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10.1074/jbc.REV120.013746

http://scihub22266oqcxt.onion/10.1074/jbc.REV120.013746
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suck abstract from ncbi


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pmid32737197      J+Biol+Chem 2020 ; 295 (39): 13432-13443
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  • Mechanistic cross-talk between DNA/RNA polymerase enzyme kinetics and nucleotide substrate availability in cells: Implications for polymerase inhibitor discovery #MMPMID32737197
  • Coggins SA; Mahboubi B; Schinazi RF; Kim B
  • J Biol Chem 2020[Sep]; 295 (39): 13432-13443 PMID32737197show ga
  • Enzyme kinetic analysis reveals a dynamic relationship between enzymes and their substrates. Overall enzyme activity can be controlled by both protein expression and various cellular regulatory systems. Interestingly, the availability and concentrations of intracellular substrates can constantly change, depending on conditions and cell types. Here, we review previously reported enzyme kinetic parameters of cellular and viral DNA and RNA polymerases with respect to cellular levels of their nucleotide substrates. This broad perspective exposes a remarkable co-evolution scenario of DNA polymerase enzyme kinetics with dNTP levels that can vastly change, depending on cell proliferation profiles. Similarly, RNA polymerases display much higher K(m) values than DNA polymerases, possibly due to millimolar range rNTP concentrations found in cells (compared with micromolar range dNTP levels). Polymerases are commonly targeted by nucleotide analog inhibitors for the treatments of various human diseases, such as cancers and viral pathogens. Because these inhibitors compete against natural cellular nucleotides, the efficacy of each inhibitor can be affected by varying cellular nucleotide levels in their target cells. Overall, both kinetic discrepancy between DNA and RNA polymerases and cellular concentration discrepancy between dNTPs and rNTPs present pharmacological and mechanistic considerations for therapeutic discovery.
  • |*Drug Discovery[MESH]
  • |Animals[MESH]
  • |DNA-Directed DNA Polymerase/*metabolism[MESH]
  • |DNA-Directed RNA Polymerases/*antagonists & inhibitors/metabolism[MESH]
  • |Enzyme Inhibitors/*pharmacology[MESH]
  • |Humans[MESH]
  • |Kinetics[MESH]
  • |Nucleotides/*metabolism[MESH]


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