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Calmodulin activates neuronal nitric oxide synthase by enabling transitions between conformational states.
- Source :
-
FEBS letters [FEBS Lett] 2013 Jan 04; Vol. 587 (1), pp. 44-7. Date of Electronic Publication: 2012 Nov 15. - Publication Year :
- 2013
-
Abstract
- We recently showed that inducible nitric oxide synthase conformational intermediates can be resolved via FMN fluorescence lifetimes. Here we show that neuronal NOS activation by calmodulin removes constraints favoring a closed 'input state', increasing occupation of other states and facilitating conformational transitions. The 90 ps FMN input state lifetime distinguishes it from ∼4 ns 'open' states in which FMN does not interact strongly with other groups, or 0.9 ns output states in which FMN interacts with ferriheme. Enablement of the conformational cycle is an important paradigm for control in nNOS and related enzymes, and may extend to other control modalities.<br /> (Copyright © 2012. Published by Elsevier B.V.)
- Subjects :
- Algorithms
Binding Sites
Calmodulin chemistry
Enzyme Activation
Flavin Mononucleotide metabolism
Hemin metabolism
Holoenzymes chemistry
Holoenzymes genetics
Holoenzymes metabolism
Humans
Kinetics
Mutant Proteins chemistry
Mutant Proteins metabolism
Nitric Oxide Synthase Type I chemistry
Nitric Oxide Synthase Type I genetics
Protein Conformation
Protein Interaction Domains and Motifs
Recombinant Proteins chemistry
Recombinant Proteins metabolism
Spectrometry, Fluorescence
Calmodulin metabolism
Nitric Oxide Synthase Type I metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3468
- Volume :
- 587
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- FEBS letters
- Publication Type :
- Academic Journal
- Accession number :
- 23159936
- Full Text :
- https://doi.org/10.1016/j.febslet.2012.10.039