Literature DB >> 18757562

Influence of macromolecular crowding on protein-protein association rates--a Brownian dynamics study.

Grzegorz Wieczorek1, Piotr Zielenkiewicz.   

Abstract

The high total concentration of macromolecules, often referred to as macromolecular crowding, is one of the characteristic features of living cells. Macromolecular crowding influences interactions between many types of macromolecules, with consequent effects on, among others, the rates of reactions occurring in the cell. Simulations to study the influence of crowding on macromolecular association rate were performed using a modified Brownian dynamics protocol. The calculated values of the time-dependent self-diffusion coefficients in different crowding conditions are in a very good agreement with those obtained by other authors. Simulations of the complex formation between the monoclonal antibody HyHEL-5 and its antigen hen egg lysozyme, both represented at atomic level detail, show that the calculated association rates strongly depend on the volume excluded by crowding. The rate obtained for the highest concentration of crowding particles is greater than twofold higher than the rate for proteins without crowding.

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Year:  2008        PMID: 18757562      PMCID: PMC2586562          DOI: 10.1529/biophysj.108.136291

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  32 in total

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Journal:  Biophys J       Date:  1999-12       Impact factor: 4.033

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Authors:  A P Minton
Journal:  J Biol Chem       Date:  2001-02-15       Impact factor: 5.157

Review 3.  Macromolecular crowding: an important but neglected aspect of the intracellular environment.

Authors:  R J Ellis
Journal:  Curr Opin Struct Biol       Date:  2001-02       Impact factor: 6.809

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Authors:  G Rivas; J A Fernández; A P Minton
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-13       Impact factor: 11.205

5.  Protein-protein association: investigation of factors influencing association rates by brownian dynamics simulations.

Authors:  R R Gabdoulline; R C Wade
Journal:  J Mol Biol       Date:  2001-03-09       Impact factor: 5.469

6.  Excluded volume effects on the refolding and assembly of an oligomeric protein. GroEL, a case study.

Authors:  A Galan; B Sot; O Llorca; J L Carrascosa; J M Valpuesta; A Muga
Journal:  J Biol Chem       Date:  2001-01-12       Impact factor: 5.157

7.  Electrostatic analysis and Brownian dynamics simulation of the association of plastocyanin and cytochrome f.

Authors:  F De Rienzo; R R Gabdoulline; M C Menziani; P G De Benedetti; R C Wade
Journal:  Biophys J       Date:  2001-12       Impact factor: 4.033

Review 8.  Kinetic studies of protein-protein interactions.

Authors:  Gideon Schreiber
Journal:  Curr Opin Struct Biol       Date:  2002-02       Impact factor: 6.809

Review 9.  Macromolecular crowding: obvious but underappreciated.

Authors:  R J Ellis
Journal:  Trends Biochem Sci       Date:  2001-10       Impact factor: 13.807

10.  Molecular crowding enhances native structure and stability of alpha/beta protein flavodoxin.

Authors:  Loren Stagg; Shao-Qing Zhang; Margaret S Cheung; Pernilla Wittung-Stafshede
Journal:  Proc Natl Acad Sci U S A       Date:  2007-11-16       Impact factor: 11.205

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  38 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-17       Impact factor: 11.205

2.  Crowding effects on association reactions at membranes.

Authors:  Jun Soo Kim; Arun Yethiraj
Journal:  Biophys J       Date:  2010-03-17       Impact factor: 4.033

3.  Absolute protein-protein association rate constants from flexible, coarse-grained Brownian dynamics simulations: the role of intermolecular hydrodynamic interactions in barnase-barstar association.

Authors:  Tamara Frembgen-Kesner; Adrian H Elcock
Journal:  Biophys J       Date:  2010-11-03       Impact factor: 4.033

4.  Brownian dynamics simulation of protein solutions: structural and dynamical properties.

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Journal:  Biophys J       Date:  2010-12-01       Impact factor: 4.033

5.  Macromolecular crowding induces polypeptide compaction and decreases folding cooperativity.

Authors:  Douglas Tsao; Nikolay V Dokholyan
Journal:  Phys Chem Chem Phys       Date:  2010-04-14       Impact factor: 3.676

6.  Power-law dependence of the melting temperature of ubiquitin on the volume fraction of macromolecular crowders.

Authors:  Matthias M Waegele; Feng Gai
Journal:  J Chem Phys       Date:  2011-03-07       Impact factor: 3.488

Review 7.  Understanding biochemical processes in the presence of sub-diffusive behavior of biomolecules in solution and living cells.

Authors:  Sujit Basak; Sombuddha Sengupta; Krishnananda Chattopadhyay
Journal:  Biophys Rev       Date:  2019-08-23

8.  Protein charge and mass contribute to the spatio-temporal dynamics of protein-protein interactions in a minimal proteome.

Authors:  Yu Xu; Hong Wang; Ruth Nussinov; Buyong Ma
Journal:  Proteomics       Date:  2013-03-18       Impact factor: 3.984

9.  Hydrophilicity matching - a potential prerequisite for the formation of protein-protein complexes in the cell.

Authors:  Mario Hlevnjak; Gordan Zitkovic; Bojan Zagrovic
Journal:  PLoS One       Date:  2010-06-17       Impact factor: 3.240

10.  Diffusion, crowding & protein stability in a dynamic molecular model of the bacterial cytoplasm.

Authors:  Sean R McGuffee; Adrian H Elcock
Journal:  PLoS Comput Biol       Date:  2010-03-05       Impact factor: 4.475

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