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A comparative study of cold-and warmadapted Endonucleases A using sequence analyses and molecular Dynamics simulations

Permanent lenke
https://hdl.handle.net/10037/12140
DOI
https://doi.org/10.1371/journal.pone.0169586
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article.pdf (2.391Mb)
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Dato
2017-02-13
Type
Journal article
Tidsskriftartikkel
Peer reviewed
Article has an altmetric score of 2
Forfatter
Michetti, Davide; Brandsdal, Bjørn Olav; Bon, Davide; Isaksen, Geir Villy; Tiberti, Matteo; Papaleo, Elena
Sammendrag
The psychrophilic and mesophilic endonucleases A (EndA) from Aliivibrio salmonicida (VsEndA) and Vibrio cholera (VcEndA) have been studied experimentally in terms of the biophysical properties related to thermal adaptation. The analyses of their static X-ray structures was no sufficient to rationalize the determinants of their adaptive traits at the molecular level. Thus, we used Molecular Dynamics (MD) simulations to compare the two proteins and unveil their structural and dynamical differences. Our simulations did not show a substantial increase in flexibility in the cold-adapted variant on the nanosecond time scale. The only exception is a more rigid C-terminal region in VcEndA, which is ascribable to a cluster of electrostatic interactions and hydrogen bonds, as also supported by MD simulations of the VsEndA mutant variant where the cluster of interactions was introduced. Moreover, we identified three additional amino acidic substitutions through multiple sequence alignment and the analyses of MD-based protein structure networks. In particular, T120V occurs in the proximity of the catalytic residue H80 and alters the interaction with the residue Y43, which belongs to the second coordination sphere of the Mg2+ ion. This makes T120V an amenable candidate for future experimental mutagenesis.
Forlag
Public Library of Science
Sitering
Michetti, D., Brandsdal, B.O., Bon, D., Isaksen, G.V., Tiberti, M., Papaleo, E. A comparative study of cold-and warmadapted Endonucleases A using sequence analyses and molecular Dynamics simulations. PLoS ONE. 2017;12:e0169586(2):1-18
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