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Bluues: a program for the analysis of the electrostatic properties of proteins based on generalized Born radii
BACKGROUND: The Poisson-Boltzmann (PB) equation and its linear approximation have been widely used to describe biomolecular electrostatics. Generalized Born (GB) models offer a convenient computational approximation for the more fundamental approach based on the Poisson-Boltzmann equation, and allow...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434445/ https://www.ncbi.nlm.nih.gov/pubmed/22536964 http://dx.doi.org/10.1186/1471-2105-13-S4-S18 |
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author | Fogolari, Federico Corazza, Alessandra Yarra, Vijaylakshmi Jalaru, Anusha Viglino, Paolo Esposito, Gennaro |
author_facet | Fogolari, Federico Corazza, Alessandra Yarra, Vijaylakshmi Jalaru, Anusha Viglino, Paolo Esposito, Gennaro |
author_sort | Fogolari, Federico |
collection | PubMed |
description | BACKGROUND: The Poisson-Boltzmann (PB) equation and its linear approximation have been widely used to describe biomolecular electrostatics. Generalized Born (GB) models offer a convenient computational approximation for the more fundamental approach based on the Poisson-Boltzmann equation, and allows estimation of pairwise contributions to electrostatic effects in the molecular context. RESULTS: We have implemented in a single program most common analyses of the electrostatic properties of proteins. The program first computes generalized Born radii, via a surface integral and then it uses generalized Born radii (using a finite radius test particle) to perform electrostic analyses. In particular the ouput of the program entails, depending on user's requirement: 1) the generalized Born radius of each atom; 2) the electrostatic solvation free energy; 3) the electrostatic forces on each atom (currently in a dvelopmental stage); 4) the pH-dependent properties (total charge and pH-dependent free energy of folding in the pH range -2 to 18; 5) the pKa of all ionizable groups; 6) the electrostatic potential at the surface of the molecule; 7) the electrostatic potential in a volume surrounding the molecule; CONCLUSIONS: Although at the expense of limited flexibility the program provides most common analyses with requirement of a single input file in PQR format. The results obtained are comparable to those obtained using state-of-the-art Poisson-Boltzmann solvers. A Linux executable with example input and output files is provided as supplementary material. |
format | Online Article Text |
id | pubmed-3434445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34344452012-09-06 Bluues: a program for the analysis of the electrostatic properties of proteins based on generalized Born radii Fogolari, Federico Corazza, Alessandra Yarra, Vijaylakshmi Jalaru, Anusha Viglino, Paolo Esposito, Gennaro BMC Bioinformatics Research BACKGROUND: The Poisson-Boltzmann (PB) equation and its linear approximation have been widely used to describe biomolecular electrostatics. Generalized Born (GB) models offer a convenient computational approximation for the more fundamental approach based on the Poisson-Boltzmann equation, and allows estimation of pairwise contributions to electrostatic effects in the molecular context. RESULTS: We have implemented in a single program most common analyses of the electrostatic properties of proteins. The program first computes generalized Born radii, via a surface integral and then it uses generalized Born radii (using a finite radius test particle) to perform electrostic analyses. In particular the ouput of the program entails, depending on user's requirement: 1) the generalized Born radius of each atom; 2) the electrostatic solvation free energy; 3) the electrostatic forces on each atom (currently in a dvelopmental stage); 4) the pH-dependent properties (total charge and pH-dependent free energy of folding in the pH range -2 to 18; 5) the pKa of all ionizable groups; 6) the electrostatic potential at the surface of the molecule; 7) the electrostatic potential in a volume surrounding the molecule; CONCLUSIONS: Although at the expense of limited flexibility the program provides most common analyses with requirement of a single input file in PQR format. The results obtained are comparable to those obtained using state-of-the-art Poisson-Boltzmann solvers. A Linux executable with example input and output files is provided as supplementary material. BioMed Central 2012-03-28 /pmc/articles/PMC3434445/ /pubmed/22536964 http://dx.doi.org/10.1186/1471-2105-13-S4-S18 Text en Copyright ©2012 Fogolari et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Fogolari, Federico Corazza, Alessandra Yarra, Vijaylakshmi Jalaru, Anusha Viglino, Paolo Esposito, Gennaro Bluues: a program for the analysis of the electrostatic properties of proteins based on generalized Born radii |
title | Bluues: a program for the analysis of the electrostatic properties of proteins based on generalized Born radii |
title_full | Bluues: a program for the analysis of the electrostatic properties of proteins based on generalized Born radii |
title_fullStr | Bluues: a program for the analysis of the electrostatic properties of proteins based on generalized Born radii |
title_full_unstemmed | Bluues: a program for the analysis of the electrostatic properties of proteins based on generalized Born radii |
title_short | Bluues: a program for the analysis of the electrostatic properties of proteins based on generalized Born radii |
title_sort | bluues: a program for the analysis of the electrostatic properties of proteins based on generalized born radii |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434445/ https://www.ncbi.nlm.nih.gov/pubmed/22536964 http://dx.doi.org/10.1186/1471-2105-13-S4-S18 |
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