Literature DB >> 23729910

Role of methyl groups in dynamics and evolution of biomolecules.

Jonathan D Nickels1, Joseph E Curtis, Hugh O'Neill, Alexei P Sokolov.   

Abstract

Recent studies have discovered strong differences between the dynamics of nucleic acids (RNA and DNA) and proteins, especially at low hydration and low temperatures. This difference is caused primarily by dynamics of methyl groups that are abundant in proteins, but are absent or very rare in RNA and DNA. In this paper, we present a hypothesis regarding the role of methyl groups as intrinsic plasticizers in proteins and their evolutionary selection to facilitate protein dynamics and activity. We demonstrate the profound effect methyl groups have on protein dynamics relative to nucleic acid dynamics, and note the apparent correlation of methyl group content in protein classes and their need for molecular flexibility. Moreover, we note the fastest methyl groups of some enzymes appear around dynamical centers such as hinges or active sites. Methyl groups are also of tremendous importance from a hydrophobicity/folding/entropy perspective. These significant roles, however, complement our hypothesis rather than preclude the recognition of methyl groups in the dynamics and evolution of biomolecules.Electronic supplementary material The online version of this article (doi:10.1007/s10867-012-9268-6) contains supplementary material, which is available to authorized users.

Keywords:  Nucleic acid dynamics; Protein dynamics; RNA dynamics; RNA world

Year:  2012        PMID: 23729910      PMCID: PMC3388196          DOI: 10.1007/s10867-012-9268-6

Source DB:  PubMed          Journal:  J Biol Phys        ISSN: 0092-0606            Impact factor:   1.365


  19 in total

1.  Dynamics of biological macromolecules: not a simple slaving by hydration water.

Authors:  S Khodadadi; J H Roh; A Kisliuk; E Mamontov; M Tyagi; S A Woodson; R M Briber; A P Sokolov
Journal:  Biophys J       Date:  2010-04-07       Impact factor: 4.033

2.  Onsets of anharmonicity in protein dynamics.

Authors:  J H Roh; V N Novikov; R B Gregory; J E Curtis; Z Chowdhuri; A P Sokolov
Journal:  Phys Rev Lett       Date:  2005-07-12       Impact factor: 9.161

3.  Dynamic transition in tRNA is solvent induced.

Authors:  Gokhan Caliskan; Robert M Briber; D Thirumalai; Victoria Garcia-Sakai; Sarah A Woodson; Alexei P Sokolov
Journal:  J Am Chem Soc       Date:  2006-01-11       Impact factor: 15.419

4.  Dynamics of tRNA at different levels of hydration.

Authors:  J H Roh; R M Briber; A Damjanovic; D Thirumalai; S A Woodson; A P Sokolov
Journal:  Biophys J       Date:  2009-04-08       Impact factor: 4.033

5.  Barstar has a highly dynamic hydrophobic core: evidence from molecular dynamics simulations and nuclear magnetic resonance relaxation data.

Authors:  K B Wong; V Daggett
Journal:  Biochemistry       Date:  1998-08-11       Impact factor: 3.162

6.  Freezing of dynamics of a methyl group in a protein hydrophobic core at cryogenic temperatures by deuteron NMR spectroscopy.

Authors:  Liliya Vugmeyster; Dmitry Ostrovsky; Joseph J Ford; Andrew S Lipton
Journal:  J Am Chem Soc       Date:  2010-03-31       Impact factor: 15.419

7.  Slow relaxation process in DNA.

Authors:  A P Sokolov; H Grimm; A Kisliuk; A J Dianoux
Journal:  J Biol Phys       Date:  2001-12       Impact factor: 1.365

8.  The RNA moiety of ribonuclease P is the catalytic subunit of the enzyme.

Authors:  C Guerrier-Takada; K Gardiner; T Marsh; N Pace; S Altman
Journal:  Cell       Date:  1983-12       Impact factor: 41.582

9.  Role of domain 3 of calmodulin in activation of calmodulin-stimulated phosphodiesterase and smooth muscle myosin light chain kinase.

Authors:  Z Su; D Fan; S E George
Journal:  J Biol Chem       Date:  1994-06-17       Impact factor: 5.157

10.  Observation of a low-temperature, dynamically driven structural transition in a polypeptide by solid-state NMR spectroscopy.

Authors:  Vikram S Bajaj; Patrick C A van der Wel; Robert G Griffin
Journal:  J Am Chem Soc       Date:  2009-01-14       Impact factor: 15.419

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  4 in total

1.  Coherent neutron scattering and collective dynamics in the protein, GFP.

Authors:  Jonathan D Nickels; Stefania Perticaroli; Hugh O'Neill; Qiu Zhang; Georg Ehlers; Alexei P Sokolov
Journal:  Biophys J       Date:  2013-11-05       Impact factor: 4.033

2.  Dynamics of protein and its hydration water: neutron scattering studies on fully deuterated GFP.

Authors:  Jonathan D Nickels; Hugh O'Neill; Liang Hong; Madhusudan Tyagi; Georg Ehlers; Kevin L Weiss; Qiu Zhang; Zheng Yi; Eugene Mamontov; Jeremy C Smith; Alexei P Sokolov
Journal:  Biophys J       Date:  2012-10-02       Impact factor: 4.033

3.  Structural effects of modified ribonucleotides and magnesium in transfer RNAs.

Authors:  You Xu; Alexander D MacKerell; Lennart Nilsson
Journal:  Bioorg Med Chem       Date:  2016-06-18       Impact factor: 3.641

Review 4.  Water in protein hydration and ligand recognition.

Authors:  Manuela Maurer; Chris Oostenbrink
Journal:  J Mol Recognit       Date:  2019-08-27       Impact factor: 2.891

  4 in total

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