposito, et al.
Collagen Plays an Active Role in the Aggregation of beta2-Microglobulin under Physiopathological Conditions of Dialysis-related Amyloidosis
J. Biol. Chem., June 16, 2006; 281(24): 16521 - 16529.
[Abstract] [Full Text] [PDF]


Home page
Protein Sci.Home page
F. Fogolari and S. C.E. Tosatto
Application of MM/PBSA colony free energy to loop decoy discrimination: Toward correlation between energy and root mean square deviation
Protein Sci., April 1, 2005; 14(4): 889 - 901.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
F. Fogolari, A. Brigo, and H. Molinari
Protocol for MM/PBSA Molecular Dynamics Simulations of Proteins
Biophys. J., July 1, 2003; 85(1): 159 - 166.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1999 by the Biophysical Society.