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Diversity in Overall Activity Regulation of Ribonucleotide Reductase
Umeå universitet, Medicinska fakulteten, Institutionen för medicinsk kemi och biofysik. (Anders Hofer)
Umeå universitet, Medicinska fakulteten, Institutionen för medicinsk kemi och biofysik. (Anders Hofer)
Vise andre og tillknytning
2015 (engelsk)Inngår i: Journal of Biological Chemistry, ISSN 0021-9258, E-ISSN 1083-351X, Vol. 290, nr 28, s. 17339-17348Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Ribonucleotide reductase (RNR) catalyzes the reduction of ribonucleotides to the corresponding deoxyribonucleotides, which are used as building blocks for DNA replication and repair. This process is tightly regulated via two allosteric sites, the specificity site (s-site) and the overall activity site (a-site). The a-site resides in an N-terminal ATP cone domain that binds dATP or ATP and functions as an on/off switch, whereas the composite s-site binds ATP, dATP, dTTP, or dGTP and determines which substrate to reduce. There are three classes of RNRs, and class I RNRs consist of different combinations of α and β subunits. In eukaryotic and Escherichia coli class I RNRs, dATP inhibits enzyme activity through the formation of inactive α6 and α4β4 complexes, respectively. Here we show that the Pseudomonas aeruginosa class I RNR has a duplicated ATP cone domain and represents a third mechanism of overall activity regulation. Each α polypeptide binds three dATP molecules, and the N-terminal ATP cone is critical for binding two of the dATPs because a truncated protein lacking this cone could only bind dATP to its s-site. ATP activates the enzyme solely by preventing dATP from binding. The dATP-induced inactive form is an α4 complex, which can interact with β2 to form a non-productive α4β2 complex. Other allosteric effectors induce a mixture of α2 and α4 forms, with the former being able to interact with β2 to form active α2β2 complexes. The unique features of the P. aeruginosa RNR are interesting both from evolutionary and drug discovery perspectives.

sted, utgiver, år, opplag, sider
2015. Vol. 290, nr 28, s. 17339-17348
HSV kategori
Identifikatorer
URN: urn:nbn:se:umu:diva-109543DOI: 10.1074/jbc.M115.649624ISI: 000357730900029PubMedID: 25971975OAI: oai:DiVA.org:umu-109543DiVA, id: diva2:857888
Forskningsfinansiär
Swedish Research CouncilThe Kempe FoundationsCarl Tryggers foundation Tilgjengelig fra: 2015-09-30 Laget: 2015-09-30 Sist oppdatert: 2018-06-07bibliografisk kontrollert
Inngår i avhandling
1. Class I Ribonucleotide Reductases: overall activity regulation, oligomerization, and drug targeting
Åpne denne publikasjonen i ny fane eller vindu >>Class I Ribonucleotide Reductases: overall activity regulation, oligomerization, and drug targeting
2017 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Ribonucleotide reductase (RNR) is a key enzyme in the de novo biosynthesis and homeostatic maintenance of all four DNA building blocks by being able to make deoxyribonucleotides from the corresponding ribonucleotides. It is important for the cell to control the production of a balanced supply of the dNTPs to minimize misincorporations in DNA. Because RNR is the rate-limiting enzyme in DNA synthesis, it is an important target for antimicrobial and antiproliferative molecules. The enzyme RNR has one of the most sophisticated allosteric regulations known in Nature with four allosteric effectors (ATP, dATP, dGTP, and dTTP) and two allosteric sites. One of the sites (s-site) controls the substrate specificity of the enzyme, whereas the other one (a-site) regulates the overall activity.  The a-site binds either dATP, which inhibits the enzyme or ATP that activates the enzyme. In eukaryotes, ATP activation is directly through the a-site and in E. coli it is a cross-talk effect between the a and s-sites. It is important to study and get more knowledge about the overall activity regulation of RNR, both because it has an important physiological function, but also because it may provide important clues to the design of antibacterial and antiproliferative drugs, which can target RNR.

Previous studies of class I RNRs, the class found in nearly all eukaryotes and many prokaryotes have revealed that the overall activity regulation is dependent on the formation of oligomeric complexes. The class I RNR consists of two subunits, a large α subunit, and a small β subunit. The oligomeric complexes vary between different species with the mammalian and yeast enzymes cycle between structurally different active and inactive α6β2 complexes, and the E. coli enzyme cycles between active α2β2 and inactive α4β4 complexes. Because RNR equilibrates between many different oligomeric forms that are not resolved by most conventional methods, we have used a technique termed gas-phase electrophoretic macromolecule analysis (GEMMA). In the present studies, our focus is on characterizing both prokaryotic and mammalian class I RNRs. In one of our projects, we have studied the class I RNR from Pseudomonas aeruginosa and found that it represents a novel mechanism of overall activity allosteric regulation, which is different from the two known overall activity allosteric regulation found in E. coli and eukaryotic RNRs, respectively.  The structural differences between the bacterial and the eukaryote class I RNRs are interesting from a drug developmental viewpoint because they open up the possibility of finding inhibitors that selectively target the pathogens. The biochemical data that we have published in the above project was later supported by crystal structure and solution X-ray scattering data that we published together with Derek T. Logan`s research group.

We have also studied the effect of a novel antiproliferative molecule, NSC73735, on the oligomerization of the human RNR large subunit. This collaborative research results showed that the molecule NSC73735 is the first reported non-nucleoside molecule which alters the oligomerization to inhibit human RNR and the molecule disrupts the cell cycle distribution in human leukemia cells.

sted, utgiver, år, opplag, sider
Umeå: Umeå universitet, 2017. s. 51+8
Serie
Umeå University medical dissertations, ISSN 0346-6612 ; 1894
Emneord
Ribonucleotide reductase, GEMMA, Allosteric regulation
HSV kategori
Forskningsprogram
medicinsk biokemi
Identifikatorer
urn:nbn:se:umu:diva-133817 (URN)978-91-7601-703-6 (ISBN)
Disputas
2017-05-12, KB.E3.01 Lilla Hörsalen, KBC huset, Umeå, 09:00 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2017-04-21 Laget: 2017-04-18 Sist oppdatert: 2018-06-09bibliografisk kontrollert

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