The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Phosphotransfer networks and cellular energetics
Open accessAbstract
SUMMARY: Precise coupling of spatially separated intracellular ATP-producing and ATP-consuming processes is fundamental to the bioenergetics of living organisms, ensuring a fail-safe operation of the energetic system over a broad range of cellular functional activities. Here, we provide an overview of the role of spatially arranged enzymatic networks, catalyzed by creatine kinase,adenylate kinase, carbonic anhydrase and glycolytic enzymes, in efficient high-energy phosphoryl transfer and signal communication in the cell. Studies of transgenic creatine kinase and adenylate kinase deficient mice, along with pharmacological targeting of individual enzymes, have revealed the importance of near-equilibrium reactions in the dissipation of metabolite gradients and communication of energetic signals to distinct intracellular compartments,including the cell nucleus and membrane metabolic sensors. Enzymatic capacities, isoform distribution and the dynamics of net phosphoryl flux through the integrated phosphotransfer systems tightly correlate with cellular functions, indicating a critical role of such networks in efficient energy transfer and distribution, thereby securing the cellular economy and energetic homeostasis under stress.
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Cites
Coupling of Cell Energetics with Membrane Metabolic Sensing
Abraham, M. R., Selivanov, V. A., Hodgson, D. M., Pucar, D., Zingman, L. V., Wieringa, B., Dzeja, P. P., Alekseev, A. E., & Terzic, A. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m201777200 · Cited by 148
Self-citationRole of MgADP in the development of diastolic dysfunction in the intact beating rat heart
Tian, R., Christe, M. E., Spindler, M., Hopkins, J. C., Halow, J. M., Camacho, S. A., & Ingwall, J. S. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119220 · Cited by 103
Cited by
Use of Cells Expressing γ Subunit Variants to Identify Diverse Mechanisms of AMPK Activation
Hawley, S. A., Ross, F. A., Chevtzoff, C., Green, K. A., Evans, A., Fogarty, S., Towler, M. C., Brown, L. J., Ogunbayo, O. A., Evans, A. M., et al. (2010) · Cell Metabolism · doi:10.1016/j.cmet.2010.04.001 · Cited by 773
Bonora, M., Patergnani, S., Rimessi, A., De Marchi, E., Suski, J. M., Bononi, A., Giorgi, C., Marchi, S., Missiroli, S., Poletti, F., et al. (2012) · Purinergic Signalling · doi:10.1007/s11302-012-9305-8 · Cited by 644
Energy metabolism in heart failure
Ventura‐Clapier, R., Garnier, A., & Veksler, V. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2003.055095 · Cited by 499
ATP flux through creatine kinase in the normal, stressed, and failing human heart
Weiss, R. G., Gerstenblith, G., & Bottomley, P. A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408962102 · Cited by 350
Nitric Oxide as a Unique Bioactive Signaling Messenger in Physiology and Pathophysiology
Tuteja, N., Chandra, M., Tuteja, R., & Misra, M. K. (2004) · BioMed Research International · doi:10.1155/s1110724304402034 · Cited by 269
Metadata
- Authors
- Dzeja, P. P., & Terzic, A.
- Venue
- Journal of Experimental Biology
- Publisher
- The Company of Biologists
- Published
- 2003-06-15
- Volume
- 206
- Issue
- 12
- Pages
- 2039-2047
- ISSN
- 0022-0949 (ISSN-L)
- 1477-9145
- OpenAlex
- W2150994390
- Cited by
- 471
- References
- 2
- FWCI
- 7.29
- Type
- journal article
- Language
- en
- Open access
- bronze
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