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Pregled bibliografske jedinice broj: 1139441

Mitochondrial Uncoupling Proteins (UCP1-UCP3) and Adenine Nucleotide Translocase (ANT1) Enhance the Protonophoric Action of 2,4-Dinitrophenol in Mitochondria and Planar Bilayer Membranes


Žuna, Kristina; Jovanović, Olga; Khailova, Ljudmila S.; Škulj, Sanja; Brkljača, Zlatko; Kreiter, Jürgen; Kotova, Elena A.; Vazdar, Mario; Antonenko, Yuri N.; Pohl, Elena E.
Mitochondrial Uncoupling Proteins (UCP1-UCP3) and Adenine Nucleotide Translocase (ANT1) Enhance the Protonophoric Action of 2,4-Dinitrophenol in Mitochondria and Planar Bilayer Membranes // Biomolecules, 11 (2021), 1178-1192 doi:10.3390/biom11081178 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 1139441 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Mitochondrial Uncoupling Proteins (UCP1-UCP3) and Adenine Nucleotide Translocase (ANT1) Enhance the Protonophoric Action of 2,4-Dinitrophenol in Mitochondria and Planar Bilayer Membranes

Autori
Žuna, Kristina ; Jovanović, Olga ; Khailova, Ljudmila S. ; Škulj, Sanja ; Brkljača, Zlatko ; Kreiter, Jürgen ; Kotova, Elena A. ; Vazdar, Mario ; Antonenko, Yuri N. ; Pohl, Elena E.

Izvornik
Biomolecules (2218-273X) 11 (2021); 1178-1192

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

Ključne riječi
mitochondrial uncoupler ; protonophore ; membrane potential ; proton conductance ; artificial membranes ; molecular dynamics simulations

Sažetak
2, 4-Dinitrophenol (DNP) is a classic uncoupler of oxidative phosphorylation in mitochondria which is still used in “diet pills”, despite its high toxicity and lack of antidotes. DNP increases the proton current through pure lipid membranes, similar to other chemical uncouplers. However, the molecular mechanism of its action in the mitochondria is far from being understood. The sensitivity of DNP’s uncoupling action in mitochondria to carboxyatractyloside, a specific inhibitor of adenine nucleotide translocase (ANT), suggests the involvement of ANT and probably other mitochondrial proton-transporting proteins in the DNP’s protonophoric activity. To test this hypothesis, we investigated the contribution of recombinant ANT1 and the uncoupling proteins UCP1- UCP3 to DNP-mediated proton leakage using the well-defined model of planar bilayer lipid membranes. All four proteins significantly enhanced the protonophoric effect of DNP. Notably, only long-chain free fatty acids were previously shown to be co-factors of UCPs and ANT1. Using site-directed mutagenesis and molecular dynamics simulations, we showed that arginine 79 of ANT1 is crucial for the DNP-mediated increase of membrane conductance, implying that this amino acid participates in DNP binding to ANT1.

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)



POVEZANOST RADA


Projekti:
HRZZ-IP-2019-04-3804 - Prijenos tvari kroz biološke membrane potpomognut proteinima (ProtBioMemb) (Vazdar, Mario, HRZZ - 2019-04) ( CroRIS)

Ustanove:
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Zagreb

Profili:

Avatar Url Mario Vazdar (autor)

Avatar Url Zlatko Brkljača (autor)

Avatar Url Sanja Škulj (autor)

Poveznice na cjeloviti tekst rada:

doi www.mdpi.com doi.org fulir.irb.hr

Citiraj ovu publikaciju:

Žuna, Kristina; Jovanović, Olga; Khailova, Ljudmila S.; Škulj, Sanja; Brkljača, Zlatko; Kreiter, Jürgen; Kotova, Elena A.; Vazdar, Mario; Antonenko, Yuri N.; Pohl, Elena E.
Mitochondrial Uncoupling Proteins (UCP1-UCP3) and Adenine Nucleotide Translocase (ANT1) Enhance the Protonophoric Action of 2,4-Dinitrophenol in Mitochondria and Planar Bilayer Membranes // Biomolecules, 11 (2021), 1178-1192 doi:10.3390/biom11081178 (međunarodna recenzija, članak, znanstveni)
Žuna, K., Jovanović, O., Khailova, L., Škulj, S., Brkljača, Z., Kreiter, J., Kotova, E., Vazdar, M., Antonenko, Y. & Pohl, E. (2021) Mitochondrial Uncoupling Proteins (UCP1-UCP3) and Adenine Nucleotide Translocase (ANT1) Enhance the Protonophoric Action of 2,4-Dinitrophenol in Mitochondria and Planar Bilayer Membranes. Biomolecules, 11, 1178-1192 doi:10.3390/biom11081178.
@article{article, author = {\v{Z}una, Kristina and Jovanovi\'{c}, Olga and Khailova, Ljudmila S. and \v{S}kulj, Sanja and Brklja\v{c}a, Zlatko and Kreiter, J\"{u}rgen and Kotova, Elena A. and Vazdar, Mario and Antonenko, Yuri N. and Pohl, Elena E.}, year = {2021}, pages = {1178-1192}, DOI = {10.3390/biom11081178}, keywords = {mitochondrial uncoupler, protonophore, membrane potential, proton conductance, artificial membranes, molecular dynamics simulations}, journal = {Biomolecules}, doi = {10.3390/biom11081178}, volume = {11}, issn = {2218-273X}, title = {Mitochondrial Uncoupling Proteins (UCP1-UCP3) and Adenine Nucleotide Translocase (ANT1) Enhance the Protonophoric Action of 2,4-Dinitrophenol in Mitochondria and Planar Bilayer Membranes}, keyword = {mitochondrial uncoupler, protonophore, membrane potential, proton conductance, artificial membranes, molecular dynamics simulations} }
@article{article, author = {\v{Z}una, Kristina and Jovanovi\'{c}, Olga and Khailova, Ljudmila S. and \v{S}kulj, Sanja and Brklja\v{c}a, Zlatko and Kreiter, J\"{u}rgen and Kotova, Elena A. and Vazdar, Mario and Antonenko, Yuri N. and Pohl, Elena E.}, year = {2021}, pages = {1178-1192}, DOI = {10.3390/biom11081178}, keywords = {mitochondrial uncoupler, protonophore, membrane potential, proton conductance, artificial membranes, molecular dynamics simulations}, journal = {Biomolecules}, doi = {10.3390/biom11081178}, volume = {11}, issn = {2218-273X}, title = {Mitochondrial Uncoupling Proteins (UCP1-UCP3) and Adenine Nucleotide Translocase (ANT1) Enhance the Protonophoric Action of 2,4-Dinitrophenol in Mitochondria and Planar Bilayer Membranes}, keyword = {mitochondrial uncoupler, protonophore, membrane potential, proton conductance, artificial membranes, molecular dynamics simulations} }

Časopis indeksira:


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


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