Literature DB >> 15823030

On the charge regulation of proteins.

Mikael Lund1, Bo Jönsson.   

Abstract

It is known that the overall charge of a protein can change as the molecule approaches a charged object like another protein or a cell membrane. We have formalized this mechanism using a statistical mechanical framework and show how this rather overlooked interaction increases the attraction between protein molecules. From the theory, we can identify a unique property, the protein charge capacitance, that contains all information needed to describe the charge regulation mechanism. The capacitance can be obtained from experiment or theory and is a function of pH, salt concentration, and the number of titrating residues. For a range of different protein molecules, we calculate the capacitance and demonstrate how it can be used to quantify the charge regulation interaction. With minimal effort, the derived formulas can be used to improve existing models by including a charge regulation term. Good agreement is found between theory, simulations, and experimental data.

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Year:  2005        PMID: 15823030     DOI: 10.1021/bi047630o

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  22 in total

1.  pK(a) values for the unfolded state under native conditions explain the pH-dependent stability of PGB1.

Authors:  Stina Lindman; Mikael C Bauer; Mikael Lund; Carl Diehl; Frans A A Mulder; Mikael Akke; Sara Linse
Journal:  Biophys J       Date:  2010-11-17       Impact factor: 4.033

2.  pK(a) values for side-chain carboxyl groups of a PGB1 variant explain salt and pH-dependent stability.

Authors:  Stina Lindman; Sara Linse; Frans A A Mulder; Ingemar André
Journal:  Biophys J       Date:  2006-10-13       Impact factor: 4.033

3.  Field-theoretic description of charge regulation interaction.

Authors:  Nataša Adžić; Rudolf Podgornik
Journal:  Eur Phys J E Soft Matter       Date:  2014-06-25       Impact factor: 1.890

4.  pH Dependence of Charge Multipole Moments in Proteins.

Authors:  Anže Lošdorfer Božič; Rudolf Podgornik
Journal:  Biophys J       Date:  2017-10-03       Impact factor: 4.033

Review 5.  Development of constant-pH simulation methods in implicit solvent and applications in biomolecular systems.

Authors:  Fernando Luís Barroso daSilva; Luis Gustavo Dias
Journal:  Biophys Rev       Date:  2017-09-18

6.  Model for evaluating patterned charge-regulation contributions to electrostatic interactions between low-dielectric spheres.

Authors:  Dawn Hollenbeck; K Michael Martini; Andreas Langner; Anthony Harkin; David S Ross; George M Thurston
Journal:  Phys Rev E Stat Nonlin Soft Matter Phys       Date:  2010-09-07

7.  Salt enhances calmodulin-target interaction.

Authors:  Ingemar André; Tõnu Kesvatera; Bo Jönsson; Sara Linse
Journal:  Biophys J       Date:  2006-01-20       Impact factor: 4.033

8.  Charge-regulation phase transition on surface lattices of titratable sites adjacent to electrolyte solutions: An analog of the Ising antiferromagnet in a magnetic field.

Authors:  Joel D Shore; George M Thurston
Journal:  Phys Rev E Stat Nonlin Soft Matter Phys       Date:  2015-12-14

9.  Toward optimized potential functions for protein-protein interactions in aqueous solutions: osmotic second virial coefficient calculations using the MARTINI coarse-grained force field.

Authors:  Austin C Stark; Casey T Andrews; Adrian H Elcock
Journal:  J Chem Theory Comput       Date:  2013-09-10       Impact factor: 6.006

10.  Model for screened, charge-regulated electrostatics of an eye lens protein: Bovine gammaB-crystallin.

Authors:  Christopher W Wahle; K Michael Martini; Dawn M Hollenbeck; Andreas Langner; David S Ross; John F Hamilton; George M Thurston
Journal:  Phys Rev E       Date:  2017-09-25       Impact factor: 2.529

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