Glutamine Substitution at Lysine <sup>609</sup> in the Autoinhibitory Region Modulates Catalysis, Uncoupling, and Conformational Dynamics of Endothelial Nitric Oxide Synthase

Endothelial nitric oxide synthase (eNOS) is a critically important flavoheme enzyme that synthesizes nitric oxide (NO), a multifunctional signaling molecule essential to vascular homeostasis, immune modulation, and cardiovascular function. Post-translational modifications, such as acetylation, can affect eNOS activity by altering the charge state of lysine residues. However, we presently have little knowledge of how each lysine contributes to catalysis. In this study, we biochemically characterize two conserved lysine residues (Lys<sup>609</sup> and Lys<sup>733</sup>) of eNOS by employing lysine-to-glutamine substitutions (K609Q and K733Q), which neutralize the positive charge at these sites. The K609Q mutant showed an 80% increase in NO production and a better coupling efficiency (∼2.9 vs ∼5.2 in wild-type). This suggests that both electron transfer and enzymatic uncoupling were more effective. This mutant exhibited 1.5-fold enhanced cytochrome <i>c</i> reductase activity and accelerated flavin autoxidation, indicating an increased electron flux through the flavoprotein domain and decreased FMN semiquinone stability. Flavin fluorescence analysis further revealed that K609Q favors a partially open conformational equilibrium that supports enhanced interdomain electron transfer. Ferricyanide reduction remained unchanged across all variants, confirming that FAD-dependent electron transfer is unaffected and that the K609Q substitution specifically modulates FMN-mediated, not FAD-linked, electron flux. Conversely, K733Q exhibited wild-type-like behavior with little to no effect on coupling efficiency and catalysis. Our findings reveal that Lys<sup>609</sup> serves a regulatory function in eNOS catalysis. Substitution of this residue enhances coupling efficiency and promotes improved electron transfer. These insights advance our understanding of eNOS enzymology and indicate that the modulation of specific lysine residues, particularly Lys<sup>609</sup>, may aid in the preservation of endothelial NO production and alleviate the redox imbalance associated with endothelial dysfunction.

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Journal
ACS Omega
Published
2025-12-23
DOI
https://doi.org/10.1021/acsomega.5c09928
Primary Topic
Nitric Oxide and Endothelin Effects
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article
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article

Glutamine Substitution at Lysine 609 in the Autoinhibitory Region Modulates Catalysis, Uncoupling, and Conformational Dynamics of Endothelial Nitric Oxide Synthase

Daraksha Yameen, Rupesh Chaturvedi, Sajid Iqbal, Mohammad Masood et al.
ACS Omega
Nitric Oxide and Endothelin Effects
article

Glutamine Substitution at Lysine 609 in the Autoinhibitory Region Modulates Catalysis, Uncoupling, and Conformational Dynamics of Endothelial Nitric Oxide Synthase

Daraksha Yameen, Rupesh Chaturvedi, Sajid Iqbal, Mohammad Masood, Faizya Khan, Mohammad Mahfuzul Haque, Shadab Khan, Aleena Anwar, Anas Shamsi
article en

Abstract

Endothelial nitric oxide synthase (eNOS) is a critically important flavoheme enzyme that synthesizes nitric oxide (NO), a multifunctional signaling molecule essential to vascular homeostasis, immune modulation, and cardiovascular function. Post-translational modifications, such as acetylation, can affect eNOS activity by altering the charge state of lysine residues. However, we presently have little knowledge of how each lysine contributes to catalysis. In this study, we biochemically characterize two conserved lysine residues (Lys<sup>609</sup> and Lys<sup>733</sup>) of eNOS by employing lysine-to-glutamine substitutions (K609Q and K733Q), which neutralize the positive charge at these sites. The K609Q mutant showed an 80% increase in NO production and a better coupling efficiency (∼2.9 vs ∼5.2 in wild-type). This suggests that both electron transfer and enzymatic uncoupling were more effective. This mutant exhibited 1.5-fold enhanced cytochrome <i>c</i> reductase activity and accelerated flavin autoxidation, indicating an increased electron flux through the flavoprotein domain and decreased FMN semiquinone stability. Flavin fluorescence analysis further revealed that K609Q favors a partially open conformational equilibrium that supports enhanced interdomain electron transfer. Ferricyanide reduction remained unchanged across all variants, confirming that FAD-dependent electron transfer is unaffected and that the K609Q substitution specifically modulates FMN-mediated, not FAD-linked, electron flux. Conversely, K733Q exhibited wild-type-like behavior with little to no effect on coupling efficiency and catalysis. Our findings reveal that Lys<sup>609</sup> serves a regulatory function in eNOS catalysis. Substitution of this residue enhances coupling efficiency and promotes improved electron transfer. These insights advance our understanding of eNOS enzymology and indicate that the modulation of specific lysine residues, particularly Lys<sup>609</sup>, may aid in the preservation of endothelial NO production and alleviate the redox imbalance associated with endothelial dysfunction.

ACS OmegaVol. 11(1)
Jawaharlal Nehru University (IN), Ajman University (AE), University of Health and Allied Sciences (GH), Institute of Molecular Life Sciences (HU), Jamia Millia Islamia (IN)
Openalex Percentile: Top 34%
Nitric Oxide and Endothelin Effects
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