| Literature DB >> 28958937 |
Ghaith AlTawallbeh1, Mohammad M Haque2, Kiril A Streletzky3, Dennis J Stuehr2, Mekki Bayachou4.
Abstract
Endothelial nitric oxide synthase (eNOS) is a membrane-anchored enzyme. To highlight the potential role and effect of membrane phospholipids on the structure and activity of eNOS, we have incorporated the recombinant oxygenase subunit of eNOS into lipid nanodiscs. Two different size distribution modes were detected by multi-angle dynamic light scattering both for empty nanodiscs, and nanodiscs-bound eNOSoxy. The calculated hydrodynamic diameter for mode 1 species was 9.0 nm for empty nanodiscs and 9.8 nm for nanodisc bound eNOSoxy. Spectroscopic Griess assay was used to measure the enzymatic activity. Remarkably, the specific activity of nanodisc-bound eNOSoxy is ∼65% lower than the activity of free enzyme. The data shows that the nano-membrane environment affects the catalytic properties of eNOS heme domain.Entities:
Keywords: Enzyme activity; Membrane; Nanodisc; Nitric oxide; eNOS oxygenase domain
Mesh:
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Year: 2017 PMID: 28958937 PMCID: PMC5650499 DOI: 10.1016/j.bbrc.2017.09.131
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575