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Pregled bibliografske jedinice broj: 544524

Intrinsically Disordered Regions May Lower the Hydration Free Energy in Proteins: A Case Study of Nudix Hydrolase in the Bacterium Deinococcus radiodurans


Awile, Omar; Kriško, Anita; Sbalzarini, Ivo; Žagrović, Bojan
Intrinsically Disordered Regions May Lower the Hydration Free Energy in Proteins: A Case Study of Nudix Hydrolase in the Bacterium Deinococcus radiodurans // Plos computational biology, 6 (2010), 7; 1-10 doi:10.1371/journal.pcbi.1000854 (međunarodna recenzija, članak, znanstveni)


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Naslov
Intrinsically Disordered Regions May Lower the Hydration Free Energy in Proteins: A Case Study of Nudix Hydrolase in the Bacterium Deinococcus radiodurans

Autori
Awile, Omar ; Kriško, Anita ; Sbalzarini, Ivo ; Žagrović, Bojan

Izvornik
Plos computational biology (1553-734X) 6 (2010), 7; 1-10

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
D. radiodurans; disordered proteins; nudix hydrolase; desiccation effects; radiation-resistant

Sažetak
The proteome of the radiation- and desiccation-resistant bacterium D. radiodurans features a group of proteins that contain significant intrinsically disordered regions that are not present in non-extremophile homologues. Interestingly, this group includes a number of housekeeping and repair proteins such as DNA polymerase III, nudix hydrolase and rotamase. Here, we focus on a member of the nudix hydrolase family from D. radiodurans possessing low-complexity N- and C-terminal tails, which exhibit sequence signatures of intrinsic disorder and have unknown function. The enzyme catalyzes the hydrolysis of oxidatively damaged and mutagenic nucleotides, and it is thought to play an important role in D. radiodurans during the recovery phase after exposure to ionizing radiation or desiccation. We use molecular dynamics simulations to study the dynamics of the protein, and study its hydration free energy using the GB/SA formalism. We show that the presence of disordered tails significantly decreases the hydration free energy of the whole protein. We hypothesize that the tails increase the chances of the protein to be located in the remaining water patches in the desiccated cell, where it is protected from the desiccation effects and can function normally. We extrapolate this to other intrinsically disordered regions in proteins, and propose a novel function for them: intrinsically disordered regions increase the "surface-properties" of the folded domains they are attached to, making them on the whole more hydrophilic and potentially influencing, in this way, their localization and cellular activity.

Izvorni jezik
Engleski

Znanstvena područja
Fizika, Kemija, Biologija



POVEZANOST RADA


Projekti:
177-1770495-0476 - Razvoj i primjene principa maksimalne proizvodnje entropije (Juretić, Davor, MZOS ) ( CroRIS)

Ustanove:
Prirodoslovno-matematički fakultet, Split

Profili:

Avatar Url Bojan Žagrović (autor)

Avatar Url Anita Kriško (autor)

Poveznice na cjeloviti tekst rada:

doi www.ploscompbiol.org

Citiraj ovu publikaciju:

Awile, Omar; Kriško, Anita; Sbalzarini, Ivo; Žagrović, Bojan
Intrinsically Disordered Regions May Lower the Hydration Free Energy in Proteins: A Case Study of Nudix Hydrolase in the Bacterium Deinococcus radiodurans // Plos computational biology, 6 (2010), 7; 1-10 doi:10.1371/journal.pcbi.1000854 (međunarodna recenzija, članak, znanstveni)
Awile, O., Kriško, A., Sbalzarini, I. & Žagrović, B. (2010) Intrinsically Disordered Regions May Lower the Hydration Free Energy in Proteins: A Case Study of Nudix Hydrolase in the Bacterium Deinococcus radiodurans. Plos computational biology, 6 (7), 1-10 doi:10.1371/journal.pcbi.1000854.
@article{article, author = {Awile, Omar and Kri\v{s}ko, Anita and Sbalzarini, Ivo and \v{Z}agrovi\'{c}, Bojan}, year = {2010}, pages = {1-10}, DOI = {10.1371/journal.pcbi.1000854}, keywords = {D. radiodurans, disordered proteins, nudix hydrolase, desiccation effects, radiation-resistant}, journal = {Plos computational biology}, doi = {10.1371/journal.pcbi.1000854}, volume = {6}, number = {7}, issn = {1553-734X}, title = {Intrinsically Disordered Regions May Lower the Hydration Free Energy in Proteins: A Case Study of Nudix Hydrolase in the Bacterium Deinococcus radiodurans}, keyword = {D. radiodurans, disordered proteins, nudix hydrolase, desiccation effects, radiation-resistant} }
@article{article, author = {Awile, Omar and Kri\v{s}ko, Anita and Sbalzarini, Ivo and \v{Z}agrovi\'{c}, Bojan}, year = {2010}, pages = {1-10}, DOI = {10.1371/journal.pcbi.1000854}, keywords = {D. radiodurans, disordered proteins, nudix hydrolase, desiccation effects, radiation-resistant}, journal = {Plos computational biology}, doi = {10.1371/journal.pcbi.1000854}, volume = {6}, number = {7}, issn = {1553-734X}, title = {Intrinsically Disordered Regions May Lower the Hydration Free Energy in Proteins: A Case Study of Nudix Hydrolase in the Bacterium Deinococcus radiodurans}, keyword = {D. radiodurans, disordered proteins, nudix hydrolase, desiccation effects, radiation-resistant} }

Časopis indeksira:


  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


Citati:





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