The objective of this proposal is to elucidate how glucose metabolism (i.e. glycolysis and gluconeogenesis) and mitochondrial metabolism are spatially and functionally (spatiofunctionally) interconnected and dynamically orchestrated in human living cells. Current understanding of the highly enmeshed web of metabolic pathways has been limited in 2D, but cellular metabolism takes place in space and time (i.e. 4D). A number of metabolic pathways are spatially confined into either membrane-bound organelles or membraneless compartments. To understand how metabolic pathways are regulated and networked, it is vital to know how organelles or membraneless compartments are spatially arranged and functionally interplay in 4D. We have recently reported that the cytoplasmic, rate-determining enzymes in glucose metabolism are spatially organized into membraneless compartments in various sizes in human cells. We proposed that they shunt glucose flux to anabolic biosynthetic pathways. More importantly, our preliminary results suggest now that the enzyme compartments, formed by liquid-liquid phase separation (LLPS), might be spatially and functionally linked with mitochondria. Thus, in this proposal, we hypothesize that the enzyme compartments in glucose metabolism are spatially and functionally associated with mitochondria in 4D, by which LLSP plays a role to adapt cellular demands. .We will characterize precise mechanisms of the formation and modulation of the enzyme compartments. In addition, we will reveal how the enzyme compartments of glucose metabolism are functionally and spatially coordinated with the mitochondria and the regulatory mechanisms of their network in living cells. The proposed work will offer new, powerful 4D imaging and analysis approaches to explore novel perspectives of spatiotemporal dynamics of metabolic networks inside cells. This work will provide the fundamental principle of understanding the new class of essential organelles in the cell and will provide a new paradigm to comprehend 4-D map of metabolic networks in living cells.

Public Health Relevance

4D functional mapping of glucose metabolism in Living Cells Narrative Metabolic pathways take place in 3-dimensional space and time (i.e. 4 dimensions (4D)), but our current understanding is limited by 2D networks of metabolic pathways. We envision that the proposed research will provide unprecedented insights of how glucose metabolism (i.e. glycolysis and gluconeogenesis) and mitochondrial metabolism are spatially and functionally (spatiofunctionally) interconnected and dynamically orchestrated in human living cells. Therefore, the proposed research will significantly advance our understanding of 4 dimensional metabolic network of glucose metabolism with mitochondria and its dysregulation in human metabolic diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM134086-02
Application #
9967050
Study Section
Molecular and Cellular Endocrinology Study Section (MCE)
Program Officer
Barski, Oleg
Project Start
2019-07-01
Project End
2024-06-30
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
2
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Maryland Balt CO Campus
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
061364808
City
Baltimore
State
MD
Country
United States
Zip Code
21250