NitrOFF: An Engineered Fluorescent Biosensor to Illuminate Nitrate Transport in Living Cells

M Mariah A. Cook (Department of Chemistry and Biochemistry The University of Texas at Dallas 800 West Campbell Road Richardson TX 75080 USA) J Jonathan D. Smailys (Department of Molecular Biosciences University of Texas 100 East 24th Street Austin TX 78712 USA) K Ke Ji S Shelby M. Phelps (Department of Chemistry and Biochemistry The University of Texas at Dallas 800 West Campbell Road Richardson TX 75080 USA) J Jasmine N. Tutol (Department of Chemistry and Biochemistry The University of Texas at Dallas 800 West Campbell Road Richardson TX 75080 USA) W Wantae Kim (McKetta Department of Chemical Engineering, 100 E. 24th Street, Austin, Texas 78712, United States) W Whitney S. Y. Ong (Department of Chemistry and Biochemistry, The University of Texas at Dallas) W Weicheng Peng C Caden Maydew (Department of Chemistry and Biochemistry The University of Texas at Dallas 800 West Campbell Road Richardson TX 75080 USA) Y Y. Jessie Zhang (Department of Molecular Biosciences and Oncology, University of Texas at Austin, 100 E. 24th Street, Austin, Texas 78712, United States) S Sheel C. Dodani (Department of Chemistry and Biochemistry, The University of Texas at Dallas)

Abstract

AbstractThe duality of nitrate is nowhere better exemplified than in human physiology—a detrimental pollutant but also a protective nutrient—particularly as connected to nitric oxide. Aside from limited insights into nitrate uptake and storage, foundational nitrate biology has lagged. Genetically encoded fluorescent biosensors can address this gap with real‐time imaging, but such technologies for mammalian cell applications remain rare. Here, we designed and engineered a biosensor fusing the green fluorescent protein EGFP and the nitrate recognition domain NreA from Staphylococcus carnosus. Seven rounds of directed evolution and 15 mutations resulted in NitrOFF. NitrOFF has a high degree of allosteric communication between the domains reflected in a turn‐off intensiometric response (Kd ≈ 9 µM). This was further reinforced by X‐ray crystal structures of apo and nitrate‐bound NitrOFF, which revealed a large‐scale conformational rearrangement changing the relative positioning of the domains by 68.4°. This dramatic difference was triggered by the formation of a long helix at the engineered linker connecting the two domains, peeling the β7 strand off the EGFP and thus extinguishing the fluorescence upon nitrate binding. Finally, we highlighted the utility of NitrOFF to monitor exogenous nitrate uptake and modulation in the human embryonic kidney (HEK) 293 cell line.

Article Details

Volume / Issue Vol. 64, Issue 40
Published September 26, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (11)

M

Mariah A. Cook

Department of Chemistry and Biochemistry The University of Texas at Dallas 800 West Campbell Road Richardson TX 75080 USA

J

Jonathan D. Smailys

Department of Molecular Biosciences University of Texas 100 East 24th Street Austin TX 78712 USA

K

Ke Ji

S

Shelby M. Phelps

Department of Chemistry and Biochemistry The University of Texas at Dallas 800 West Campbell Road Richardson TX 75080 USA

J

Jasmine N. Tutol

Department of Chemistry and Biochemistry The University of Texas at Dallas 800 West Campbell Road Richardson TX 75080 USA

W

Wantae Kim

McKetta Department of Chemical Engineering, 100 E. 24th Street, Austin, Texas 78712, United States

W

Whitney S. Y. Ong

Department of Chemistry and Biochemistry, The University of Texas at Dallas

W

Weicheng Peng

C

Caden Maydew

Department of Chemistry and Biochemistry The University of Texas at Dallas 800 West Campbell Road Richardson TX 75080 USA

Y

Y. Jessie Zhang

Department of Molecular Biosciences and Oncology, University of Texas at Austin, 100 E. 24th Street, Austin, Texas 78712, United States

S

Sheel C. Dodani

Department of Chemistry and Biochemistry, The University of Texas at Dallas