Literature DB >> 23291526

Mechanical probes of SOD1 predict systematic trends in metal and dimer affinity of ALS-associated mutants.

Atanu Das1, Steven S Plotkin.   

Abstract

Mutations and oxidative modification in the protein Cu,Zn superoxide dismutase (SOD1) have been implicated in the death of motor neurons in amyotrophic lateral sclerosis (ALS), a presently incurable, invariably fatal neurodegenerative disease. Here we employ steered, all-atom molecular dynamics simulations in implicit solvent to investigate the significance of either mutations or post-translational modifications (PTMs) to SOD1 on metal affinity, dimer stability, and mechanical malleability. The work required to induce moderate structural deformations as a function of sequence index constitutes a "mechanical fingerprint" measuring structural rigidity in the native basin, from which we are able to unambiguously distinguish wild-type SOD1 from PTM variants and measure the severity of a given PTM on structural integrity. The cumulative distribution of work values provided a way to cleanly discriminate between SOD1 variants. Disulfide reduction destabilizes dimer stability more than the removal of either metal, but not moreso than the removal of both metals. Intriguingly, we found that disulfide reduction mechanically stabilizes apo-SOD1 monomer, underscoring the differences between native basin mechanical properties and equilibrium thermodynamic stabilities and elucidating the presence of internal stress in the apo state. All PTMs and ALS-associated mutants studied showed an increased tendency to lose either Cu or Zn and to monomerize-processes known to be critical in the progression of ALS. The valence of Cu strongly modulates its binding free energy. As well, several mutants were more susceptible to loss of metals and monomerization than the disulfide-reduced or apo forms of SOD1. Distance constraints are required to calculate free energies for metal binding and dimer separation, which are validated using thermodynamic cycles. When distance constraints are removed, the results agree with those obtained from direct application of the Jarzynski equality. Crown
Copyright © 2013. Published by Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23291526     DOI: 10.1016/j.jmb.2012.12.022

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  15 in total

1.  Destabilization of the dimer interface is a common consequence of diverse ALS-associated mutations in metal free SOD1.

Authors:  Helen R Broom; Jessica A O Rumfeldt; Kenrick A Vassall; Elizabeth M Meiering
Journal:  Protein Sci       Date:  2015-10-05       Impact factor: 6.725

2.  SOD1 exhibits allosteric frustration to facilitate metal binding affinity.

Authors:  Atanu Das; Steven S Plotkin
Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-19       Impact factor: 11.205

3.  Quantum chemical and molecular mechanics studies on the assessment of interactions between resveratrol and mutant SOD1 (G93A) protein.

Authors:  E Srinivasan; R Rajasekaran
Journal:  J Comput Aided Mol Des       Date:  2018-10-28       Impact factor: 3.686

4.  Molecular mechanisms underlying the impact of mutations in SOD1 on its conformational properties associated with amyotrophic lateral sclerosis as revealed with molecular modelling.

Authors:  Nikolay A Alemasov; Nikita V Ivanisenko; Srinivasan Ramachandran; Vladimir A Ivanisenko
Journal:  BMC Struct Biol       Date:  2018-02-05

Review 5.  Successes and challenges in simulating the folding of large proteins.

Authors:  Anne Gershenson; Shachi Gosavi; Pietro Faccioli; Patrick L Wintrode
Journal:  J Biol Chem       Date:  2019-11-11       Impact factor: 5.157

6.  Interaction between dimer interface residues of native and mutated SOD1 protein: a theoretical study.

Authors:  S P Keerthana; P Kolandaivel
Journal:  J Biol Inorg Chem       Date:  2015-01-13       Impact factor: 3.358

7.  Altered thiol chemistry in human amyotrophic lateral sclerosis-linked mutants of superoxide dismutase 1.

Authors:  Carles Solsona; Thomas B Kahn; Carmen L Badilla; Cristina Álvarez-Zaldiernas; Juan Blasi; Julio M Fernandez; Jorge Alegre-Cebollada
Journal:  J Biol Chem       Date:  2014-08-04       Impact factor: 5.157

8.  A pH Switch Controls Zinc Binding in Tomato Copper-Zinc Superoxide Dismutase.

Authors:  Kevin W Sea; Alexander B Taylor; Susan T Thomas; Amir Liba; Isabelle B Bergman; Stephen P Holloway; Xiaohang Cao; Edith B Gralla; Joan S Valentine; P John Hart; Ahmad Galaleldeen
Journal:  Biochemistry       Date:  2021-05-07       Impact factor: 3.321

Review 9.  Metal-deficient SOD1 in amyotrophic lateral sclerosis.

Authors:  James B Hilton; Anthony R White; Peter J Crouch
Journal:  J Mol Med (Berl)       Date:  2015-03-11       Impact factor: 4.599

10.  Free energy calculations of ALS-causing SOD1 mutants reveal common perturbations to stability and dynamics along the maturation pathway.

Authors:  Nicholas G M Wells; Grant A Tillinghast; Alison L O'Neil; Colin A Smith
Journal:  Protein Sci       Date:  2021-06-22       Impact factor: 6.993

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.