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Solving Kinetic Equations for the Laser Flash Photolysis Experiment on Nitric Oxide Synthases: Effect of Conformational Dynamics on the Interdomain Electron Transfer

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Journal J Phys Chem A
Specialty Chemistry
Date 2015 Oct 20
PMID 26477677
Citations 9
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Abstract

The production of nitric oxide by the nitric oxide synthase (NOS) enzyme depends on the interdomain electron transfer (IET) between the flavin mononucleotide (FMN) and heme domains. Although the rate of this IET has been measured by laser flash photolysis (LFP) for various NOS proteins, no rigorous analysis of the relevant kinetic equations was performed so far. In this work, we provide an analytical solution of the kinetic equations underlying the LFP approach. The derived expressions reveal that the bulk IET rate is significantly affected by the conformational dynamics that determines the formation and dissociation rates of the docking complex between the FMN and heme domains. We show that in order to informatively study the electron transfer across the NOS enzyme, LFP should be used in combination with other spectroscopic methods that could directly probe the docking equilibrium and the conformational change rate constants. The implications of the obtained analytical expressions for the interpretation of the LFP results from various native and modified NOS proteins are discussed. The mathematical formulas derived in this work should also be applicable for interpreting the IET kinetics in other modular redox enzymes.

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References
1.
Panda K, Ghosh S, Stuehr D . Calmodulin activates intersubunit electron transfer in the neuronal nitric-oxide synthase dimer. J Biol Chem. 2001; 276(26):23349-56. DOI: 10.1074/jbc.M100687200. View

2.
Poulos T . Heme enzyme structure and function. Chem Rev. 2014; 114(7):3919-62. PMC: 3981943. DOI: 10.1021/cr400415k. View

3.
Panda K, Adak S, Konas D, Sharma M, Stuehr D . A conserved aspartate (Asp-1393) regulates NADPH reduction of neuronal nitric-oxide synthase: implications for catalysis. J Biol Chem. 2004; 279(18):18323-33. DOI: 10.1074/jbc.M310391200. View

4.
Feng C, Roman L, Hazzard J, Ghosh D, Tollin G, Masters B . Deletion of the autoregulatory insert modulates intraprotein electron transfer in rat neuronal nitric oxide synthase. FEBS Lett. 2008; 582(18):2768-72. PMC: 2574637. DOI: 10.1016/j.febslet.2008.07.005. View

5.
Persechini A, Tran Q, Black D, Gogol E . Calmodulin-induced structural changes in endothelial nitric oxide synthase. FEBS Lett. 2012; 587(3):297-301. PMC: 3569036. DOI: 10.1016/j.febslet.2012.12.012. View