Nataly J. Arias
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Nataly J. Arias has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
- Ajit S. Divakaruni
Department of Molecular and Medical Pharmacology, University of California, Los Angeles, Los Angeles, CA 90095, USA
1 shared publication - Danielle L. Schmitt
Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California 90095, USA
1 shared publication - Edmund D. Kapelczak
Department of Molecular and Medical Pharmacology, University of California, Los Angeles, CA 90095, USA
1 shared publication - Jack M. Scully
Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California 90095, USA
1 shared publication - Katie G. Vineall
Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California 90095
1 shared publication Michael J. Sun
Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California 90095
1 shared publication
Latest Publications
- Open Access
Illuminating spatial dynamics of glutamine metabolism with a sensitive genetically encoded biosensor
Glutamine is the most abundant amino acid in serum, used as a key nutrient by cells for protein synthesis, energy production, carbon and nitrogen metabolism, and cellular redox balance. The use of glutamine in the cell is highly compartmentalized, but the dynamics of glutamine metabolism across organelles and individual cells are not fully understood. To illuminate subcellular glutamine dynamics, we developed a green fluorescent protein-based intracellular glutamine optical reporter, iGlo. We find iGlo is sensitive and specific for glutamine and can be used to measure glutamine uptake, production, and consumption with high spatiotemporal resolution in multiple cell types. Furthermore, multiplexed imaging of iGlo with a lactate biosensor in single cells reveals the temporal crosstalk between glucose and glutamine metabolism to maintain energy homeostasis. Thus, iGlo enables the sensitive and precise study of compartmentalized glutamine dynamics and represents a new and enhanced tool for studying the spatiotemporal dynamics and regulation of metabolism.
Open AccessIlluminating spatial dynamics of glutamine metabolism with a sensitive genetically encoded biosensor
Glutamine is the most abundant amino acid in serum, used as a key nutrient by cells for protein synthesis, energy production, carbon and nitrogen metabolism, and cellular redox balance. The use of glutamine in the cell is highly compartmentalized, but the dynamics of glutamine metabolism across organelles and individual cells are not fully understood. To illuminate subcellular glutamine dynamics, we developed a green fluorescent protein-based intracellular glutamine optical reporter, iGlo. We find iGlo is sensitive and specific for glutamine and can be used to measure glutamine uptake, production, and consumption with high spatiotemporal resolution in multiple cell types. Furthermore, multiplexed imaging of iGlo with a lactate biosensor in single cells reveals the temporal crosstalk between glucose and glutamine metabolism to maintain energy homeostasis. Thus, iGlo enables the sensitive and precise study of compartmentalized glutamine dynamics and represents a new and enhanced tool for studying the spatiotemporal dynamics and regulation of metabolism.